Doç.Dr. ENGİN KÖSE

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Long-term clinical evaluation of patients with alpha-mannosidosis – A multicenter study

KÖSE E., KASAPKARA Ç. S., İNCİ A., YILDIZ Y., SÜRÜCÜ KARA İ., Kahraman A. B., et al.

European Journal of Medical Genetics , cilt.68, 2024 (SCI-Expanded)

Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review

Kartal G. S., Yekedüz M. K., KÖSE E., EMİNOĞLU F. T.

Journal of Pediatric Endocrinology and Metabolism , cilt.37, sa.3, ss.260-270, 2024 (SCI-Expanded)

Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GNR gene: case report and review of literature

Kara I. S., KÖSE E., Cavdarli B., Eminoglu F. T.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.37, sa.3, ss.280-288, 2024 (SCI-Expanded)

Evaluation of the efficacy and associated complications of regional citrate anticoagulation in neonates: experience from a fourth level neonatal intensive care unit.

Köstekci Y. E., Kendirli T., Gün E., Uçmak H., Demirtaş F., Havan M., et al.

European journal of pediatrics , cilt.182, sa.11, ss.4897-4908, 2023 (SCI-Expanded)

IGAm: A novel index predicting long-term survival in patients with early-diagnosed inherited metabolic disorders.

Koç Yekedüz M., Köse E., Eminoğlu F. T.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.36, sa.11, ss.1100-1108, 2023 (SCI-Expanded)

A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity.

Sürücü Kara İ., Köse E., Koç Yekedüz M., Eminoğlu F. T.

Journal of pediatric endocrinology & metabolism : JPEM , 2023 (SCI-Expanded)

Ketogenic diet-responsive drug-resistant epilepsy in a case of asparagine synthetase deficiency with a novel compound heterozygous missense variant

Altıntaş M., YILDIRIM M., Uçar Ç. İ., KÖSE E., BEKTAŞ Ö., TEBER S.

Clinical Neurology and Neurosurgery , cilt.230, 2023 (SCI-Expanded)

A novel mutation in a patient with KIDAR syndrome: tenth patient in the literature

ALTINER Ş., Yurtdas K., DOĞULU N., KÖSE E., EMİNOĞLU F. T., KARABULUT H. G.

EUROPEAN JOURNAL OF HUMAN GENETICS , ss.238, 2023 (SCI-Expanded)

Co-Occurring Atypical Galactosemia and Wilson Disease

Dogulu N., Köse E., Tuna Kırsaçlıoğlu C., Ezgue F. S., Kuloğlu Z., Kansu A., et al.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.5, ss.454-458, 2022 (SCI-Expanded)

Early neuroimaging findings of infants diagnosed with inherited metabolic disorders in neonatal period: A case-control study

Koç Yekedüz M., Şen Akova B., KÖSE E., DOĞULU N., Öncül Ü., OKULU E., et al.

Clinical Neurology and Neurosurgery , cilt.222, 2022 (SCI-Expanded)

Pros and Cons of Telemedicine for Inherited Metabolic Disorders in a Developing Country During the COVID-19 Pandemic

Yekeduez M., DOĞULU N., SÜRÜCÜ KARA İ., Oncul U., BAKIRARAR B., KÜLLÜ P., et al.

TELEMEDICINE AND E-HEALTH , cilt.28, sa.11, ss.1604-1612, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Severe rhabdomyolysis in neuronal ceroid lipofuscinosis type 7

SÜRÜCÜ KARA İ., KÖSE E., DOĞULU N., Yuksel M. F., Ceylaner S., KENDİRLİ T., et al.

CLINICAL NEUROLOGY AND NEUROSURGERY , cilt.220, 2022 (SCI-Expanded)

Probable Miglustat-Induced Psychosis in a Child With Niemann-Pick Type C

Koc Yekeduz M., Oncul U., KÖSE E., EMİNOĞLU F. T.

CLINICAL NEUROPHARMACOLOGY , cilt.45, sa.4, ss.107-109, 2022 (SCI-Expanded)

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 , cilt.234, sa.4, ss.221-227, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Characteristics of continuous venovenous hemodiafiltration in the acute treatment of inherited metabolic disorders

EMİNOĞLU F. T., Oncul U., KAHVECİ F., OKULU E., Kraja E., KÖSE E., et al.

