Prof. Dr. SERAP TEBER

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Bilateral striatal necrosis in a case with ADAR1-related Aicardi Goutieres Syndrome

YILDIRIM M., Tabanli F. P., BEKTAŞ Ö., TEBER S.

NEUROLOGICAL SCIENCES , 2025 (SCI-Expanded)

A Novel Variant of the CTSD Gene Associated with Juvenile-onset Neuronal Ceroid Lipofuscinosis Type 10: A Case Report and Literature Review.

Çiçek S., Yıldırım M., Tabanlı F. P., Köse E., Bektaş Ö., Teber S.

Cerebellum (London, England) , cilt.24, sa.1, ss.7, 2024 (SCI-Expanded)

Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study.

Kanmaz S., Tekgul H., Kayilioglu H., Atas Y., Kart P. O., Yildiz N., et al.

Seizure , cilt.123, ss.17-25, 2024 (SCI-Expanded)

Progressive Myoclonus Epilepsy and Beyond: A Systematic Review of SEMA6B-related Disorders.

Altintaş M., Yıldırım M., Bektaş Ö., Teber S.

Neuropediatrics , 2024 (SCI-Expanded)

Atlantoaxial Instability due to Os Odontoideum in a Child with Christianson Syndrome

Guven N. E., Ucmak H., Ucar C. I., HAVAN M., YILDIRIM M., TEBER S., et al.

MOLECULAR SYNDROMOLOGY , cilt.15, sa.5, ss.398-402, 2024 (SCI-Expanded)

Correlation between early computed tomography findings and neurological outcome in pediatric traumatic brain injury patients.

Şahin S., Botan E., Gün E., Yüksel M. F., Süt N. Y., Kartal A. T., et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology , cilt.45, sa.9, ss.4417-4425, 2024 (SCI-Expanded)

Management of neurological problems in children on home invasive mechanical ventilation.

Sayar Y., Yıldırım M., Teber S.

Pediatric pulmonology , cilt.59, sa.8, ss.2196-2202, 2024 (SCI-Expanded)

VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review.

Yıldırım M., Yarenci G. B., Genç M. B., Uçar Ç. İ., Bayav S., Tekin M. N., et al.

Neuropediatrics , cilt.55, sa.3, ss.200-204, 2024 (SCI-Expanded)

Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis?

Koç Yekedüz M., KÖSE E., İNCİ A., Yüksel M. F., DOĞULU N., Şen Akova B., et al.

Pediatric neurology , cilt.155, ss.171-176, 2024 (SCI-Expanded)

Metabolic etiologies in children with infantile epileptic spasm syndrome: Experience at a tertiary pediatric neurology center.

Yüksel M. F., Doğulu N., Yıldırım M., Köse E., Bektaş Ö., Eminoğlu F. T., et al.

Brain & development , cilt.46, sa.6, ss.213-218, 2024 (SCI-Expanded)

An infant with episodic stridor and respiratory crises since birth: A challenging diagnosis

ZİREK F., ÖZCAN G., TEKİN M. N., Ucar C. I., KARTAL A. T., BALABAN B., et al.

PEDIATRIC PULMONOLOGY , cilt.59, sa.4, ss.1067-1072, 2024 (SCI-Expanded)

Predictors of medical intractability in children with epilepsy onset during the first two years of life, excluding infantile epileptic spasm syndrome.

Yıldırım M., Altıntaş M., Uysal E., Bektaş Ö., Teber S.

Seizure , cilt.117, ss.206-212, 2024 (SCI-Expanded)

Investigating the Impact on Long-Term Outcomes and the Necessity of Hereditary Thrombophilia Screening in Presumed or Perinatal Arterial Ischemic Stroke

BEKTAŞ Ö., Goktas O. A., Atasay B., TEBER S.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.30, 2024 (SCI-Expanded)

A multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?

Yılmaz D., TEBER S., Gültutan P., YILDIRIM M., BEKTAŞ Ö., ALİKILIÇ D., et al.

