Prof. ZEYNEP ŞIKLAR

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

Adrenal hypoandrogenism in adolescents with premature ovarian insufficiency

Bilici M. E., ŞIKLAR Z., Cetinkaya S., ÖZSU E., AYCAN Z., BERBEROĞLU M.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , 2025 (SCI-Expanded)

Congenital Adrenal Hyperplasia and Adrenal Insufficiency in Children: An Evidence-based Review with Good Practice Points by Adrenal Working Group of The Turkish Society for Pediatric Endocrinology and Diabetes

ŞIKLAR Z.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , pp.1-2, 2025 (SCI-Expanded)

Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Gunes S. O., Kendirci H. N. P., Unal E., Bulus A. D., DÜNDAR İ., ŞIKLAR Z.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , pp.3-11, 2025 (SCI-Expanded)

Treatment and Follow-up of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Childhood and Adolescence

Kendirci H. N. P., Unal E., DÜNDAR İ., Bulus A. D., Gunes S. O., ŞIKLAR Z.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , pp.12-22, 2025 (SCI-Expanded)

Unraveling the Genetic Puzzle: Could MAP3K7 Be a Candidate Gene for RASopathies? Case Presentation.

Kizilcan Cetin S., Siklar Z., Aycan Z., Ozsu E., Ceylaner S., Berberoğlu M.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

Evaluation of Growth Characteristics and Final Heights of Cases Diagnosed with Noonan Syndrome on GH Treatment.

Şıklar Z., Berberoğlu M., Kızılcan Çetin S., Yıldız M., Turan S., Darcan Ş., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

A real-world data analysis of 37 pediatric patients with pheochromocytoma and paraganglioma: Evaluation of the concordance between current diagnostic and treatment algorithms and clinical management practices in resource-limited settings

Kurt I., GÜRPINAR TOSUN B., Uslu N. G., ÖZALP KIZILAY D., Dikmen I., Comlek F. O., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.475, 2024 (SCI-Expanded)

Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study.

Şıklar Z., Özsu E., Kızılcan Çetin S., Özen S., Çizmecioğlu-Jones F., Balkı H. G., et al.

Journal of clinical research in pediatric endocrinology , vol.16, no.3, pp.288-296, 2024 (SCI-Expanded)

Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.

Özsu E., Çetinkaya S., Bolu S., Hatipoğlu N., Savaş Erdeve Ş., Evliyaoğlu O., et al.

Journal of clinical research in pediatric endocrinology , vol.16, no.3, pp.297-305, 2024 (SCI-Expanded)

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Ozer Y., Anik A., SAYILI U., Tercan U., Sevim R. D., Gunes S., et al.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.47, no.9, pp.2213-2224, 2024 (SCI-Expanded)

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

ŞIKLAR Z., ÇAMTOSUN E., Bolu S., Yildiz M., AKINCI A., Bas F., et al.

ENDOCRINE , vol.85, no.3, pp.1407-1416, 2024 (SCI-Expanded)

Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis.

Şen E. K., Berberoğlu M., Şenyazar G., Kızılcan Çetin S., Ceran A., Erişen Karaca S., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

Evaluation of quality of life in children with precocious puberty

YILMAZER İ. N., Abseyi S. N., Senyazar G., BERBEROĞLU M., ŞIKLAR Z., AYCAN Z.

CLINICAL ENDOCRINOLOGY , no.4, pp.338-342, 2024 (SCI-Expanded)

Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome.

Kızılcan Çetin S., Özsu E., Şıklar Z., Çakmaklı H. F., Şenyazar G., Aycan Z., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline RET S891A Protooncogene Mutation: 7-Year Follow-up with Successful Sorafenib Treatment.

Kizilcan Cetin S., Siklar Z., Ozsu E., Ceran A., Ceyhan K., Aycan Z., et al.

Journal of clinical research in pediatric endocrinology , 2023 (SCI-Expanded)

A Challenging Case of Ectopic ACTH Syndrome with Bronchial Carcinoid and Literature Review

Abseyi N., Şıklar Z., Özsu E., Kayı Cangır A., Ünal E., Taçyıldız N., et al.

JCRPE JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.6, pp.6-7, 2023 (SCI-Expanded)

Clinic Heterogeneity and Management of Pediatric Patients With Germline RET Proto-oncogene Mutation: Single-center Experience

ŞIKLAR Z., Kontbay T., Dincaslan H., ÜNAL E., BERBEROĞLU M.

Journal of pediatric hematology/oncology , vol.45, no.7, 2023 (SCI-Expanded)

Central Precocious Puberty in Boys; Diagnosis, Treatment and Follow-up: A Nation-Wide Study

Gunes S. O., Sakar M., Sahin N. M., KARAGÜZEL G., CİMBEK E. A., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , pp.363-364, 2023 (SCI-Expanded)

Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia

Isik R. O., Kızılcan Çetin S., Cetinkaya S., Berberoğlu M., Şıklar Z., Özsu E., et al.

Clinical Endocrinology , vol.99, no.2, pp.135-141, 2023 (SCI-Expanded)

Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases.

Şıklar Z., Kontbay T., Colclough K., Patel K. A., Berberoğlu M.

Journal of clinical research in pediatric endocrinology , vol.15, pp.90-96, 2023 (SCI-Expanded)

Evaluation of Abnormal Uterine Bleeding in Adolescents: Single Center Experience.

Kızılcan Çetin S., Aycan Z., Özsu E., Şıklar Z., Ceran A., Erişen Karaca S., et al.

Journal of clinical research in pediatric endocrinology , 2023 (SCI-Expanded)

Mitotically Active Follicular Nodule in Early Childhood: A Case Report with A Novel Mutation in the Thyroglobulin Gene.

Kizilcan Cetin S., Aycan Z., Siklar Z., Dizbay Sak S., Ceylaner S., Ozsu E., et al.

Journal of clinical research in pediatric endocrinology , 2022 (SCI-Expanded)

The Effect of Growth Hormone Therapy on Cardiac Outcomes in Noonan Syndrome: Long Term Follow-up Results

Cetin S., RAMOĞLU M. G., ŞIKLAR Z., ÖZSU E., AYCAN Z., Tutar H. E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.4, pp.422-432, 2022 (SCI-Expanded)

Clinical Features, Risk Classifications and Long-Term Follow Up Of Childhood Differentiated Thyroid Cancer (DTC): A Single Reference-Center Experience

AYCAN Z., Cetin S. K., ŞIKLAR Z., ÖZSU E., Fitoz S., CEYHAN K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.95, no.SUPPL 2, pp.414, 2022 (SCI-Expanded)

Hyperprolactinemia in children and adolescents and long-term follow-up results of prolactinoma cases: a single-centre experience

Kontbay T., ŞIKLAR Z., ÖZSU E., Uyanik R., Bilici E., CERAN A., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.64, no.5, pp.892-899, 2022 (SCI-Expanded)

Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment

Kontbay T., ŞIKLAR Z., Ceylaner S., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.3, pp.356-360, 2022 (SCI-Expanded)

Evaluation of the etiological and clinical characteristics of pediatric central diabetes insipidus

Gasimova E., BERBEROĞLU M., ÖZSU CAVGA E., AYCAN Z., Uyanik R., Bilici E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.35, no.8, pp.1089-1096, 2022 (SCI-Expanded) Sustainable Development

Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?

Tas O., Kontbay T., DOĞAN Ö., KÖSE E., BERBEROĞLU M., ŞIKLAR Z., et al.

KLINISCHE PADIATRIE , vol.234, no.4, pp.221-227, 2022 (SCI-Expanded) Sustainable Development

Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism

GÜNAY F., ŞIKLAR Z., BERBEROĞLU M.

TURKISH JOURNAL OF PEDIATRICS , vol.64, no.3, pp.490-499, 2022 (SCI-Expanded)

Adaptation Study of the Newest Vital Sign on Adolescents With Type 1 Diabetes and Healthy Adolescents in Turkish

GÜMÜŞ A. B., KESER A., ŞIKLAR Z., BERBEROĞLU M.

TOPICS IN CLINICAL NUTRITION , vol.37, no.2, pp.142-153, 2022 (SCI-Expanded) Sustainable Development

Correction: Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?

Taş Ö., Kontbay T., Dogan Ö., Kose E., Berberoglu M., Siklar Z., et al.

Klinische Padiatrie , 2022 (SCI-Expanded)

Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

Patel K. A., Ozbek M. N., Yildiz M., GÜRAN T., Kocyigit C., Acar S., et al.

DIABETOLOGIA , vol.65, pp.336-342, 2022 (SCI-Expanded) Sustainable Development

Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children

AKDUMAN F., ŞIKLAR Z., ÖZSU E., DOĞAN Ö., KIR K. M., BERBEROĞLU M.