PEDIATRIC NEPHROLOGY , cilt.37, sa.6, ss.1387-1397, 2022 (SCI-Expanded)

Coexistence of Megaconial Congenital Muscular Dystrophy and Cystinuria: Mimicking Hypotonia-Cystinuria Syndrome

SÜRÜCÜ KARA İ., Oncul U., KÖSE E., Turan H. M., Ceylan A. C., EMİNOĞLU F. T.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.3, ss.240-245, 2022 (SCI-Expanded)

A Patient with Recurrent Severe Hypoglycemic Attacks and Mitochondrial Complex III Deficiency, Nuclear Type 3: a Novel UQCRB Variant

Yekeduz M. K., Oncul U., KÖSE E., Ezgu F., EMİNOĞLU F. T.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.1, ss.64-68, 2022 (SCI-Expanded)

ALG1-CDG: A Patient with a Mild Phenotype and Literature Review

Oncul U., KÖSE E., EMİNOĞLU F. T.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.1, ss.69-74, 2022 (SCI-Expanded)

Could lysosomal acid lipase enzyme activity be used for clinical follow-up in cryptogenic cirrhosis?

KÖSE E., Cagatay E., Yaras T., Kisa P. T., Guler S., Gulten Z. A., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.52, sa.4, ss.1075-1084, 2022 (SCI-Expanded)

Inherited metabolic disorders in the neonatal intensive care unit: Red flags to look out for

EMİNOĞLU F. T., Yekeduz M. K., DOĞULU N., Oncul U., KÖSE E., OKULU E., et al.

PEDIATRICS INTERNATIONAL , cilt.64, sa.1, 2022 (SCI-Expanded)

Serum biotin interference: A troublemaker in hormone immunoassays

Öncül Ü., EMİNOĞLU F. T., KÖSE E., DOĞAN Ö., Özsu E., AYCAN Z.

Clinical Biochemistry , cilt.99, ss.97-102, 2022 (SCI-Expanded)

Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises

Kisa P. T., Uzun O. U., Gunduz M., Bulbul F. S., KÖSE E., ARSLAN N.

Archives de Pediatrie , cilt.28, sa.8, ss.702-706, 2021 (SCI-Expanded)

The clinical variations and diagnostic challenges of deoxyguanosine kinase deficiency: a case series

Doğulu N., Tuna Kırsaçlıoğlu C., Köse E., Ünlüsoy Aksu A., Kuloğlu Z., Kansu Tanca A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.10, ss.1341-1347, 2021 (SCI-Expanded)

An Atypical Presentation of Mevalonate Kinase Deficiency in Response to Colchicine Treatment

Koc Yekeduz M., DOĞULU N., Oncul U., KÖSE E., Ceylaner S., EMİNOĞLU F. T.

MOLECULAR SYNDROMOLOGY , 2021 (SCI-Expanded)

A Mild Phenotype of Mitochondrial DNA Depletion Syndrome Type 13 with a Novel FBXL4 Variant

Oncul U., KÖSE E., EMİNOĞLU F. T.

MOLECULAR SYNDROMOLOGY , cilt.12, sa.5, ss.294-299, 2021 (SCI-Expanded)

Status dystonicus associated with CLN8 disease

YILDIRIM M., KÖSE E., Keceli A. M., Balasar O., Simsek N.

BRAIN & DEVELOPMENT , cilt.43, sa.4, ss.571-575, 2021 (SCI-Expanded)

Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey

Kose M., KÖSE E., Unalp A., Yilmaz U., Edizer S., Tekin H. G., et al.

NEUROLOGICAL SCIENCES , cilt.42, sa.3, ss.1103-1111, 2021 (SCI-Expanded)

The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

Kose M., IŞIK E., AYKUT A., DURMAZ A., KÖSE E., Ersoy M., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.4, ss.417-430, 2021 (SCI-Expanded)

Pyruvate carboxylase deficiency type C as a differential diagnosis of diabetic ketoacidosis

DOĞULU N., Oncul U., KÖSE E., AYCAN Z., EMİNOĞLU F. T.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.34, sa.7, ss.947-950, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey

Kose M., CANDA E., Kagnici M., AYKUT A., Adebali O., DURMAZ A., et al.

MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.25, 2020 (SCI-Expanded)

Transcobalamin II deficiency in twins with a novel variant in the TCN2 gene: case report and review of literature

KÖSE E., BESCİ Ö., Gudeloglu E., Suncak S., Oymak Y., Ozen S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.11, ss.1487-1499, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Analysis of the alpha galactosidase gene: mutation profile and description of two novel mutations with extensive literature review in Turkish population

Onay H., Bolat H., KILIÇ YILDIRIM G., KÖSE E., Ucar S. K., AŞIKOVALI S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.10, ss.1245-1250, 2020 (SCI-Expanded)

Cascade screening and treatment of children with familial hypercholesterolemia in Turkey

KÖSE E., Kose M., Ozturk S. I., Ozcan E., Onay H., Ozkan B.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.10, ss.1251-1256, 2020 (SCI-Expanded)

Functional vitamin B12 deficiency in phenylketonuria patients and healthy controls: An evaluation with combined indicator of vitamin B12 status as a biochemical index

Akış M., Kant M., Işık İ., Kısa P. T., Köse E., ARSLAN N., et al.

Annals of Clinical Biochemistry , cilt.57, sa.4, ss.291-299, 2020 (SCI-Expanded)

Different clinical presentation in a patient with two novel pathogenic variants of the FBXL4 gene

KÖSE E., Kose M., Edizer S., Akisin Z., Yilmaz Z. B., Sahin A., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.4, ss.652-656, 2020 (SCI-Expanded)

Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays

Paketçi A., Köse E., Gürsoy Çalan Ö., Acar S., Teke P., Demirci F., et al.

Hormone Research in Paediatrics , cilt.92, sa.2, ss.92-98, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical and molecular characteristics and time of diagnosis of patients with classical galactosemia in an unscreened population in Turkey

Teke Kisa P., Kose M., Unal O., Er E., ÖZTÜRK HİŞMİ B., Bulbul F. S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.32, sa.7, ss.675-681, 2019 (SCI-Expanded)

Vitamin/mineral and micronutrient status in patients with classical phenylketonuria

Kose E., ARSLAN N.

CLINICAL NUTRITION , cilt.38, sa.1, ss.197-203, 2019 (SCI-Expanded)

Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant

Gürsoy S., Ataman E., Bozkaya Ö. G., Köse E., Ayanoğlu M., Polat A. İ., et al.

PEDIATRICS AND NEONATOLOGY , cilt.59, sa.6, ss.632-633, 2018 (SCI-Expanded)

Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation

Kose E., ARMAĞAN C., Teke Klsa P., Onay H., Arslan N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.31, sa.11, ss.1289-1293, 2018 (SCI-Expanded)

First report of carglumic acid in a patient with citrullinemia type 1 (argininosuccinate synthetase deficiency)

Kose E., Kuyum P., Aksoy B., Häberle J., Arslan N., Öztürk Y.

JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS , cilt.43, sa.1, ss.124-128, 2018 (SCI-Expanded)

The Effects of Breastfeeding in Infants With Phenylketonuria

Kose E., Aksoy B., Kuyum P., Tuncer N., ARSLAN N., ÖZTÜRK Y.

JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES , cilt.38, ss.27-32, 2018 (SCI-Expanded)

Analysis of hematological parameters in patients treated with ketogenic diet due to drug-resistant epilepsy

Kose E., Guzel O., ARSLAN N.

NEUROLOGICAL SCIENCES , cilt.39, sa.1, ss.85-89, 2018 (SCI-Expanded)

Serum Level of Biotin Rather Than the Daily Dose Is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency

Paketci A., Kose E., GÜRSOY DORUK Ö., Acar S., Teke P., Demirci F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.613, 2018 (SCI-Expanded)

Identification of three novel mutations in fourteen patients with citrullinemia type 1

Kose E., Unal O., Bulbul S., Gunduz M., Häberle J., ARSLAN N.

CLINICAL BIOCHEMISTRY , cilt.50, sa.12, ss.686-689, 2017 (SCI-Expanded)

The Effect of Ketogenic Diet on Serum Selenium Levels in Patients with Intractable Epilepsy

ARSLAN N., Kose E., Guzel O.