Multiple Sclerosis and Related Disorders , cilt.79, 2023 (SCI-Expanded)

Subacute Sclerosing Panencephalitis: Magnetic Resonance Imaging Findings of a Rapidly Progressive Case

Tuncer G., Kutluk M., Albayrak P., TEBER S., Deda G.

Neurology India , cilt.71, sa.5, ss.1036-1037, 2023 (SCI-Expanded)

Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study

Sarıkaya Uzan G., Vural A., Yüksel D., Aksoy E., Öztoprak Ü., CANPOLAT M., et al.

Pediatric Neurology , cilt.145, ss.3-10, 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 Case of Multidrug-Resistant Lance-Adams Syndrome Successfully Treated With Phenobarbital.

Yeniay Süt N., Yıldırım M., Bektaş Ö., Kendirli T., Teber S.

Clinical neuropharmacology , cilt.46, sa.1, ss.34-37, 2023 (SCI-Expanded)

Chronic inflammatory demyelinating polyradiculoneuropathy associated with Sjögren’s syndrome in a child

Süt N. Y., KARTAL A. T., Ertem Ş., AYDIN F., YILDIRIM M., BEKTAŞ Ö., et al.

Turkish Journal of Pediatrics , cilt.65, sa.1, ss.155-160, 2023 (SCI-Expanded)

Seizure treatment with olfactory training: a preliminary trial

YILMAZ Y., TÜRK B. G., Ser M. H., YENİAY SÜT N., Sahin S., Yildiz E. P., et al.

NEUROLOGICAL SCIENCES , cilt.43, sa.12, ss.6901-6907, 2022 (SCI-Expanded)

Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome

YILDIRIM M., Oncel I., BEKTAŞ Ö., Tanali G., Sahin S., Kutluk T., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.41, ss.19-26, 2022 (SCI-Expanded)

Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

Yilmaz U., GÜCÜYENER K., Yavuz M., Oncel I., CANPOLAT M., Saltik S., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.41, ss.8-18, 2022 (SCI-Expanded)

Risk of seizure relapse and long-term outcomes after discontinuation of antiseizure medication in children with epilepsy

YILDIRIM M., BEKTAŞ Ö., KARTAL A. T., YENİAY SÜT N., TEBER S.

EPILEPSY & BEHAVIOR , cilt.134, 2022 (SCI-Expanded)

Early Neurologic Complications and Long-term Neurologic Outcomes of Extracorporeal Membrane Oxygenation Performed in Children

Azapagasi E., KENDİRLİ T., Tuncer G. O., Perk O., YILMAZ IŞIKHAN S., Tiras S., et al.

KLINISCHE PADIATRIE , cilt.234, sa.02, ss.96-104, 2022 (SCI-Expanded)

A Rare Pediatric Case of Severe Rhabdomyolysis Owing to Dual Infection

Goktas O. A., BEKTAŞ Ö., Tuncer G. O., ÖZÇAKAR Z. B., TALİM B., EMİNOĞLU F. T., et al.

KLINISCHE PADIATRIE , cilt.234, sa.02, ss.119-122, 2022 (SCI-Expanded)

The diagnostic challenges of congenital mirror movements and hand stereotypies in a case with TUBB3-associated tubulinopathy

YENİAY SÜT N., YILDIRIM M., BEKTAŞ Ö., ALTINTAŞ M., TEBER S.

ACTA NEUROLOGICA BELGICA , cilt.122, sa.1, ss.251-253, 2022 (SCI-Expanded)

A mobile app that uses neurofeedback and multi-sensory learning methods improves reading abilities in dyslexia: A pilot study

Eroglu G., TEBER S., Erturk K., Kirmizi M., Ekici B., Arman F., et al.