JCRPE JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.14, no.4, pp.433-443, 2022 (SCI-Expanded)

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

Goksen D., Yesilkaya E., ÖZEN S., Kor Y., EREN E., Korkmaz O., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.13, no.4, pp.433-438, 2021 (SCI-Expanded)

Determining the risk of diabulimia and its relationship with diet quality and nutritional status of adolescents with type 1 diabetes Déterminer le risque de diaboulimie et sa relation avec la qualité de l'alimentation et l’état nutritionnel des adolescents atteints de diabète de type 1

ŞAHİN BODUR G., KESER A., ŞIKLAR Z., BERBEROĞLU M.

Nutrition Clinique et Metabolisme , vol.35, no.4, pp.281-287, 2021 (SCI-Expanded) Sustainable Development

Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A single-center experience

Cetin S. K., ŞIKLAR Z., ÖZSU CAVGA E., AYCAN Z., CERAN A., Karaca S. E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.94, no.SUPPL 1, pp.222, 2021 (SCI-Expanded)

Evaluation of Admission Characteristics, Treatment and Follow-up Findings of Children with Primary Osteoporosis

Cetin S. K., ŞIKLAR Z., AYCAN Z., ÖZSU CAVGA E., CERAN A., Senyazar G., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.94, no.SUPPL 1, pp.212, 2021 (SCI-Expanded)

The impact of high-fat and high-protein meal of adolescents with type 1 diabetes mellitus receiving intensive insulin therapy on postprandial blood glucose level: a randomized, crossover, breakfast study

Gumus A. B., KESER A., ŞIKLAR Z., BERBEROĞLU M.

INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES , vol.41, no.2, pp.249-258, 2021 (SCI-Expanded) Sustainable Development

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Savas-Erdeve S., AYCAN Z., Cetinkaya S., Ozturk A. P., BAŞ F., Poyrazoglu S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.13, no.2, pp.180-186, 2021 (SCI-Expanded)

Cardiac phenotype in familial partial lipodystrophy

Eldin A. J., Akinci B., da Rocha A. M., Meral R., YILDIRIM ŞİMŞİR I., ADIYAMAN S. C., et al.

CLINICAL ENDOCRINOLOGY , vol.94, no.6, pp.1043-1053, 2021 (SCI-Expanded)

Managing precocious puberty: A necessity for psychiatric evaluation

Temelturk R. D., Ekici G. I., Beberoglu M., ŞIKLAR Z., KILIÇ B. G.

ASIAN JOURNAL OF PSYCHIATRY , vol.58, 2021 (SCI-Expanded)

Does obesity influence ventricular repolarisation in children?

Yildirim Yildiz N., UÇAR T., RAMOĞLU M. G., BERBEROĞLU M., ŞIKLAR Z., Tutar E., et al.

CARDIOLOGY IN THE YOUNG , vol.31, no.4, pp.568-576, 2021 (SCI-Expanded) Sustainable Development

Clinical characteristics and growth hormone treatment in patients with prader-willi syndrome

Cakir A. D., BAŞ F., Akin O., ŞIKLAR Z., Ozcabi B., BERBEROĞLU M., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.13, no.3, pp.308-319, 2021 (SCI-Expanded) Sustainable Development

The Effectiveness of Sirolimus Treatment in Two Rare Disorders with Nonketotic Hypoinsulinemic Hypoglycemia: The Role of mTOR Pathway

ŞIKLAR Z., Cetin T., ÇAKAR N., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, no.4, pp.439-443, 2020 (SCI-Expanded)

A Rare Cause of Sleep-Disordered Breathing: ROHHAD Syndrome

ÖZCAN G., ÖZSU CAVGA E., ŞIKLAR Z., Cobanoglu N.

Frontiers in Pediatrics , vol.8, 2020 (SCI-Expanded)

Intramuscular Short-term ACTH Test for the Determination of Adrenal Function in Children: Safe, Effective and Reliable

ÖZSU CAVGA E., ŞIKLAR Z., Bilici E., CERAN A., Uyanik R., Cetin T., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, no.3, pp.241-247, 2020 (SCI-Expanded)

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

Selbuz S., Kansu Tanca A., Berberoğlu M., Şıklar Z., Kuloglu Z.

EUROPEAN JOURNAL OF CLINICAL NUTRITION , vol.74, no.8, pp.1173-1180, 2020 (SCI-Expanded)

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., BAŞ F., GÜRAN T., Akberzade A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, no.2, pp.150-159, 2020 (SCI-Expanded)

Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations

Cohen E., Belkacem S., Fedala S., Collot N., Khallouf E., Dastot F., et al.

HUMAN MUTATION , vol.40, no.11, pp.2033-2043, 2019 (SCI-Expanded)

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study

Hatun S., Mutlu G. Y., Cinaz P., DEMİRCİOĞLU S., Ekberzade A., BEREKET A., et al.

DIABETIC MEDICINE , vol.36, no.10, pp.1243-1250, 2019 (SCI-Expanded) Sustainable Development

Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome

EVLİYAOĞLU S. O., Cakir A. D., BAŞ F., Akin O., ŞIKLAR Z., Ozcabi B., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.423, 2019 (SCI-Expanded)

Metabolically Unhealthy Obese Children and Adolescents Have Higher Bone Mineral Density Than Normal weighted controls but Lower than Metabolically Healthy Obeses: No Effect of FGF21 Levels

Akduman F., ŞIKLAR Z., ÖZSU CAVGA E., DOĞAN Ö., Kir M., BERBEROĞLU M.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.38-39, 2019 (SCI-Expanded)

Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis

ÖZSU CAVGA E., CERAN A., Uyanik R., Bilici E., Cetin T., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.91, pp.504-505, 2019 (SCI-Expanded)

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

EREN E., Ergur A. T., İŞGÜVEN Ş. P., Bitkin E. C., BERBEROĞLU M., ŞIKLAR Z., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.11, no.2, pp.149-156, 2019 (SCI-Expanded) Sustainable Development

Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

ABACI A., Catli G., Kirbiyik O., Sahin N. M., Abali Z. Y., Unal E., et al.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.42, no.4, pp.453-470, 2019 (SCI-Expanded)

Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?

Salman D. O., ŞIKLAR Z., Ilarslan E. N. C., ÖZÇAKAR Z. B., Kocaay P., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.11, no.1, pp.46-54, 2019 (SCI-Expanded) Sustainable Development

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia

Cetin T., ŞIKLAR Z., Kocaay P., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.4, pp.373-376, 2018 (SCI-Expanded)

Denosumab Treatment of Giant-Cell Tumors

Yavuz G., Unal E., Tacyildiz N., Dincaslan H., Tanyildiz H. G., Aksoy B. A., et al.

PEDIATRIC BLOOD & CANCER , 2018 (SCI-Expanded)

Monogenic Diabetes Not Caused By Mutations in Mody Genes: A Very Heterogenous Group of Diabetes

Şıklar Z., De Franco E., Johnson M. B., Flanagan S. E., Ellard S., Ceylaner S., et al.

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES , vol.126, no.10, pp.612-618, 2018 (SCI-Expanded) Sustainable Development

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

Camtosun E., ŞIKLAR Z., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.3, pp.247-255, 2018 (SCI-Expanded)

The Diagnostic Value of Anti-Mullerian Hormone in Early Post Menarche Adolescent Girls with Polycystic Ovarian Syndrome

Kocaay P., ŞIKLAR Z., Buyukfirat S., BERBEROĞLU M.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.31, no.4, pp.362-366, 2018 (SCI-Expanded) Sustainable Development

The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years

BERBEROĞLU M., ŞIKLAR Z.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.1, pp.30-37, 2018 (SCI-Expanded)

Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

Cetinkaya S., Poyrazoglu S., BAŞ F., Ercan O., Yildiz M., Adal E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.2, pp.175-184, 2018 (SCI-Expanded)

Syndromic Patients with Negative Islet Autoantibodies Should Be Tested for Mongenic Diabetes: Lessons from Patient with TRMT10A Mutation

ŞIKLAR Z., Colclough K., Patel K. A., Cetin T., BERBEROĞLU M.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.235, 2018 (SCI-Expanded) Sustainable Development

Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., ABACI A., BAŞ F., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.109-110, 2018 (SCI-Expanded)

Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology

Patel K. A., Colclough K., Ozbek M. N., Yildiz M., GÜRAN T., Kocyigit C., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.213, 2018 (SCI-Expanded) Sustainable Development

Contribution of Functionally Assessed GHRHR Mutations to Idiopathic Isolated Growth Hormone Deficiency in a Cohort of 312 Unrelated Patients

Cohen E., Belkacem S., Fedala S., Collot N., Khallouf E., Dastot F., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.54-55, 2018 (SCI-Expanded)

Central Precocious Puberty Appeared in Infancy Period in a Patient of Sotos Syndrome

Cetin T., Ceylaner S., ŞIKLAR Z., BERBEROĞLU M.