BIOLOGICAL TRACE ELEMENT RESEARCH , cilt.178, sa.1, ss.1-6, 2017 (SCI-Expanded)

Changes of thyroid hormonal status in patients receiving ketogenic diet due to intractable epilepsy

Kose E., Guzel O., DEMİR K., ARSLAN N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.30, sa.4, ss.411-416, 2017 (SCI-Expanded)

A novel mutation in the glycine decarboxylase gene in patient with non-ketotic hyperglycinemia

Kose E., YİŞ U., Hiz S., ARSLAN N.

NEUROSCIENCES , cilt.22, sa.2, ss.131-133, 2017 (SCI-Expanded)

Is ketogenic diet treatment hepatotoxic for children with intractable epilepsy?

ARSLAN N., Guzel O., Kose E., Yılmaz U., Kuyum P., Aksoy B., et al.

SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , cilt.43, ss.32-38, 2016 (SCI-Expanded)

The Effect of Rapid Antigen Detection Test on Antibiotic Prescription Decision of Clinicians and Reducing Antibiotic Costs in Children with Acute Pharyngitis

Kose E., Kose S. S., Akca D., Yildiz K., Elmas C., Baris M., et al.

JOURNAL OF TROPICAL PEDIATRICS , cilt.62, sa.4, ss.308-315, 2016 (SCI-Expanded)

Atypical clinical manifestations of hepatitis a among children aged 1-16 years in South-Eastern region of Turkey

Yılmaz-Çiftdoğan D., Köse E., Aslan S., Gayyurhan E.

Turkish Journal of Pediatrics , cilt.57, sa.4, ss.339-344, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Henoch-Schonlein Purpura in Two Pediatric Patients Presenting as Terminal Ileitis

Kanik A., Kose E., Baran M., Sirin Kose S., Eliacik K., Sayan A., et al.

DIGESTIVE DISEASES AND SCIENCES , cilt.60, sa.1, ss.269-271, 2015 (SCI-Expanded)

Clinical and Economic Results of Ventriculoperitoneal Shunt Infections in Children

Kanik A., Sirin S., Kose E., Eliacik K., Anil M., Helvaci M.

TURKISH NEUROSURGERY , cilt.25, sa.1, ss.58-62, 2015 (SCI-Expanded)

Severe Acute Disseminated Encephalomyelitis With Clinical Findings of Transverse Myelitis After Herpes Simplex Virus Infection

Sarioglu B., Kose S. S., Saritas S., Kose E., Kanik A., Helvaci M.

JOURNAL OF CHILD NEUROLOGY , cilt.29, sa.11, ss.1519-1523, 2014 (SCI-Expanded)

Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case report

Kose E., Sirin Kose S., Alparslan C., Kasap Demir B., BERDELİ A., Mutlubas Ozsan F., et al.

RENAL FAILURE , cilt.36, sa.5, ss.808-810, 2014 (SCI-Expanded)

Do Pre-Transplant Stable Systolic Cardiac Functions Play A Role On Short-Term Systolic Cardiac Functions After Kidney Transplantation in Children?

Aksu N., Yavascan O., Alparslan C., Kose E., Tugmen C., Kilinc S., et al.

PEDIATRIC NEPHROLOGY , cilt.28, sa.8, ss.1648, 2013 (SCI-Expanded)

Spontaneous Resolution of Low-Grade Vesicoureteral Reflux in Children

Kose E., Alparslan C., Saritas S., Elmas C., Ozsan F. M., Yavascan O., et al.

PEDIATRIC NEPHROLOGY , cilt.28, sa.8, ss.1391, 2013 (SCI-Expanded)

Severe Renal Osteodystrophy in a Pediatric Patient With End-Stage Renal Disease: Sagliker Syndrome?

Yavascan O., Kose E., Alparslan C., Sirin Kose S., Bal A., Kanik A., et al.

JOURNAL OF RENAL NUTRITION , cilt.23, sa.4, ss.326-330, 2013 (SCI-Expanded)

An Opportunistic Pathogen in a Peritoneal Dialysis Patient: Ochrobactrum Anthropi

Alparslan C., Yavascan O., Kose E., Sanlioglu P., Aksu N.

INDIAN JOURNAL OF PEDIATRICS , cilt.80, sa.1, ss.72-74, 2013 (SCI-Expanded)

The effect of circumcision on the frequency of urinary tract infection, growth and nutrition status in infants with antenatal hydronephrosis

Kose E., Yavascan O., Turan O., Kangin M., Bal A., Alparslan C., et al.