APPLIED NEUROPSYCHOLOGY-CHILD , cilt.11, sa.3, ss.518-528, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene

YILDIRIM M., BEKTAŞ Ö., Tuncez E., YENİAY SÜT N., Sayar Y., Oncul U., et al.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.2, ss.139-145, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Changes in EEG complexity with neurofeedback and multi-sensory learning in children with dyslexia: A multiscale entropy analysis

Eroglu G., Gurkan M., TEBER S., Erturk K., Kirmizi M., Ekici B., et al.

APPLIED NEUROPSYCHOLOGY-CHILD , cilt.11, sa.2, ss.133-144, 2022 (SCI-Expanded)

Horizontal Gaze Palsy with Progressive Scoliosis in an Infant Diagnosed Before Developing Scoliosis: MRI and DTI Findings

Ucan B., Kaynak Sahap S., Bako D., Tiras S., Ceylaner S., Fitoz S.

KLINISCHE PADIATRIE , cilt.234, sa.1, ss.52-55, 2022 (SCI-Expanded)

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study

Bozkaya-Yilmaz S., Karadag-Oncel E., OLGAÇ DÜNDAR N., GENÇPINAR P., Sarioglu B., Arican P., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.181, sa.1, ss.383-391, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Intracranial Calcification Associated with 3-Methylcrotonyl-CoA Carboxylase Deficiency

Sahin S., YILDIRIM M., BEKTAŞ Ö., SÜRÜCÜ KARA İ., Ceylan A. C., TEBER S.

MOLECULAR SYNDROMOLOGY , cilt.12, ss.393-398, 2021 (SCI-Expanded)

Hypomelanosis of Ito presenting with unilateral dilation of Virchow-Robin spaces: a case report

Ucar C. I., YILDIRIM M., Sayar Y., Sahin S., TEBER S.

CHILDS NERVOUS SYSTEM , cilt.37, sa.9, ss.2931-2934, 2021 (SCI-Expanded)

Motor functions, quality of life and maternal anxiety and depression in children with cerebral palsy of different intelligence levels

Akcay E., TANIR Y., Teber S., KILIÇ B. G.

TURKISH JOURNAL OF PEDIATRICS , cilt.63, sa.5, ss.846-854, 2021 (SCI-Expanded)

Therapeutic plasma exchange in clinical pediatric neurology practice: Experience from a tertiary referral hospital

YILDIRIM M., BEKTAŞ Ö., BOTAN E., Sahin S., Gurbanov A., TEBER S., et al.

CLINICAL NEUROLOGY AND NEUROSURGERY , cilt.207, 2021 (SCI-Expanded)

Genotype-Phenotype Correlation of the Childhood-Onset Bethlem Myopathy in the Mediterranean Region of Turkey.

Kutluk M. G., Kadem N., BEKTAŞ Ö., Randa N. C., Tuncer G. O., Albayrak P., et al.

Annals of Indian Academy of Neurology , cilt.24, sa.4, ss.547-551, 2021 (SCI-Expanded)

Tissue Plasminogen Activator Use in Pediatric Patients: A Single Center Experience

PEKPAK E., İNCE E., ERTEM M., Tutar E., Ileri T., UÇAR T., et al.

Journal of Pediatric Hematology/Oncology , cilt.43, sa.5, 2021 (SCI-Expanded)

A Novel PUS1 Mutation in 2 Siblings with MLASA Syndrome: A Review of the Literature

Oncul U., İNCE E., KULOĞLU Z., Teber-Tiras S., KAYGUSUZ G., EMİNOĞLU F. T.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.43, sa.4, 2021 (SCI-Expanded)

A Novel Variant of COL6A2 Gene Causing Bethlem Myopathy and Evaluation of Essential Hypertension

Kutluk M. G., Kadem N., BEKTAŞ Ö., Randa N. C., Tuncer G. O. Z., Albayrak P., et al.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , cilt.24, sa.2, ss.280-282, 2021 (SCI-Expanded)

Levetiracetam monotherapy in children with epilepsy: Experience from a tertiary pediatric neurology center

YILDIRIM M., BEKTAŞ Ö., Goktas O. A., Yuksel M. F., Sahin S., TEBER S.