HORMONE RESEARCH IN PAEDIATRICS , vol.90, pp.538, 2018 (SCI-Expanded)

Plasma Amino-Terminal Propeptide of C-Type Natriuretic Peptide Concentration in Normal-Weight and Obese Children

TOPÇU S., ÖZHAN B., ALKAN A., AKYOL M., ORHON F., BAŞKAN S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.4, pp.308-314, 2017 (SCI-Expanded) Sustainable Development

Childhood Sustained Hypercalcemia: A Diagnostic Challenge

Ilarslan N. E. C., ŞIKLAR Z., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.4, pp.315-322, 2017 (SCI-Expanded)

Multiple Presentations of LRBA Deficiency: a Single-Center Experience

Bal S. K., Haskologlu S., Serwas N. K., Islamoglu C., Aytekin C., Kendirli T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , no.8, pp.790-800, 2017 (SCI-Expanded)

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

Johnson M. B., De Franco E., Allen H. L., Al Senani A., Elbarbary N., ŞIKLAR Z., et al.

DIABETES , vol.66, no.8, pp.2316-2322, 2017 (SCI-Expanded)

Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height

Savas-Erdeve S., Cetinkaya S., Abali Z. Y., Poyrazoglu S., BAŞ F., BERBEROĞLU M., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.30, no.7, pp.759-766, 2017 (SCI-Expanded)

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

Camtosun E., ŞIKLAR Z., Ceylaner S., Kocaay P., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.2, pp.163-167, 2017 (SCI-Expanded)

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

Yekeduz M. K., Şıklar Z., Burgu B., Kuloğlu Z., Kocaay P., Camtosun E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.9, no.2, pp.168-171, 2017 (SCI-Expanded)

PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY

ABACI A., ÇATLI G., Kirbiyik O., Sahin N. M., Abali Z. Y., Unal E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.551-552, 2017 (SCI-Expanded)

CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY

EREN E., Ergur A. T., İŞGÜVEN Ş. P., Bitkin E. C., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.313-314, 2017 (SCI-Expanded) Sustainable Development

Acute reversible cardiomyopathy and heart failure in a child with acute adrenal crisis

Odek C., KENDİRLİ T., Kocaay P., Azapagasi E., UÇAR T., ŞIKLAR Z., et al.

PAEDIATRICS AND INTERNATIONAL CHILD HEALTH , vol.37, no.2, pp.148-151, 2017 (SCI-Expanded)

THE EFFECTIVENESS IF SIROLIMUS TREATMENT IN TWO RARE DISORDERS WITH NONKETOTIC HYPOINSULINEMIC HYPOGLYCEMIA

ŞIKLAR Z., Cetin T., Kacar N., BERBEROĞLU M.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.173, 2017 (SCI-Expanded)

THE EVALUATION OF CASES WITH GONADAL DYSGENESIS: CLINICAL EXPERIENCE FOR 18 YEARS

BERBEROĞLU M., ŞIKLAR Z.

HORMONE RESEARCH IN PAEDIATRICS , vol.88, pp.553-554, 2017 (SCI-Expanded)

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

ŞIKLAR Z., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.4, pp.375-380, 2016 (SCI-Expanded)

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

ŞIKLAR Z., Karatas D., DOĞU E. F., Hacihamdioglu B., İKİNCİOĞULLARI K. A., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.3, pp.276-281, 2016 (SCI-Expanded)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

ŞIKLAR Z., Genens M., Poyrazoglu S., BAŞ F., Darendeliler F., Bundak R., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.3, pp.305-312, 2016 (SCI-Expanded)

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Taylan F., Costantini A., Coles N., Pekkinen M., Heon E., ŞIKLAR Z., et al.

JOURNAL OF BONE AND MINERAL RESEARCH , vol.31, no.8, pp.1577-1585, 2016 (SCI-Expanded)

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

Delil K., KARABULUT H. G., Hacihamdioglu B., ŞIKLAR Z., BERBEROĞLU M., Ocal G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, pp.144-149, 2016 (SCI-Expanded)

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Savas-Erdeve S., ŞIKLAR Z., Hacihamdioglu B., Kocaay P., Camtosun E., Ocal G., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.8, no.2, pp.211-217, 2016 (SCI-Expanded)

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study

Atay Z., Yesilkaya E., Erdeve S. S., DEMİRCİOĞLU S., Akin L., EREN E., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , vol.101, no.5, pp.1980-1988, 2016 (SCI-Expanded)

Non-Mody Monogenic Diabetes: A Very Heterogenous and Problematic Group of Diabetes

ŞIKLAR Z., De Franco E., FlanagaN S., Ellard S., Ceylaner S., Boztug K., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.99-100, 2016 (SCI-Expanded) Sustainable Development

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

Kocaay P., ŞIKLAR Z., Ellard S., Yagmurlu A., Camtosun E., Erden E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.85, no.6, pp.421-425, 2016 (SCI-Expanded)

The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels

ŞIKLAR Z., Kocaay P., Camtosun E., Isakoca M., Hacihamdioglu B., Erdeve S. S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.4, pp.301-306, 2015 (SCI-Expanded)

Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development

Topcu V., ILGIN RUHİ H., ŞIKLAR Z., KARABULUT H. G., BERBEROĞLU M., Hacihamdioglu B., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.28, no.11-12, pp.1257-1263, 2015 (SCI-Expanded)

Intrathyroidal Ectopic Thymus in Children Retrospective Analysis of Grayscale and Doppler Sonographic Features

Yildiz A. E., CEYHAN K., ŞIKLAR Z., BİLİR P., YAĞMURLU E. A., BERBEROĞLU M., et al.

JOURNAL OF ULTRASOUND IN MEDICINE , vol.34, no.9, pp.1651-1656, 2015 (SCI-Expanded)

MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation

Garg N., Bademci G., Foster J., ŞIKLAR Z., BERBEROĞLU M., Tekin M.

JOURNAL OF PEDIATRICS , vol.167, no.2, pp.489-491, 2015 (SCI-Expanded)

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

BAŞ F., Uyguner Z. O., Darendeliler F., AYCAN Z., Cetinkaya E., BERBEROĞLU M., et al.

ENDOCRINE , vol.49, no.2, pp.479-491, 2015 (SCI-Expanded)

A Deep Intronic HADH Splicing Mutation (c.636+471G > T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

Camtosun E., Flanagan S. E., Ellard S., ŞIKLAR Z., Hussain K., Kocaay P., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.2, pp.144-147, 2015 (SCI-Expanded)

Diagnostic Characteristics and Metabolic Risk Factors of Cases with Polycystic Ovary Syndrome during Adolescence

ŞIKLAR Z., BERBEROĞLU M., Camtosun E., Kocaay P.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.28, no.2, pp.78-83, 2015 (SCI-Expanded)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

Poyrazoglu S., Akcay T., ARSLANOĞLU İ., ATABEK M. E., Atay Z., BERBEROĞLU M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.7, no.1, pp.37-44, 2015 (SCI-Expanded) Sustainable Development

Three cases of Wolfram syndrome with different clinical aspects

Camtosun E., ŞIKLAR Z., Kocaay P., Ceylaner S., Flanagan S. E., Ellard S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.28, no.3-4, pp.433-438, 2015 (SCI-Expanded)

Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification

Ocal G., BERBEROĞLU M., ŞIKLAR Z., AYCAN Z., Hacihamdioglu B., Erdeve S. S., et al.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.28, no.1, pp.6-11, 2015 (SCI-Expanded)

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

Kocaay P., ŞIKLAR Z., Camtosun E., KENDİRLİ T., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.4, pp.254-257, 2014 (SCI-Expanded) Sustainable Development

ARE THYROID CANCERS INCREASING IN YOUNG ADOLESCENTS

Cabi E. U., Tacyildiz N., Yavuz G., Dincaslan H., Tanyildiz G., Berberoglu M., et al.

PEDIATRIC BLOOD & CANCER , 2014 (SCI-Expanded)

DENOSUMAB TREATMENT OF GIANT-CELL TUMOR OF MAXILLA IN A 9-YEAR-OLD GIRL

Yavuz G., Cabi E. U., Tacyildiz N., Dincaslan H., Pekpak E., Aksoy B., et al.

PEDIATRIC BLOOD & CANCER , 2014 (SCI-Expanded)

Gastric carcinoid tumor in a 14-year old girl

TUNA KIRSAÇLIOĞLU C., KULOĞLU Z., KANSU TANCA A., ENSARİ A., ŞIKLAR Z., BERBEROĞLU M., et al.

SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY , vol.49, no.11, pp.1391-1393, 2014 (SCI-Expanded)

The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

Hacihamdioglu B., Ocal G., BERBEROĞLU M., Erdeve S. S., Camtosun E., Kocaay P., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, no.9-10, pp.901-908, 2014 (SCI-Expanded) Sustainable Development

PREPERITONEAL FAT TISSUE MAY BE ASSOCIATED WITH ARTERIAL STIFFNESS IN OBESE ADOLESCENTS

Hacihamdioglu B., Ocal G., BERBEROĞLU M., ŞIKLAR Z., FİTOZ Ö. S., Tutar E., et al.