RENAL FAILURE , cilt.35, sa.10, ss.1365-1369, 2013 (SCI-Expanded)

The performance of acute peritoneal dialysis treatment in neonatal period

Alparslan C., Yavascan O., Bal A., Kose E., Kanik A., Aksu N.

PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1802-1803, 2012 (SCI-Expanded)

Graft Survival in Pediatric Renal Transplanlantation: A 15-year experience in a single center

Alparslan C., Bal A., Kose E., Yavascan O., Aksu N., Gencer I., et al.

PEDIATRIC NEPHROLOGY , cilt.27, sa.9, ss.1826, 2012 (SCI-Expanded)

The Performance of Acute Peritoneal Dialysis Treatment in Neonatal Period

Alparslan C., Yavascan O., Bal A., Kanik A., Kose E., Demir B. K., et al.

RENAL FAILURE , cilt.34, sa.8, ss.1015-1020, 2012 (SCI-Expanded)

The influence of treatment on clinical outcome in mild and moderate forms of Henoch-Schoenlein purpura nephritis

Kasap B., Kose E., Alparslan C., Bal A., Yavascan O., Aksu N.

PEDIATRIC NEPHROLOGY , cilt.26, sa.9, ss.1657-1658, 2011 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

A Case of Late-Presenting Methylmalonic Acidemia from a Country Without Extended Newborn Screening

ÖZTÜRK A. G., Altınbezer P., KOÇ YEKEDÜZ M., KÖSE E., KENDİRLİ T., EMİNOĞLU F. T.

Ankara Üniversitesi Tıp Fakültesi Mecmuası , cilt.76, 2023 (Hakemli Dergi)

Mild congenital myopathy due to a novel variation in SPEG gene

YILDIRIM M., Balasar O., KÖSE E., Dogan M. T.

INTRACTABLE & RARE DISEASES RESEARCH , cilt.10, sa.3, ss.220-222, 2021 (ESCI)

Outcomes of Dyslipidemia Screening Program in School-aged Children

KÖSE E., Kose M., Topcu S., Matur B., Baris B., Ozkan B.

JOURNAL OF PEDIATRIC RESEARCH , cilt.8, sa.2, ss.155-160, 2021 (ESCI)

A case with Gaucher disease unable to reach enzyme replacement therapy because of COVID-19 quarantine: The first case from Turkey

Yekeduz M. K., KÖSE E., EMİNOĞLU F. T.

TURKISH ARCHIVES OF PEDIATRICS , cilt.56, sa.3, ss.270-271, 2021 (ESCI) Sürdürülebilir Kalkınma

Clinical and Molecular Features of Our Pompe Patients: Single-Center Experience

Kose M., Kose E., Kagnici M., Unalp A., Yilmaz U., Yilmaz M. M., et al.

MEDICAL JOURNAL OF BAKIRKOY , cilt.16, sa.1, ss.49-55, 2020 (ESCI)

Congenital Disorder of Glycosylation: Clinical and Molecular Characteristics of 9 Patients from Turkey

Kose M., Kose E., Kagnici M., Tekin H. G., Ozen B., Ozdemir T. R., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.10, sa.3, ss.267-273, 2020 (ESCI)

Knowledge of Primary Care Physicians on Lysosomal Storage Disorders

Kose E., Bulbul S., ARSLAN N.

JOURNAL OF PEDIATRIC RESEARCH , cilt.6, sa.4, ss.292-298, 2019 (ESCI)

The Effect of Phenylalanine Restricted Diet on Anthropometric Parameters in Classical Phenylketonuria Patients

Kose E., Ozturk H., Ozdemir B., Ozcelik R. E., Ciftci L., Cetin K., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.9, sa.1, ss.29-33, 2019 (ESCI)

The Effect of Large Neutral Amino Acids on Blood Phenylalanine Levels in Patients with Classical Phenylketonuria

TEKE KISA P., KÖSE E., Ören N., ARSLAN N.

JOURNAL OF BASIC AND CLINICAL HEALTH SCIENCES , cilt.1, sa.3, ss.79-81, 2017 (ESCI)

Evaluation of Demographic and Clinical Characteristics of Patients with Mucopolysaccharidosis

TEKE KISA P., KÖSE E., ATEŞOĞLU M., ARSLAN N.