EPILEPSY & BEHAVIOR , cilt.116, 2021 (SCI-Expanded)

Hashimoto's encephalopathy in children: different manifestations of five cases

Kutluk M. G., Haznedar P., BEKTAŞ Ö., Kadem N., Tuncer G. O., Albayrak P., et al.

ACTA NEUROLOGICA BELGICA , cilt.119, sa.4, ss.595-599, 2019 (SCI-Expanded)

Effects of levetiracetam and valproic acid treatment on liver function tests, plasma free carnitine and lipid peroxidation in childhood epilepsies

Haznedar P., DOĞAN Ö., Albayrak P., Tuncer G. O., TEBER S., Deda G., et al.

EPILEPSY RESEARCH , cilt.153, ss.7-13, 2019 (SCI-Expanded)

Hashimoto's encephalopathy presenting as pseudobulbar palsy

Tuncer G. O., TEBER S., Kutluk M. G., Albayrak P., Deda G.

CHILDS NERVOUS SYSTEM , cilt.34, sa.6, ss.1251-1254, 2018 (SCI-Expanded)

Complete paralytic botulism mimicking a deep coma in a child

Azapagasi E., KENDİRLİ T., Oz-Tuncer G., Albayrak P., TEBER S., Deda G.

TURKISH JOURNAL OF PEDIATRICS , cilt.59, sa.5, ss.581-585, 2017 (SCI-Expanded)

A celiac case mimicking mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

Aksoy E., TEBER S., Deda G.

TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.6, ss.662-665, 2016 (SCI-Expanded)

Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome)

Micalizzi A., Poretti A., Romani M., Ginevrino M., Mazza T., Aiello C., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.24, sa.9, ss.1262-1267, 2016 (SCI-Expanded)

Neurological findings spectrum in Celiac disease

Aksoy E., TEBER S., KANSU TANCA A., Deda G., Kartal A.

TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.3, ss.233-240, 2016 (SCI-Expanded)

Severe theophylline poisoning treated with continuous venovenous hemodialysis in a child

Yaman A., KENDİRLİ T., Odek C., Azapagasi E., Erkol H., PİŞKİN İ. E., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.3, ss.297-300, 2016 (SCI-Expanded)

Cerebral Sinovenous Thrombosis in Children and Neonates: Clinical Experience, Laboratory, Treatment, and Outcome

BEKTAŞ Ö., TEBER S., Akar N., Uysal L. Z., ARSAN S., Atasay B., et al.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.21, sa.8, ss.777-782, 2015 (SCI-Expanded)

Two children with steroid-responsive nephrotic syndrome complicated by cerebral venous sinus thrombosis

Kurt-Sukur E. D., ÖZÇAKAR Z. B., FİTOZ Ö. S., YILMAZ S., TEBER S., İNCE E., et al.

NEFROLOGIA , cilt.35, sa.5, ss.497-500, 2015 (SCI-Expanded)

Pseudotumor cerebri/idiopathic intracranial hypertension in children: An experience of a tertiary care hospital

Degerliyurt A., TEBER S., Karakaya G., Guven A., Seker E. D., Arhan E. P., et al.

BRAIN & DEVELOPMENT , cilt.36, sa.8, ss.690-699, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Panayiotopoulos syndrome: A case series from Turkey

Degerliyurt A., TEBER S., BEKTAŞ Ö., Senkon G.

EPILEPSY & BEHAVIOR , cilt.36, ss.24-32, 2014 (SCI-Expanded)

Busulfan triggers epileptic seizures under levetiracetam and valproic acid therapy

Erdem A. Y., Azik F., Tavil B., TEBER S., Tunc B., Uckan D.