ULTRASOUND IN MEDICINE AND BIOLOGY , vol.40, no.5, pp.871-876, 2014 (SCI-Expanded)

A Novel Heterozygous Mutation in Steroidogenic Factor-1 in Pubertal Virilization of a 46,XY Female Adolescent

ŞIKLAR Z., BERBEROĞLU M., Ceylaner S., Camtosun E., Kocaay P., GÖLLÜ BAHADIR G., et al.

JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY , vol.27, no.2, pp.98-101, 2014 (SCI-Expanded)

A NOVEL MUTATION IN THE CALCIUM SENSING RECEPTOR GENE IN A NEONATE WITH SEVERE HYPERPARATHYROIDISM

Kahvecioglu D., Atasay B., BERBEROĞLU M., Yildiz D., Cakir U., Akduman H., et al.

GENETIC COUNSELING , vol.25, no.3, pp.331-335, 2014 (SCI-Expanded)

Syndromic Disorders with Short Stature

ŞIKLAR Z., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.6, no.1, pp.1-8, 2014 (SCI-Expanded)

ADHERENCE TO GROWTH HORMONE THERAPY: RESULTS OF A MULTICENTER STUDY

Aydin B. K., AYCAN Z., ŞIKLAR Z., BERBEROĞLU M., Ocal G., Cetinkaya S., et al.

ENDOCRINE PRACTICE , vol.20, no.1, pp.46-51, 2014 (SCI-Expanded)

THYROID CANCERS IN YOUNG ADOLESCENTS AT A UNIVERSITY HOSPITAL

Cabi E. U., Tacyildiz N., Yavuz G., Tanyildiz G., Dincaslan H., Ocal G., et al.

PEDIATRIC BLOOD & CANCER , pp.103, 2013 (SCI-Expanded)

Pathophysiology of critical illness hyperglycemia in children

Hacihamdioglu B., KENDİRLİ T., Ocal G., ŞIKLAR Z., Erdeve S. S., Ince E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.26, no.7-8, pp.715-720, 2013 (SCI-Expanded)

Late neonatal hypocalcemic tetany as a manifestation of unrecognized maternal primary hyperparathyroidism

Cakir U., Alan S., ERDEVE Ö., Atasay B., ŞIKLAR Z., BERBEROĞLU M., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.55, no.4, pp.438-440, 2013 (SCI-Expanded)

Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation

Flanagan S. E., Xie W., Caswell R., Damhuis A., Vianey-Saban C., Akcay T., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.92, no.1, pp.131-136, 2013 (SCI-Expanded)

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

Simsek D. G., AYCAN Z., ÖZEN S., Cetinkaya S., Kara C., ABALI S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.5, no.1, pp.20-26, 2013 (SCI-Expanded) Sustainable Development

Rare childhood tumors in a Turkish pediatric oncology center

TAÇYILDIZ N., Özyörük D., Yavuz G., Ünal E. C., DİNÇASLAN H., Tanyildiz G. O., et al.

Indian Journal of Medical and Paediatric Oncology , vol.34, no.4, pp.264-269, 2013 (SCI-Expanded) Sustainable Development

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?

Ocal G., BERBEROĞLU M., ŞIKLAR Z., ILGIN RUHİ H., Tukun A., Camtosun E., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.171, no.10, pp.1497-1502, 2012 (SCI-Expanded)

Hashimoto Encephalopathy Causing Drug-Resistant Status Epilepticus Treated With Plasmapheresis

BEKTAŞ Ö., Yilmaz A., KENDİRLİ T., ŞIKLAR Z., Deda G.

PEDIATRIC NEUROLOGY , vol.46, no.2, pp.132-135, 2012 (SCI-Expanded)

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

GÜRBÜZ F., KOTAN L. D., Mengen E., ŞIKLAR Z., BERBEROĞLU M., Dokmetas S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.3, pp.121-126, 2012 (SCI-Expanded)

Relationships Between Osteocalcin, Glucose Metabolism, and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?

Abseyi N., ŞIKLAR Z., BERBEROĞLU M., Hacihamdioglu B., Erdeve S. S., Ocal G.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.4, no.4, pp.182-188, 2012 (SCI-Expanded) Sustainable Development

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

BAŞ F., Darendeliler F., AYCAN Z., Cetinkaya E., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.77, no.2, pp.85-93, 2012 (SCI-Expanded)

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

ŞIKLAR Z., BERBEROĞLU M., Yagmurlu A., Hacihamdioglu B., Erdeve S. S., FİTOZ Ö. S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , no.1, pp.30-33, 2012 (SCI-Expanded)

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

ŞIKLAR Z., Ellard S., OKULU E., BERBEROĞLU M., Young E., Erdeve S. S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.11-12, pp.1077-1080, 2011 (SCI-Expanded) Sustainable Development

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche

Erdeve S. S., BERBEROĞLU M., KUTLAY N., ŞIKLAR Z., Hacihamdioglu B., Tukun A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.11-12, pp.965-970, 2011 (SCI-Expanded)

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

Ocal G., Flanagan S. E., Hacihamdioglu B., BERBEROĞLU M., ŞIKLAR Z., Ellard S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.11-12, pp.1019-1023, 2011 (SCI-Expanded) Sustainable Development

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

ŞIKLAR Z., Ocal G., BERBEROĞLU M., Hacihamdioglu B., Erdeve S. S., Egin Y., et al.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , vol.17, no.6, pp.585-589, 2011 (SCI-Expanded) Sustainable Development

Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation

Savas-Erdeve S., BERBEROĞLU M., ŞIKLAR Z., Hacihamdioglu B., Ocal G., ERTEM M., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.9-10, pp.853-855, 2011 (SCI-Expanded)

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis

Savas-Erdeve S., BERBEROĞLU M., Oygar P., ŞIKLAR Z., KENDİRLİ T., Hacihamdioglu B., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.3, no.3, pp.149-153, 2011 (SCI-Expanded) Sustainable Development

Case Report: Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties

Hacihamdioglu B., BERBEROĞLU M., ŞIKLAR Z., DOĞU E. F., BİLİR P., Erdeve S. S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.3, no.2, pp.95-97, 2011 (SCI-Expanded)

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis

Ergur A. T., EVLİYAOĞLU S. O., ŞIKLAR Z., BİLİR P., Ocal G., BERBEROĞLU M.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.3, no.1, pp.18-21, 2011 (SCI-Expanded)

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

ŞIKLAR Z., BERBEROĞLU M., Erdeve S. S., Hacihamdioglu B., Ocal G., Egin Y., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.1-2, pp.21-24, 2011 (SCI-Expanded) Sustainable Development

Breast disorders in adolescents Ergenlerde görülen meme hastalıkları

ŞIKLAR Z.

Turk Pediatri Arsivi , vol.46, no.SUPPL.1, pp.84-87, 2011 (SCI-Expanded)

The endocrine spectrum of intracranial cysts in childhood and review of the literature

Erdeve S. S., Ocal G., BERBEROĞLU M., ŞIKLAR Z., Hacihamdioglu B., EVLİYAOĞLU S. O., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.24, no.11-12, pp.867-875, 2011 (SCI-Expanded) Sustainable Development

Is Adrenocorticotropic Hormone Deficiency Really Rare in Patients with Idiopathic Growth Hormone Deficiency and Normal Thyroid Function Tests?

Erdeve S. S., Ocal G., BERBEROĞLU M., ŞIKLAR Z., Hacihamdioglu B.

HORMONE RESEARCH IN PAEDIATRICS , vol.75, no.3, pp.200-205, 2011 (SCI-Expanded)

Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: Successful treatment with growth hormone despite late admission and severe growth retardation

ŞIKLAR Z., BERBEROĞLU M., Legendre M., Amselem S., EVLİYAOĞLU S. O., Hacihamdioǧlu B., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.2, no.4, pp.164-167, 2010 (SCI-Expanded)

Celiac disease and autoimmune thyroid disease in children with type 1 diabetes mellitus: Clinical and HLA-genotyping Results

Ergür A. T., Öçal G., BERBEROĞLU M., Adiyaman P., ŞIKLAR Z., Aycan Z., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.2, no.4, pp.151-154, 2010 (SCI-Expanded) Sustainable Development

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

Ocal G., BERBEROĞLU M., ŞIKLAR Z., Bilir P., Uslu R., Yagmurlu A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.23, no.11, pp.1123-1132, 2010 (SCI-Expanded)

A novel mutation of 5 alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

Erdeve S. S., AYCAN Z., BERBEROĞLU M., ŞIKLAR Z., Hacihamdioglu B., Sipahi K., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.169, no.8, pp.991-995, 2010 (SCI-Expanded)

The effect of colchicine on physical growth in children wA +/- th familial mediterranean fever

ÖZÇAKAR Z. B., Kadioglu G., ŞIKLAR Z., Kavaz A., Aksanal F. N., BERBEROĞLU M., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.169, no.7, pp.825-828, 2010 (SCI-Expanded)