JOURNAL OF PEDIATRIC RESEARCH , cilt.4, sa.2, ss.59-62, 2017 (ESCI)

A Baby Developing Digoxin Poisoning in Pediatric Intensive Care Unit: A Case Report

ANIL A. B., ulaş k., KÖSE E., doğan a., anıl m.

Turkish Journal of Pediatric Emergency and Intensive Care Medicine , cilt.2, sa.1, ss.35-40, 2015 (Hakemli Dergi)

Antineutrophil Cytoplasmic Antibody-Positive Glomerulonephritis Associated with Long-Term Propylthiouracil Treatment in Children

KÖSE E., yegül gülnar g., ŞİRİN KÖSE S., arıcı z. s., ergin m., ÇATLI G., et al.

JOURNAL OF PEDIATRIC RESEARCH , cilt.1, sa.4, ss.222-225, 2014 (ESCI)

The Diagnosis of Familial Mediterranean Fever in a Child Presenting with Trauma Following Acute Abdomen

KÖSE E., gelmez g., ŞİRİN KÖSE S., ALPARSLAN C., ANIL M., YAVAŞCAN Ö., et al.

JOURNAL OF PEDIATRIC RESEARCH , cilt.1, sa.3, ss.161-163, 2014 (ESCI)

Acil Serviste Ileri Yaşam Destegi Uygulanan Çocuklarda Erken Mortalite Belirteçleri

ANIL M., KÖSE E., ANIL A. B., Yörükbay Kaplan S., BARIŞ M., YURTSEVEN A.

J Pediatr Emerg Intens Care Med , cilt.1, sa.1, ss.17-24, 2014 (Hakemli Dergi)

Risk Factors for Hospital-Acquired Infection in Pediatric Intensive Care Unit

ANIL A. B., anıl m., önal özdemir n., bayram n., zümrüt ş. b., KÖSE E., et al.

Turkish Journal of Pediatric Emergency and Intensive Care Medicine , cilt.1, sa.1, ss.9-16, 2014 (Hakemli Dergi)

The Evaluation of the Patients Admitted to the Pediatric Emergency Department in a Training and Research Hospital

anıl m., ANIL A. B., KÖSE E., AKBAY S., helvacı m., aksu n.

Turkish Journal of Pediatric Emergency and Intensive Care Medicine , cilt.1, sa.2, ss.65-71, 2014 (Hakemli Dergi)

Percutaneous nephrostomy application in neonatal period: A case report

kanğın m., alparslan c., kahya m. o., ÇİTLENBİK H., KÖSE E., ÖZDEMİR T., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.3, sa.3, ss.215-218, 2013 (ESCI)

The effect of circumcision on urinary tract infection and growth in infants without any detected postnatal urinary tract abnormalities despite antenatal diagnosis of hydronephrosis

KÖSE E., ŞİRİN KÖSE S., pehlivan ö., alparslan c., kanğın m., cenkçi c. k., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.3, sa.1, ss.23-27, 2013 (ESCI)

Clinical and Laboratory Features of Hospitalized Children with Pandemic Influenza: Is it Different from the Other Respiratory Tract Infections?

şahbudak bal z., BAL A., anıl m., BAYRAM S. N., ARSLAN C. N., KÖSE E., et al.

JOURNAL OF PEDIATRIC INFECTION , cilt.6, sa.4, ss.144-148, 2012 (Scopus) Sürdürülebilir Kalkınma

B12 vitamin level in children and its relationship with complete blood count parameters

aydoğdu çolak a., anıl m., toprak b., KÖSE E., üstüner f.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.2, sa.2, ss.75-79, 2012 (ESCI)

A rapid response to steroid therapy in acute scrotum: A case of Henoch-Schönlein purpura

KANIK M. A., KÖSE E., ELİAÇIK K., ŞİRİN KÖSE S., ARSLAN C. N., HELVACI M.

Turkish Association of Pediatric Surgeons , cilt.26, ss.71-73, 2012 (Scopus)

Serum Sodium Levels in Children with Lower Respiratory Tract Infection

Anıl A. B., Anıl M., Köse E., Zengin N., Alparslan C., Bayram N., et al.