PEDIATRIC TRANSPLANTATION , cilt.18, sa.4, ss.412-413, 2014 (SCI-Expanded)

Chloral hydrate and/or hydroxyzine for sedation in pediatric EEG recording

BEKTAŞ Ö., Arica B., TEBER S., Yilmaz A., Zeybek H., Kaymak S., et al.

BRAIN & DEVELOPMENT , cilt.36, sa.2, ss.130-136, 2014 (SCI-Expanded)

Electroencephalogram Variations in Pediatric Migraines and Tension-Type Headaches

Ozkan M., TEBER S., Deda G.

PEDIATRIC NEUROLOGY , cilt.46, sa.3, ss.154-157, 2012 (SCI-Expanded)

Childhood migraine and hypercoagulopathy

TEBER S., Akar N., Deda G.

BRITISH JOURNAL OF HAEMATOLOGY , cilt.155, sa.4, ss.527-528, 2011 (SCI-Expanded)

Lipoprotein A Levels in Pediatric Migraine

TEBER S., BEKTAŞ Ö., Yilmaz A., Aksoy E., Akar N., Deda G.

PEDIATRIC NEUROLOGY , cilt.45, sa.4, ss.225-228, 2011 (SCI-Expanded)

A challenging review of childhood incontinence: rare complications of dysfunctional elimination syndrome in an epileptic boy

Aydogdu O., BURGU B., TEBER S., Altugan S., Gokce I., Deda G., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.1, ss.100-103, 2011 (SCI-Expanded)

Fetal and neonatal cardiac rhabdomyomas: clinical presentation, outcome and association with tuberous sclerosis complex

Atalay S., Aypar E., UÇAR T., Altug N., Deda G., TEBER S., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.5, ss.481-487, 2010 (SCI-Expanded)

Congenital myotonic dystrophy associated with Moebius syndrome and double-outlet right ventricle

TEBER S., Sezer T., Aypar E., KENDİRLİ T., Atalay S., Deda G.

PEDIATRICS INTERNATIONAL , cilt.52, sa.3, ss.501-502, 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 , cilt.2, sa.2, ss.89-91, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Status epilepticus and capillary leak syndrome in a neonate related to perinatal hypoxic-ischemic encephalopathy

Karagol B. S., ERDEVE Ö., ARSAN S., Atasay B., Ekim M., TEBER S., et al.

INDIAN JOURNAL OF PEDIATRICS , cilt.77, sa.4, ss.439-441, 2010 (SCI-Expanded)

Lipoprotein (a) Levels in Childhood Arterial Ischemic Stroke

TEBER S., Deda G., Akar N., Soylu K.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.16, sa.2, ss.214-217, 2010 (SCI-Expanded)

FATAL FUNGAL ENDOCARDITIS DUE TO TRICHOSPORON ASAHII IN AN ADOLESCENT BOY

Aypar E., Atalay S., Tutar E., ÇİFTCİ E., Uysalel A., KENDİRLİ T., et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY , cilt.140, 2010 (SCI-Expanded)

Relationship between functional promoter polymorphism in the XBP1 gene (-116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemia

YILMAZ E., Akar R., Eker S., Deda G., Adiguzel Y., Akar N.

MOLECULAR BIOLOGY REPORTS , cilt.37, sa.1, ss.269-272, 2010 (SCI-Expanded)

The Relation Between Cytokines, Soluble Endothelial Protein C Receptor, and Factor VIII Levels in Turkish Pediatric Stroke Patients

Yururer D., TEBER S., Deda G., Egin Y., Akar N.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.15, sa.5, ss.545-551, 2009 (SCI-Expanded)

Childhood optic neuritis: The pediatric neurologist's perspective

Cakmakli G., Kurne A., Guven A., Serdaroglu A., Topaloglu H., TEBER S., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.13, sa.5, ss.452-457, 2009 (SCI-Expanded)

Response

Ünal Ö., Deda G., TEBER S., ERTEM M., Akar N.