Genoa syndrome and central diabetes insipidus: A case report

Hacihamdioǧlu B., ŞIKLAR Z., Erdeve Ş. S., BERBEROĞLU M., Deda G., Tiraş S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.2, no.2, pp.89-91, 2010 (SCI-Expanded) Sustainable Development

Long-term follow-up of a pseudohypoparathyroidism type 1a patient with missense mutation (pro115ser) in exon 5

Erdeve Ş. S., BERBEROĞLU M., ŞIKLAR Z., EVLİYAOĞLU S. O., Hiort O., Öcal G.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.2, no.2, pp.85-88, 2010 (SCI-Expanded)

Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake

Hacihamdioglu B., BERBEROĞLU M., ŞIKLAR Z., Erdeve S. S., Ocal G., Tutar E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.23, no.4, pp.363-368, 2010 (SCI-Expanded)

Vitamin D deficiency in Turkish mothers and their neonates and in women of reproductive age

Ergür A. T., BERBEROĞLU M., Atasay B., ŞIKLAR Z., BİLİR P., ARSAN S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.1, no.6, pp.266-269, 2009 (SCI-Expanded) Sustainable Development

Evaluation of Final Height and Parentally Adjusted Height Deficit in Isolated Growth Hormone Deficient Children With or Without Short Parents

ŞIKLAR Z., BERBEROĞLU M., Ocal G., BİLİR P., Erdeve S. S.

ENDOCRINOLOGIST , vol.19, no.6, pp.285-287, 2009 (SCI-Expanded)

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Coker A., Cetinkaya E., Dundar B., ŞIKLAR Z., Buyukgebiz A., ARMAN A.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.22, no.10, pp.937-946, 2009 (SCI-Expanded)

Treatment of autonomous ovarian follicular cyst with long-term anastrozole therapy

Engiz O., BERBEROĞLU M., ŞIKLAR Z., BİLİR P., Ocal G.

INDIAN JOURNAL OF PEDIATRICS , vol.76, no.9, pp.950-951, 2009 (SCI-Expanded)

Combined evaluation of IGF-1 and IGFBP-3 as an index of efficacy and safety in growth hormone treated patients

ŞIKLAR Z., Öcal G., BERBEROĞLU M., BİLİR P.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.1, no.5, pp.240-243, 2009 (SCI-Expanded)

Early prophylactic thyroidectomy for RETmutation-positive MEN 2B

Engiz O., Ocal G., ŞIKLAR Z., Erdogan M., KOLOĞLU M., Percinel S., et al.

PEDIATRICS INTERNATIONAL , vol.51, no.4, pp.590-593, 2009 (SCI-Expanded)

"Maternal/Neonatal" Iodine Status in Patients with Prolonged Physiological Jaundice

ŞIKLAR Z., Ocal G., Bilir P., Ergur A., BERBEROĞLU M.

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES , vol.117, no.7, pp.312-315, 2009 (SCI-Expanded)

Gender Dysphoria and Gender Change in an Adolescent with 45,X/46,XY Mixed Gonadal Dysigenesis

Oecal G., BERBEROĞLU M., ŞIKLAR Z., Bilir P.

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES , vol.117, no.6, pp.301-304, 2009 (SCI-Expanded)

Early and severe presentation of vitamin D deficiency and nutritional rickets among hospitalized infants and the effective factors

Tezer H., ŞIKLAR Z., Dallar Y., Dogankoc S.

TURKISH JOURNAL OF PEDIATRICS , vol.51, no.2, pp.110-115, 2009 (SCI-Expanded) Sustainable Development

Cytokines as a Common Components of Two Different Disorders: Metabolic Syndrome and Hemophagocytic Lymphohystiositosis

Silklar Z., BERBEROĞLU M., Uysal Z., Citak F. E., Bilir P., Ertem M., et al.

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES , vol.117, no.2, pp.57-59, 2009 (SCI-Expanded)

A novel mutation in 5 alpha-steroid reductase 2 deficiency (CD 65 pro-ALA) in a Turkish family

Ocal G., Erdeve S. S., BERBEROĞLU M., ŞIKLAR Z., Hacihamdioglu B., Sipahi K., et al.

HORMONE RESEARCH , vol.72, pp.367, 2009 (SCI-Expanded)

The exon 3 deleted/full length growth hormone receptor polymorphism and response to GH therapy in GH deficiency and Turner syndrome: a multicenter study

Darendeliler F. F., BAŞ F., Bozkurt N., Uzunhan O., AYCAN Z., Cetinkaya E., et al.

HORMONE RESEARCH , vol.72, pp.109, 2009 (SCI-Expanded)

Risk Factors for Non-Alcoholic Fatty Liver Disease in Obese Children

Engiz O., BERBEROĞLU M., ŞIKLAR Z., Ocal G.

HORMONE RESEARCH , vol.72, no.1, pp.63-64, 2009 (SCI-Expanded)

Contribution of clinic, metabolic, and genetic factors on hypertension in obese children and adolescents

ŞIKLAR Z., BERBEROĞLU M., Erdeve S. S., Hacihamdioglu B., Ocal G., Egin Y., et al.

HORMONE RESEARCH , vol.72, pp.411, 2009 (SCI-Expanded)

The relationship between IGF-1 response and 1st year height velocity on two different doses of GH in idiopathic GH deficiency (IGHD): a randomized, prospective clinical study

Bundak R., Arslanoglu I., Berberoglu M., ŞIKLAR Z., Isguven P., Ocal G., et al.

HORMONE RESEARCH , vol.72, pp.104-105, 2009 (SCI-Expanded)

Molecular analysis of PIT1, PROP1, LHX3, and HESX1 in patients with combined pituitary hormone deficiency: multicenter study

BAŞ F., Darendeliler F. F., Oyguner O., AYCAN Z., Cetinkaya E., BERBEROĞLU M., et al.

HORMONE RESEARCH , vol.72, pp.396-397, 2009 (SCI-Expanded)

What is the Bogy mass index threshold value for children that metabolic syndrome develops?

Pekacar T., BİLİR P., ŞIKLAR Z., Hacihamdioglu B., Erdeve S. S.

HORMONE RESEARCH , vol.72, pp.141, 2009 (SCI-Expanded)

Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients

ŞIKLAR Z., Çitak F. E., Uysal Z., Öçal G., ERTEM M., Engiz Ö., et al.

Pediatric Hematology and Oncology , vol.25, no.7, pp.630-637, 2008 (SCI-Expanded) Sustainable Development

Celiac disease associated with nephrotic syndrome

Gurkas E., ÖZÇAKAR Z. B., Kuloglu Z., ŞIKLAR Z., Kahraman I., Kazanci G., et al.

PEDIATRIC NEPHROLOGY , vol.23, no.9, pp.1642, 2008 (SCI-Expanded)

Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey

Sadeghi F., KUTLAY N., BERBEROĞLU M., Cetinkaya E., AYCAN Z., Kara C., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.8, pp.781-787, 2008 (SCI-Expanded)

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome

Erur A. T., Ocal G., BERBEROĞLU M., Tekin M., KILIÇ B. G., AYCAN Z., et al.

PEDIATRICS INTERNATIONAL , vol.50, no.2, pp.172-174, 2008 (SCI-Expanded)

Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up

Kara C., Ocal G., BERBEROĞLU M., ŞIKLAR Z., Adiyaman P.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.21, no.3, pp.251-256, 2008 (SCI-Expanded)

Hypophosphatasia associated with pseudotumor cerebri and respiratory insufficiency

TEBER S., Sezer T., Kafali M., KENDİRLİ T., ŞIKLAR Z., BERBEROĞLU M., et al.

INDIAN JOURNAL OF PEDIATRICS , vol.75, no.2, pp.186-188, 2008 (SCI-Expanded)

Life quality in girls with Turner syndrome a cross sectional study

BİDECİ A., EVLİYAOĞLU S. O., Cetinkaya E., AYCAN Z., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH , vol.70, pp.178, 2008 (SCI-Expanded)

Heterozygous Q318X mutation of 21 Hydroxylase gene in a neonate with scrotal pigmentation and mildly elevated 17OHP level

ŞIKLAR Z., BERBEROĞLU M., Tukun A., Ocal G.

HORMONE RESEARCH , vol.70, pp.252, 2008 (SCI-Expanded)

Risk factors for hepatic steatosis in Turkish children (Predictors of non-alcoholic fatty liver disease in obese Turkish children)

Engiz O., BERBEROĞLU M., ŞIKLAR Z., BİLİR P., Ocal G.

HORMONE RESEARCH , vol.70, pp.255, 2008 (SCI-Expanded)

Evaluation of permanent growth hormone deficiency (GHD) in young adults with childhood onset GHD: A multicenter study

BERBEROĞLU M., ŞIKLAR Z., Darendeliler F., Poyrazoglu S., DARCAN Ş., Isguven P., et al.