JOURNAL OF PEDIATRIC INFECTION , cilt.5, sa.3, ss.100-105, 2011 (ESCI)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

POMPE HASTALIĞINDA ALGLUKOSIDAZ ALFA DESENSITIZASYONU VE OMALIZUMAB DENEYIMI

SEVİNÇ S., DEVECİ N., HASKOLOĞLU Z. Ş., ERKMEN H., BASKIN A. K., DOĞULU N., et al.

29. ULUSAL ALERJİ VE KLİNİK İMMÜNOLOJİ KONGRESİ, Antalya, Türkiye, 29 Kasım 2023, cilt.1, ss.832

Hipoglisemiye metabolik yaklaşım

KÖSE E.

Ankara Pediatri Kongresi, Ankara, Türkiye, 09 Kasım 2023

Özel Diyetle Tedavi Edilen Karbonhidrat Metabolizma Bozukluklarında Nutrisyonel Değerlendirilmesi.

KOÇ YEKEDÜZ M., KÖSE E., EMİNOĞLU F. T.

1.Ulusal Çocuk Beslenme Kongresi, Gaziantep, Türkiye, 25 - 29 Ekim 2023

Proteinden Kısıtlı Diyet Alan Kalıtsal Metabolik Hastalık Tanılı Hastalarda Nutrisyonel Parametrelerin Değerlendirilmesi.

SÜRÜCÜ KARA İ., KOÇ YEKEDÜZ M., KÖSE E., EMİNOĞLU F. T.

1.Ulusal Çocuk Beslenme Kongresi, Gaziantep, Türkiye, 25 - 29 Ekim 2023

Fenilketonüri Tanı Tedavi ve Takibinde Yapay Zeka (ChatGPT)

KOÇ YEKEDÜZ M., KÖSE E.

67. Türkiye Milli Pediatri Kongresi, Girne, Kıbrıs (Kktc), 18 - 22 Ekim 2023

Erken Teşhis Edilen Kalıtsal Metabolik Hastalığı Olan Hastalarda Uzun Süreli Sağkalımı Öngören Yeni Bir İndeks: IGAm-İndeks.

KOÇ YEKEDÜZ M., KÖSE E., EMİNOĞLU F. T.

67. Türkiye Milli Pediatri Kongresi, Girne, Kıbrıs (Kktc), 18 - 22 Ekim 2023

IGAm Index Predicts Long-term Survival in Patients with Early-diagnosed Inherited Metabolic Disorders

KOÇ YEKEDÜZ M., KÖSE E., EMİNOĞLU F. T.

SSIEM Annual Symposium 2023, Kudus, Endonezya, 29 Ağustos - 01 Kasım 2023

Investigation of mitochondrial DNA depletion syndromes in children under 5 years old with acute liver manifestations of unknown etiology.

EMİNOĞLU F. T., KÖSE E., CEYLANER S., KASAPKARA Ç. S., BOZACI A. E., CEYLANER G., et al.

SSIEM Annual Symposium 2023, Kudus, Endonezya, 29 Ağustos - 01 Eylül 2023

Evaluation of Repeated Biotinidase Enzyme Activity and The Effect of BTD Gene p.Asp444His Variant on Enzyme Activity and Clinical Findings.

SÜRÜCÜ KARA İ., KÖSE E., KOÇ YEKEDÜZ M., EMİNOĞLU F. T.

SSIEM Annual Symposium 2023, Kudus, Endonezya, 29 Ağustos - 01 Eylül 2023

Long-term Clinical Evaluation of Patients with Alpha-mannosidosis – A Multicenter Study

KÖSE E., KASAPKARA Ç. S., İNCİ A., YILDIZ Y., SÜRÜCÜ KARA İ., KAHRAMAN A. B., et al.

SSIEM Annual Symposium 2023, Kudus, Endonezya, 29 Ağustos - 01 Eylül 2023

Hipoglisemik Çocuğa Yaklaşım Metabolizma Hastalıkları Uzmanı Gözüyle

KÖSE E.

58. Türk Pediatri Kongresi, Kıbrıs (Kktc), 9 - 13 Mayıs 2023

Juvenil Metakromatik Lökodistrofi Tanılı Hastada Kemik İliği Nakli Tedavisi ve Gelişen Komplikasyonlar.

YAĞCİ G. N., SÜRÜCÜ KARA İ., KOÇ YEKEDÜZ M., DOĞULU N., KÖSE E., EMİNOĞLU F. T.