Pediatric Neurology , cilt.41, sa.1, ss.78-79, 2009 (SCI-Expanded)

Assessment of Citrullinated Myelin by H-1-MR Spectroscopy in Early-Onset Multiple Sclerosis

Oguz K. K., Kurne A., Aksu A. O., KARABULUT E., Serdaroglu A., TEBER S., et al.

AMERICAN JOURNAL OF NEURORADIOLOGY , cilt.30, sa.4, ss.716-721, 2009 (SCI-Expanded)

A note on Homocysteine levels in Children

Tras S., Deda G., Akar N.

THROMBOSIS RESEARCH , cilt.123, sa.5, ss.799, 2009 (SCI-Expanded)

Thrombophilic Risk Factors in Epileptic Children Treated with Valproic Acid

Uenal O., Deda G., TEBER S., ERTEM M., Akar N.

PEDIATRIC NEUROLOGY , cilt.40, sa.2, ss.102-106, 2009 (SCI-Expanded)

Protein Z G79A polymorphism in Turkish pediatric cerebral infarct patients

Öztürk A., Eǧin Y., Deda G., TEBER S., Akar N.

Turkish Journal of Hematology , cilt.25, sa.3, ss.133-135, 2008 (SCI-Expanded)

Severe muscle-eye-brain disease is associated with a homozygous mutation in the POMGnT1 gene

TEBER S., Sezer T., Kafalt M., Manzini M. C., Yuksel B. K., Tekin M., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.12, sa.2, ss.133-136, 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 , cilt.75, sa.2, ss.186-188, 2008 (SCI-Expanded)

Juvenile form of myasthenia gravis presenting as recurrent pulmonary infection with atelectasis

Unal O., TEBER S., Kendirli T., Deda G., Anlar B.

PEDIATRICS INTERNATIONAL , cilt.49, sa.6, ss.1007-1008, 2007 (SCI-Expanded)

T102C polymorphism of the serotonin (5-HT) 2A receptor gene in Turkish children with cerebral infarct

Dönmez B. N., TEBER S., Deda G., Akar N.

Turkish Journal of Hematology , cilt.24, sa.1, ss.14-17, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients

Ulu A., Gunal D., Tiras S., Egin Y., Deda G., Akar N.

THROMBOSIS RESEARCH , cilt.120, sa.1, ss.47-52, 2007 (SCI-Expanded)

Depression and anxiety semptom severity in a group of children with epilepsy and related factors

Bilgic A., Yilmaz S., Tiras S., Deda G., Kilic E. Z.

TURK PSIKIYATRI DERGISI , cilt.17, sa.3, ss.165-172, 2006 (SSCI)

Pediatric stroke, homocysteine and MTHFR 677C-T and 1298 A-C

Akar N., Deda G., TEBER S.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.28, sa.9, ss.632-633, 2006 (SCI-Expanded)

Hypertension induced reversible posterior leukoencephalopathy syndrome: a report of two cases

ÖZÇAKAR Z. B., Ekim M., FİTOZ Ö. S., TEBER S., Hizel S., Acar B., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.163, sa.12, ss.728-730, 2004 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

An Unusual Presentation of Infantile Epileptic Spasm Syndrome in a Child

Yıldırım M., Akyol Özkara K., Çiçek S., Bektaş Ö., Teber S.

TURKISH ARCHIVES OF PEDIATRICS , cilt.59, sa.6, ss.603-604, 2024 (ESCI)

Periodic Lateralized Epileptiform Discharges: A Child with a Rare Manifestation of Posterior Reversible Encephalopathy Syndrome and Literature Review

YILDIRIM M., ÇİÇEK S., HAVAN M., KENDİRLİ T., TEBER S.

Turkish Archives of Pediatrics , cilt.59, sa.3, ss.321-324, 2024 (ESCI)

A sydenham chorea attack associated with COVID-19 infection

YÜKSEL M. F., YILDIRIM M., BEKTAŞ Ö., ŞAHİN S., TEBER S.