HORMONE RESEARCH , vol.70, pp.103, 2008 (SCI-Expanded)

Characterization of GH-N mutations in children with isolated growth hormone deficiency in Turkish population

Arman A., Cetinkaya E., Dundar B., ŞIKLAR Z., Coker A., Buyukgebiz A.

HORMONE RESEARCH , vol.70, pp.197, 2008 (SCI-Expanded)

Diagnostic value of contrast-enhanced MR angiography in a child with MIBG-negative recurrent pheochromocytoma

ŞIKLAR Z., Oecal G., BERBEROĞLU M., Adiyamam P., Erguer A., Cetinkaya E., et al.

ENDOCRINOLOGIST , vol.18, no.1, pp.19-22, 2008 (SCI-Expanded)

Hypocalcemic seizure due to congenital rickets in the first day of life

Erdeve Ö., Atasay B., Arsan S., ŞIKLAR Z., Oecal G., BERBEROĞLU M.

TURKISH JOURNAL OF PEDIATRICS , vol.49, no.3, pp.301-303, 2007 (SCI-Expanded)

Functional ovarian hyperandrogenism and polycystic ovary syndrome in prepubertal girls with obesity and/or premature pubarche

ŞIKLAR Z., Ocal G., Adiyaman P., Ergur A., BERBEROĞLU M.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.20, no.4, pp.475-481, 2007 (SCI-Expanded) Sustainable Development

Disorders of gonadal development: A broad clinical, cytogenetic and histopathologic spectrum

ŞIKLAR Z., BERBEROĞLU M., Adiyaman P., Salih M., Tükün A., Çetinkaya E., et al.

Pediatric Endocrinology Reviews , vol.4, no.3, pp.210-217, 2007 (SCI-Expanded)

Importance of thyroglobulin levels for diagnosis and monitoring of follicular thyroid carcinoma in an adolescent with severe iodine deficiency

ŞIKLAR Z., Ocal G., BERBEROĞLU M., Adiyaman P., Ergur A. T., EVLİYAOĞLU S. O., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.9, pp.1175-1178, 2006 (SCI-Expanded) Sustainable Development

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

BERBEROĞLU M., EVLİYAOĞLU S. O., Adiyaman P., Ocal G., ULUKOL B., Simsek F., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.5, pp.741-748, 2006 (SCI-Expanded)

Incidence of iodine deficiency in patients presenting with goitre - Discrepancy between clinical and ultrasonographic evaluation of the thyroid: Comparison of patients with and without autoimmune thyroiditis - Clinical, hormonal and urinary iodine excretion studies

EVLİYAOĞLU S. O., BERBEROĞLU M., Adiyaman P., AYCAN Z., Ergur A., ŞIKLAR Z., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.1, pp.39-44, 2006 (SCI-Expanded)

Maternal/neonatal iodine status and neonatal borderline hypothyroidism

ŞIKLAR Z., Ocal G., Adiyaman P., Ergur A., Berberoglu M.

HORMONE RESEARCH , vol.65, pp.48-49, 2006 (SCI-Expanded)

Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients

ŞIKLAR Z., Citak F. E., Uysal Z., Ocal G., Ertem M., Engiz O., et al.

HORMONE RESEARCH , vol.65, pp.65, 2006 (SCI-Expanded)

Diurnal variation of height in children

ŞIKLAR Z., Sanli E., Dallar Y., Tanyer G.

PEDIATRICS INTERNATIONAL , vol.47, no.6, pp.645-648, 2005 (SCI-Expanded)

Response to growth hormone with respect to pubertal status on increased dose in idiopathic growth hormone deficiency: An analysis of Turkish children in the KIGS database (Pfizer International Growth Study)

Darendeliler F., BERBEROĞLU M., Ocal G., Adiyaman P., Bundak R., Gunoz H., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.18, no.10, pp.949-954, 2005 (SCI-Expanded)

Superoxide dismutase activity and zinc and copper concentrations in growth retardation

Kocaturk P., Kavas G., Erdeve Ö., ŞIKLAR Z.

BIOLOGICAL TRACE ELEMENT RESEARCH , vol.102, no.1-3, pp.51-59, 2004 (SCI-Expanded)

Is hypertriglyceridaemia a new concept for visceral leishmaniasis?

Erdeve Ö., Dallar Y., ŞIKLAR Z.

ANNALS OF TROPICAL PAEDIATRICS , vol.24, no.4, pp.369, 2004 (SCI-Expanded)

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and celiac disease

AYCAN Z., BERBEROĞLU M., Adiyaman P., Ergur A., ENSARİ A., EVLİYAOĞLU S. O., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.17, no.11, pp.1565-1569, 2004 (SCI-Expanded) Sustainable Development

An infantile Cushing syndrome due to misuse of topical steroid

ŞIKLAR Z., Bostanci I., Atli O., Dallar Y.

PEDIATRIC DERMATOLOGY , vol.21, no.5, pp.561-563, 2004 (SCI-Expanded)

Antioxidant superoxide dismutase activity in obese children

Erdeve Ö., ŞIKLAR Z., Kocaturk P., Dallar Y., Kavas G.

BIOLOGICAL TRACE ELEMENT RESEARCH , vol.98, no.3, pp.219-227, 2004 (SCI-Expanded)

Zinc deficiency: a contributing factor of short stature in growth hormone deficient children

ŞIKLAR Z., Tuna C., Dallar Y., Tanyer G.

JOURNAL OF TROPICAL PEDIATRICS , vol.49, no.3, pp.187-188, 2003 (SCI-Expanded)

Zinc treatment affects superoxide dismutase activity in growth retardation

Kocaturk P., ŞIKLAR Z., Kavas G., Dallar Y., Tanyer G.

BIOLOGICAL TRACE ELEMENT RESEARCH , vol.90, no.1-3, pp.39-46, 2002 (SCI-Expanded)

Borderline congenital hypothyroidism in the neonatal period

ŞIKLAR Z., Tezer H., Dallar Y., Tanyer G.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.15, no.6, pp.817-821, 2002 (SCI-Expanded)

Multiple dose IVIG treatment in neonatal immune hemolytic jaundice

Tanyer G., ŞIKLAR Z., Dallar Y., Yildirmak Y., Tiras U.

JOURNAL OF TROPICAL PEDIATRICS , vol.47, no.1, pp.50-53, 2001 (SCI-Expanded)

Pica and intoxication in childhood

ŞIKLAR Z., Tanyer G., Dallar Y., Gunay S.

CLINICAL PEDIATRICS , vol.39, no.10, pp.624-625, 2000 (SCI-Expanded)

Hajdu-Cheney syndrome with growth hormone deficiency and neuropathy

ŞIKLAR Z., Tanyer G., Dallar Y., Aksoy F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.13, no.7, pp.951-954, 2000 (SCI-Expanded)

Articles Published in Other Journals

Evaluation of the Nutritional Status and Eating Behaviors of Young Children with Type 1 Diabetes and Healthy Peers: A Controlled Cross Sectional Study

ÖNAL S., UÇAR A., ŞIKLAR Z., BERBEROĞLU M.

Türkiye Diyabet ve Obezite Dergisi , vol.1, pp.51-58, 2024 (Peer-Reviewed Journal)

Approach to Rickets: Is It Calciopenic or Phosphopenic?

Abseyi S. N., ŞIKLAR Z.

Turkish Archives of Pediatrics , vol.58, no.5, pp.458-466, 2023 (ESCI)

Impact of the COVID-19 pandemic on diabetic ketoacidosis management in the pediatric intensive care unit

KAHVECİ F., Ocak B. Ö., GÜN E., Gurbanov A., Uçmak H., Aslan A. D., et al.

Acute and Critical Care , vol.38, no.3, pp.371-379, 2023 (ESCI)

Clinical Characteristics and Treatment Outcomes of Children with Primary Osteoporosis

ÇETİN S. K., ŞIKLAR Z., AYCAN Z., OZSU E., CERAN A., ŞENYAZAR G., et al.

Turkish archives of pediatrics (Online) , vol.58, no.3, pp.314-321, 2023 (Scopus)

Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A Single-Center Experience

Çetin S., ŞIKLAR Z., AYCAN Z., ÖZSU E., CERAN A., Karaca S. E., et al.

Turkish Archives of Pediatrics , vol.58, no.1, pp.56-61, 2023 (ESCI)

How does an additional insulin dose for a high-fat, high-protein breakfast affect glysemic response in adolescents with type 1 diabetes?

BAYINDIR GÜMÜŞ A., KESER A., ŞIKLAR Z., BERBEROĞLU M.

MARMARA MEDICAL JOURNAL , vol.36, no.2, pp.242-248, 2023 (Scopus)

Hypophyseal Dysfunction and Difficulties in Management of Pediatric Intracranial Germ Cell Tumors

Isakoca M., Kahilogullari G., Siklar Z., Kontbay T., Unal E., Tacyildiz N., et al.