VIII. Uluslararası Katılımlı LizozomaI Hastalıklar Kongresi, Bursa, Türkiye, 3 - 07 Mayıs 2023

Klinik Bulguları Yenidoğan Döneminde Başlayan Nöronal Seroid Lipofusinozis 11 Vakası.

SÜRÜCÜ KARA İ., KOÇ YEKEDÜZ M., KAYNAK ŞAHAP S., KÖSE E., EMİNOĞLU F. T.

VIII. Uluslararası Katılımlı LizozomaI Hastalıklar Kongresi, Bursa, Türkiye, 3 - 07 Mayıs 2023

Alfa-Mannosidozlu Hastaların Uzun Süreli Klinik Değerlendirmesi: Çok Merkezli Bir Çalışma.

KÖSE E., KASAPKARA Ç. S., İNCİ A., YILDIZ Y., SÜRÜCÜ KARA İ., KAHRAMAN A. B., et al.

VIII. Uluslararası Katılımlı LizozomaI Hastalıklar Kongresi, Bursa, Türkiye, 3 - 07 Mayıs 2023

Glukoserebrozidaz enzim düzeyi analizi Gaucher hastalığı tanısı için yeterli midir? Geç tanı almış bir Gaucher Tip 3C Vakası.

KOÇ YEKEDÜZ M., SÜRÜCÜ KARA İ., KÖSE E., DEMİR Ö., EMİNOĞLU F. T.

VIII. Uluslararası Katılımlı LizozomaI Hastalıklar Kongresi, Bursa, Türkiye, 3 - 07 Mayıs 2023

Recent Advances in the Diagnosis and Treatment

KÖSE E.

APASL SINGLE TOPIC CONFERENCE 2022, İstanbul, Türkiye, 23 Eylül 2022

Miglustat-Induced Psychosis in a Child with Niemann-Pick Type C

KOÇ YEKEDÜZ M., ÖNCÜL Ü., KÖSE E., EMİNOĞLU F. T.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

An Alternative to Electrophysiological Study in the Diagnosis of Carpal Tunnel Syndrome in Patients with MPS: Wrist Ultrasonography

KÖSE E., KOÇ YEKEDÜZ M., İNCİ A., YÜKSEL M. F., DOĞULU N., ŞEN AKOVA B., et al.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

The Effect of Dietary Protein Content on Enteric Microbiota and Urine Organic Acids in Patients with Methylmalonic Acidemia

DOĞULU N., KÖSE E., Yolcu F., DOĞAN Ö., SEZERMAN O. U., EMİNOĞLU F. T.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

The Effect of Dietary Protein Content on Plasma Amino Acids and Appetite in Patients with Methylmalonic Acidemia

DOĞULU N., KÖSE E., Yolcu F., DOĞAN Ö., EMİNOĞLU F. T.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

Hypobetalipoproteinemia; Diagnosis that should be kept in mind in elevated transaminases and hepatosteatosis

KÖSE E., SÜRÜCÜ KARA İ., EMİNOĞLU F. T.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

Severe Rhabdomyolysis in Neuronal Ceroid Lipofuscinosis Type 7 Mimicking Chorea Acanthocytosis

EMİNOĞLU F. T., SÜRÜCÜ KARA İ., DOĞULU N., Şahin S., Sayar Y., KENDİRLİ T., et al.

SSIEM Annual Symposium 2022, Freiburg, Almanya, 30 Ağustos 2022

A novel mutation in a patient with KIDAR syndrome: tenth patient in the literature

ALTINER Ş., YURTDAŞ A. K., DOĞULU N., KÖSE E., EMİNOĞLU F. T., KARABULUT H. G.

European Human Genetics Conference, Viyana, Avusturya, 11 - 14 Haziran 2022

MPS Hastalarında Karpal Tünel Sendromunda Elektrofizyolojik Çalışmaya Alternatif: Bilek Ultrasonografisi

Koç Yükedüz M., KÖSE E., İNCİ A., YÜKSEL M. F., DOĞULU N., ŞEN AKOVA B., et al.

XVI. Uluslararası Katılımlı Metabolik Hastalıklar ve Beslenme Kongresi, Hatay, Türkiye, 28 Mayıs - 01 Haziran 2022