Brain, Behavior, & Immunity - Health , cilt.13, 2021 (Hakemli Dergi) Sürdürülebilir Kalkınma

Diagnostic Yield of Neuroimaging and Electroencephalography in Children with Recurrent Headaches

ÖZTÜRK HİŞMİ B., TEBER S., Ozkan M., Unal O., Deda G.

JOURNAL OF PEDIATRIC NEUROLOGY , cilt.19, sa.02, ss.76-82, 2021 (ESCI)

A cytology negative rare tumor with the presentation of pseudotumor cerebri clinical symptoms: diffuse leptomeningeal glioneuronal tumor

Yuksel M. F., BEKTAŞ Ö., FİTOZ Ö. S., Goktas O. A., Sahin S., TEBER S.

IRANIAN JOURNAL OF PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.11, sa.2, ss.142-147, 2021 (ESCI)

Febril Konvülziyon Hakkında Hasta Yakınlarının Bilgi, Kaygı ve Düşünceleri

ÖZ TUNÇER G., Dilşa Cemre A., ALBAYRAK P., KUTLUK M. G., TEBER S., DEDA G.

Türkiye Çocuk Hastalıkları Dergisi , cilt.15, sa.1, ss.19-23, 2021 (Hakemli Dergi)

Sublingual Atropine Sulfate Use for Sialorrhea in Pediatric Patients

Azapağası E., KENDİRLİ T., Perk O., kutluk g., Öz T. G., TEBER S., et al.

Journal of Pediatric Intensive Care , cilt.9, sa.03, ss.196-200, 2020 (ESCI)

Birincil Baş Ağrısı Olan Çocuk ve Ergenlerde Psikopatoloji ve Annelerinde Artmış Depresyon Düzeyleri: Kontrollü Bir Çalışma

Akçay E., tuncer g. ö., TEBER S., KILIÇ B. G.

Turk J Child Adolesc Ment Health , cilt.27, sa.1, ss.49-55, 2020 (Hakemli Dergi) Sürdürülebilir Kalkınma

A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene

Tuncer G. O., TEBER S., Albayrak P., Kutluk M. G., Deda G.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.53, sa.4, ss.259-262, 2018 (ESCI)

Optik Gliom’da İmatinib Mesilat İlişkili Tedavi Sonuçlarımız:Tek Merkez Deneyimi

TANYILDIZ H. G., TAÇYILDIZ N., DİNÇASLAN H., ÜNAL E., TEBER S., BEKTAŞ Ö., et al.

Türkiye Çocuk Hastalıkları Dergisi , 2018 (Hakemli Dergi)

Limb girdle muscular dsıtophy type 2a associated with hepatic involvement: a case report

Yüksel M., Bektaş Ö., EMİNOĞLU F. T., KULOĞLU Z., TEBER S.

Acta Myologiaca , cilt.37, ss.160, 2018 (Scopus)

İnme ve Serebrovasküler Hastalıklar

BEKTAŞ Ö., TEBER S., DEDA G.

Turkiye Klinikleri J Pediatr Sci , cilt.14, sa.1, ss.148-163, 2018 (Hakemli Dergi)

Cutaneous Ulceration Associated with Subcutaneous Interferon Beta 1a Injection

ÖZ T. G., ALBAYRAK P., KUTLUK M. G., AKINCI G. Ö., TEBER S.

Turkish Journal of Pediatric Disease , 2018 (Hakemli Dergi)

The Electroencephalogram in Learning Disability: Special Emphasis on Interictal Epileptiform Discharges

ARHAN E., GÜNEY E., Bulan A., Karalok S., TEBER S., Guven A., et al.

GAZI MEDICAL JOURNAL , cilt.28, sa.3, ss.171-173, 2017 (ESCI)

Andersen-Tawil Syndrome with Early Onset Myopathy: 2 Cases

Oz Tuncer G., TEBER S., Kutluk M. G., Albayrak P., Deda G.