TURKISH ARCHIVES OF PEDIATRICS , vol.57, no.3, pp.362-364, 2022 (ESCI)

Investigation of early puberty prevalence and time of addition thelarche to pubarche in girls with premature pubarche: two-year follow-up results

Olgun E. G., Cetin S. K., ŞIKLAR Z., AYCAN Z., ÖZSU CAVGA E., CERAN A., et al.

CLINICAL PEDIATRIC ENDOCRINOLOGY , vol.31, no.1, pp.25-32, 2022 (ESCI)

The Relationship Between Diet Quality of Adolescents with Type 1 Diabetes and Nutritional Status and Biochemical Parameters

ŞAHİN BODUR G., KESER A., ŞIKLAR Z., BERBEROĞLU M.

ERCIYES MEDICAL JOURNAL , vol.43, no.5, pp.458-464, 2021 (ESCI)

A CROSS-SECTIONAL STUDY ON FACTORS AFFECTING DIETARY QUALITY OF ADOLESCENTS WITH TYPE 1 DIABETES

ŞAHİN BODUR G., KESER A., ŞIKLAR Z., BERBEROĞLU M.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.84, no.4, pp.552-558, 2021 (ESCI)

Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up

Cetin S., ŞIKLAR Z., ÖZSU CAVGA E., AYCAN Z., Uyanik R., Bilici M. E., et al.

CLINICAL PEDIATRIC ENDOCRINOLOGY , vol.29, no.4, pp.195-199, 2020 (ESCI)

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

Flanagan S. E., Banerjee I., Senniappan S., Laver T. W., Caswell R., Zenker M., et al.

Wellcome Open Research , vol.4, 2020 (Scopus) Sustainable Development

Treatment management with 18F-Fluoro-L-DOPA PET/CT imaging of focal congenital hyperinsulinemic hypoglycemia case Fokal Konjenital Hiperinsülinemik Hipoglisemi Olgusunda 18F-Fluoro-L-DOPA PET/BT Görüntülemesi ile Tedavi Yönetimi

KIZILCAN ÇETİN S., ŞIKLAR Z., SOYDAL Ç., Özsu E., AYCAN Z., Yağmurlu A., et al.

Turkiye Klinikleri Pediatri , vol.29, no.3, pp.187-194, 2020 (Scopus)

Esnek İnsülin Tedavisi Alan Tip 1 Diyabetli Çocuk ve Adolesanların 2 Yıllık İzlem Sonuçları ve Tedaviye Uyumun Değerlendirilmesi

ÇELİK P., ŞIKLAR Z., BERBEROĞLU M.

Türkiye Çocuk Hastalıkları Dergisi , pp.1-9, 2020 (Peer-Reviewed Journal) Sustainable Development

Neonatal effects of thyroid diseases in pregnancy and approach to the infant with increased TSH: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

ÖZÖN Z. A., Tekin N., ŞIKLAR Z., Gulcan H., Kara C., TAŞTEKİN A., et al.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, 2018 (ESCI)

Alacrima-Achalasia: Look for adrenal insufficiency: Case report

Eldem I., Bozdemir Kocaay P., ŞIKLAR Z., KULOĞLU Z., Baş Z., Uçakhan Ö. Ö., et al.

Turkiye Klinikleri Pediatri , vol.25, no.2, pp.119-123, 2016 (Scopus)

Alakrima-Akalazya: Adrenal Yetmezlik Açısından İzlem

Eldem İ., Bozdemir Kocaay P., ŞIKLAR Z., KULOĞLU Z., Uçakhan Ö. Ö., BAŞ Z., et al.

Türkiye Klinikleri Pediatri Dergisi. , vol.25, no.2, pp.119-123, 2016 (Peer-Reviewed Journal)

Is subclinical hypothyroidism increasing exogen obesity in children?

TUNA KIRSAÇLIOĞLU C., dallar y., ŞIKLAR Z.

Journal of Contemporary Medicine , vol.5, no.1, pp.1-7, 2015 (Peer-Reviewed Journal)

Pediatric hormonal disturbances after hematopoietic stem cell transplantation

ŞIKLAR Z., BERBEROĞLU M.

Expert Review of Endocrinology and Metabolism , vol.8, no.1, pp.81-90, 2013 (Scopus) Sustainable Development

Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up.

Ocal G., ŞIKLAR Z., BERBEROĞLU M., Bilir P., Engiz O., FİTOZ Ö. S., et al.

Journal of clinical research in pediatric endocrinology , vol.1, no.1, pp.38-42, 2008 (Scopus) Sustainable Development

Obez çocuklarda risk faktörlerinin değerlendirilmesi

TUNA KIRSAÇLIOĞLU C., ŞIKLAR Z., Ünsal R., Dallar Y.

TURKIYE KLINIKLERI PEDIATRI , vol.12, pp.169-175, 2003 (Peer-Reviewed Journal)

Evaluation of different dose HCG treatments in undescended testis

TAŞAR M. A., ŞIKLAR Z., ÇELİKER İ. M., ÜNSAL R., ERDEVE Ö., DALLAR Y.

Gülhane Tıp Dergisi , vol.45, no.1, pp.58-63, 2003 (Scopus)

Ocak ve Haziran ayları arasında görülen 140 kızamıklı olgunun değerlendirilmesi

Tıraş Ü., TUNA KIRSAÇLIOĞLU C., ŞIKLAR Z., Dallar Y.

TURKIYE KLINIKLERI PEDIATRI , vol.11, pp.181-185, 2002 (Peer-Reviewed Journal)

Çocukluk çağı üst solunum yolu enfeksiyonlarında nimesulid ve parasetamolün antipiretik ve anti enflamatuvar etkilerinin karşılaştırılması

ŞIKLAR Z., Dallar Y., Tanyer G., TEKİNER A. S.

İlaç ve Tedavi Dergisi , vol.13, no.1, pp.23-28, 2000 (Peer-Reviewed Journal)

Refereed Congress / Symposium Publications in Proceedings

GATA4 VE NR5A1 MUTASYONU: YAKIN ILIŞKI, BENZER FENOTIP

Şıklar Z., Kızılcan Çetin S., Özsu E., Aycan Z.

28.Ulusal pediatrik Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.138

Comparison of Steroid Hormone Levels Measured by Immunoassay and Liquid Chromatography-Mass Spectrometry (LC-MS) Methods in the Follow-Up of Patients with Congenital Adrenal Hyperplasia

Özsu E., Şıklar Z., Kızılcan Çetin S., Doğan Ö., Aycan Z., Berberoğlu M.

The 62nd Annual ESPE Meeting 2024, Liverpool, England, 16 - 18 November 2024, pp.476

Evaluation of Copeptin Level in Children and Adolescents Monitored with Central Diabetes Incipidus

Özsu E., Doğan Ö., Şıklar Z., Kızılcan Çetin S., Aycan Z., Berberoğlu M.

The 62nd Annual ESPE Meeting 2024, Liverpool, England, 16 - 18 November 2024, pp.315-316

Molecular Characterization of Childhood Thyroid Nodules and Thyroid Cancer with DNA/RNA Next Generation Sequencing and Investigation of Phenotype-Genotype Correlation

Aycan Z., Kızılcan Çetin S., Ceyhan K., Şıklar Z., Berberoğlu M., Özsu E., et al.

The 62nd Annual ESPE Meeting 2024, Liverpool, England, 16 - 18 November 2024, pp.75

SENDROMIK SGA OLGULARINDA NADIR BIR TANI: SHORT SENDROMU

Dikmen İ., Özsu E., Türktan İ., Şıklar Z., Aycan Z., Mutlu H., et al.

28.ULUSAL ÇOCUK ENDOKRİNOLOJİ VE DİYABET KONGRESİ , Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.1-415

HIPERTIROIDI TANISI ALAN OLGULARIMIZIN BAŞVURU VE IZLEM ÖZELLIKLERININ BELIRLENMESI

Yüceer C., Berberoğlu M., Ceran A., Özsu E., Demirtaş Ş., Aycan Z., et al.

28.ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ , Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.1-451

FOLIKÜLER KARSINOMA ZEMININDE AZ DIFERANSIYE TIROID KANSERI GELIŞEN SOMATIK DICER1 MUTASYONUNA SAHIP BIR OLGU

Türktan İ., Sak S., Özsu E., Şıklar Z., Aycan Z., Abseyi N., et al.

28. ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET , Girne, Cyprus (Kktc), 30 April - 01 May 2024, pp.1-415

Çok Merkezli Olarak Çocukluk Yaş Grubunda Tanı Alan Kraniofaringiomalı Olguların Değerlendirilmesi

Şıklar Z., Özsu E., Özen S., Çizmecioğlu Jones F. M., Kızılcan Çetin S., Aycan Z., et al.

27. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi,, Antalya, Turkey, 2 - 07 May 2023, pp.1-200

ÇOCUKLUK ÇAĞINDA INVAZIF SEYIRLI NADIR BIR KANSER: DIFFÜZ SKLEROZAN VARYANT PAPILLER TIROID KARSINOMU

Demirtaş Ş., Şıklar Z., Kızılcan Çetin S., Özsu E., Aycan Z., Berberoğlu M.

28.Ulusal pediatrik Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.243

SANTRAL HIPOTIROIDI ILE BAŞVURAN VE PROP1 GEN MUTASYONU İLIŞKILI ÇOKLU HIPOFIZ HORMON EKSIKLIĞI TANISI ALAN ÜÇ KARDEŞ OLGUNUN UZUN DÖNEM İZLEMI

Şıklar Z., Özsu E., Kızılcan Çetin S., Demirtaş Ş., Aycan Z., Berberoğlu M.

28.Ulusal pediatrik Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.382

GONADAL DISGENEZI OLGUSUNDA BEKLENMEDIK BIR BIRLIKTELIK: RIT1 MUTASYONUNA SAHIP NOONAN SENDROMU

Demirtaş Ş., Kızılcan Çetin S., Şıklar Z., Özsu E., Aycan Z., Berberoğlu M.

28.Ulusal pediatrik Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.360

HETEROZİGOT CAAR MUTASYONU OLAN BİR VAKADA UZUN SÜRELİ SİNAKALSET TEDAVİ DENEYİMİ

Şıklar Z., Özsu E., Kızılcan Çetin S., Demirtaş Ş., Aycan Z., Berberoğlu M.

28.Ulusal pediatrik Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.370

RUSSEL-SILVER SENDROMLU OLGULARIN KLINIK ÖZELLIKLERI VE BÜYÜME HORMONU TEDAVI YANITLARI: ULUSAL ÇOK MERKEZLI ÇALIŞMA

Özgen İ. T., Kandemir T., Yıldız M., Poyrazoğlu Ş., Şıklar Z., Abseyi S. N., et al.

28. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi (UPEK), Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.90

Düşük Doğum Ağırlıklı Çocuklarda Büyüme Hormonu Tedavisi: Tek Merkez Büyüme Ve Final Boy Sonuçları

Şenyazar G., Şıklar Z., Aycan Z., Özsu E., Kızılcan Çetin S., Berberoğlu M.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 - 30 October 2022

T3 Predominant Graves’li Bir Olgu

Abseyi S. N., Şenyazar G., Şıklar Z., Özsu E., Demirtaş Ş., Türktan I., et al.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, , Antalya, Turkey, 2 - 07 May 2023, pp.335-336

Pediatrik Karaciğer Nakil Hastalarında Endokrinolojik Yan Etkilerin Değerlendirilmesi

Demirtaş Ş., Türktan İ., Kuloğlu Z., Şıklar Z., Kansu Tanca A., Aycan Z., et al.

27. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 2 - 07 May 2023, pp.88-89

Cushing Sendromu Bulguları ile Gelen bir Olgu: Hipofiz Adenomu mu? Rathke Kleft Kisti mi?

Türktan İ., Özsu E., Şıklar Z., Demirtaş Ş., Abseyi S. N., Aycan Z., et al.

27.Ulusal Pediatrik Endokrinoloji ve Diyabet kongresi, Antalya, Turkey, 2 - 07 May 2023, pp.360-361

ÇOCUKLUK ÇAĞI TIROID NODÜLLERINDE YENI NESIL DIZILEME ILE MUTASYON PROFILININ İNCELENMESI VE FENOTIP-GENOTIP KORELASYONUNUN ARAŞTIRILMASI

Aycan Z., Kızılcan Çetin S., Şıklar Z., Özsu E., Berberoğlu M.

28.Ulusal Çocuk Endokrinoloji ve Diyabet Kongresi, Girne, Cyprus (Kktc), 30 April - 05 May 2024, pp.383-384

Çoklu Endokrinolojik Sorunlar ve Disotonomili Bir Olgu: MIRAGE Sendromu

Kızılcan Çetin S., Şıklar Z., Özsu E., Aycan Z., Berberoğlu M.

27.Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi , Antalya, Turkey, 2 - 07 May 2023, pp.383-384

Nonklasik Konjenital Adrenal Hiperplazi Tanılı Olgularımızda Puberte Özelliklerinin Değerlendirilmesi

Şıklar Z., Özsu E., Kızılcan Çetin S., Demirtaş Ş., Aycan Z., Berberoğlu M.

Nonklasik Konjenital Adrenal Hiperplazi Tanılı Olgularımızda Puberte Özelliklerinin Değerlendirilmesi , Antalya, Turkey, 2 - 07 May 2023, pp.1-200

MAP3K7 Noonan Sendromu için Aday Gen Olabilir mi?: Olgu Sunumu

Kızılcan Çetin S., Şıklar Z., Özsu E., Aycan Z., Berberoğlu M.

MAP3K7 Noonan Sendromu için Aday Gen Olabilir mi?: Olgu Sunumu, Antalya, Turkey, 26 - 30 October 2022, pp.1-200

Birincil Osteoporozun Nadir Bir Nedeni: Osteogenez İmperfekta tip 15

Şıklar Z., Aycan Z., Özsu E., Kızılcan Çetin S., Berberoğlu M.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 - 30 October 2022, pp.1-200

Konjenital Adrenal Hiperplazi Dışı Primer ve Santral Adrenal Yetmezlikli Olguların Başvuru Özellikleri, Tedavi Bulgularının Değerlendirilmesi

Kızılcan Çetin S., Şıklar Z., Özsu E., Aycan Z., Demirtaş Ş., Berberoğlu M.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi,, Antalya, Turkey, 26 - 30 October 2022

Hiponatremi ile Başvuran Bir Olgu: Konjenital Adrenal Hiperplazi mi? Aldosteron Sentaz Eksikliği mi?

Şenyazar G., Şıklar Z., Özsu E., Aycan Z., Ceran A., Kızılcan Çetin S., et al.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 26 - 30 October 2022, pp.1-200

Pediatrik Santral Hipotiroidi Hastalarının İzlemindeki Klinik Bulguları ve Laboratuvar Karakteris kleri

Demirtaş Ş., Şıklar Z., Özsu E., Aycan Z., Kızılcan Çetin S., Berberoğlu M.

26. Ulusal Pediyatrik Endokrinoloji ve Diyabet Kongresi, Ankara, Turkey, 26 - 30 October 2022, pp.1-200

HİPERPARATROİDİZMLİ BİR YENİDOĞANDA KALSİYUM DUYARLI RESEPTÖR GENİNDE TANIMLANMAYAN YENİ BİR MUTASYUM

KAHVECİOĞLU D., ATASAY F. B., BERBEROĞLU M., YILDIZ D., ÇAKIR U., AKDUMAN H., et al.

22. ULUSAL NEONATOLOJİ KONGRESİ, Turkey, 10 - 13 April 2014

Hiperparatiroidizmli bir yenidoğanda kalsiyum duyarlı reseptör geninde tanımlanan yeni bir mutasyon

KAHVECİOĞLU D., ATASAY F. B., BERBEROĞLU M., YILDIZ D., ÇAKIR U., AKDUMAN H., et al.

UNEKO-22, Turkey, 10 - 13 April 2014

Laparoskopik pankreatektomi uygulanan bir hiperinsülinemik hipoglisemi olgusu

OKULU E., MUNGAN AKIN İ., SAVAŞ ERDEVE Ş., HACIHAMDİOĞLU B., ŞIKLAR Z., BERBEROĞLU M., et al.

18. Ulusal Neonatoloji Kongresi, Turkey, 21 - 24 April 2010

Konjenital adrenal hiperplazi ile birlikte faktör 10 eksikliği: Olgu sunumu

OKULU E., MUNGAN AKIN İ., SAVAŞ ERDEVE Ş., HACIHAMDİOĞLU B., ŞIKLAR Z., BERBEROĞLU M., et al.

18. Ulusal Neonatoloji Kongresi, Turkey, 21 - 24 April 2010

Oral antidiyabetik ile tedavi edilen in-vitro fertilizasyon sonucu doğmuş bir prematüre neonatal diyabet vakası

MUNGAN AKIN İ., OKULU E., SAVAŞ ERDEVE Ş., HACIHAMDİOĞLU B., ŞIKLAR Z., BERBEROĞLU M., et al.

18. Ulusal Neonatoloji Kongresi, Turkey, 21 - 24 April 2010

Yenidoğanda santral diabet insipitus: Oral desmopresin tedavisi uygulanan altı vaka

ATASAY F. B., BERBEROĞLU M., ARSAN S., ERDEVE Ö., MUNGAN AKIN İ., OKULU E., et al.

17. Ulusal Neonatoloji Kongresi, Turkey, 27 - 30 April 2009

A new concept for visceral leiahmaniasis: hypertrigliseridemi

ŞIKLAR Z., ERDEVE Ö., TAŞAR M. A., Tıraş Ü., Dallar Y.

3. World Congress of Pediatric İnfectious Diseases, Santiago, Chile, 02 November 2002

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