Journal of Neuromuscular Diseases , cilt.4, sa.1, ss.93-95, 2017 (Scopus)

Çocukluk Çağı Migreninde Profilaktik Tedavinin Değerlendirilmesi

YILMAZ A., BEKTAŞ Ö., TEBER S., DEDA G.

Ankara Eğitim ve Araştırma Hastanesi Tıp Dergisi , cilt.49, sa.2, ss.107-113, 2016 (Hakemli Dergi)

Late Presentation of Ataxia, Areflexia, and Electrophysiological Abnormalities as Part of Miller Fisher Syndrome: Case Report

Somer D., Yilmaz A., TEBER S., Cinar F. G.

NEURO-OPHTHALMOLOGY , cilt.40, sa.4, ss.197-200, 2016 (ESCI)

Marcus Gunn Jaw Winking Sinkinezis Konjenital Pitozisli İkiOlgunun Sunumu

BEKTAŞ Ö., KORKMAZ V., TEBER S., DEMİR A. M., KULOĞLU Z., KANSU A., et al.

Türkiye Çocuk Hastalıkları Dergisi , cilt.9, sa.3, ss.203-205, 2015 (Hakemli Dergi)

Megalensefalik Lökoensefalopati ile Subkortikal Kistler veMakrosefali Olgu Sunumu

BEKTAŞ Ö., KORKMAZ V., TEBER S., DEMİR A. M., KULOĞLU Z., KANSU A., et al.

Türkiye Çocuk Hastalıkları Dergisi , cilt.9, sa.2, ss.134-136, 2015 (Hakemli Dergi)

Akçaağaç Şurubu İdrar Hastalığı Ensefalopatisinde MR veDifüzyon MR Görüntüleri

BEKTAŞ Ö., KORKMAZ V., TEBER S., DEMİR A. M., KULOĞLU Z., KANSU A., et al.

Türkiye Çocuk Hastalıkları Dergisi , cilt.9, sa.1, ss.59-61, 2015 (Hakemli Dergi)

Nöröfi bromatozis Tip 1 ve Epilepsili Hastaların KlinikKarakteristikleri

BEKTAŞ Ö., KORKMAZ V., TEBER S., DEMİR A. M., KULOĞLU Z., KANSU A., et al.

Türkiye Çocuk Hastalıkları Dergisi , cilt.8, sa.3, ss.137-140, 2014 (Hakemli Dergi)

Canavan Disease Mri and Mrs Findings: 3 Different Cases

AKMAZ ÜNLÜ H., ALTINBAŞ N. K., TEBER S., DERİNKUYU B. E., ÜNLÜ S. E., GÜLEROĞLU N. B., et al.

Turkish Journal of Pediatric Disease , cilt.7, sa.4, ss.201-205, 2013 (Hakemli Dergi)

Pseudotumor cerebri associated with cod liver oil use: Case report

BEKTAŞ Ö., Yilmaz A., TEBER S., Aksoy E., Deda G.

Turkiye Klinikleri Pediatri , cilt.22, sa.3, ss.143-145, 2013 (Scopus)

A type of progressive myoclonic epilepsy, Lafora disease: A case report

BEKTAŞ Ö., Yilmaz A., Heper Okcu A., Teber S., Aksoy E., Deda G.

Eastern Journal of Medicine , cilt.18, sa.1, ss.34-36, 2013 (Scopus)

Subacute sclerosing panencephalitis with an atypical presentation: A case report

TEBER S., Sezer T., Kafali M., Deda G.

Journal of Pediatric Neurology , cilt.9, sa.1, ss.127-130, 2011 (Scopus)

Treatment challenges in pediatric stroke patients

YILMAZ A., Teber S., BEKTAŞ Ö., Akar N., Uysal L., AKSOY E. İ., et al.

Stroke Research and Treatment , cilt.2011, 2011 (ESCI)

Atypical clinical and neuroradiological presentation in a patient with mitochondrial neurogastrointestinal encephalomyopathy with anterior leukoencephalopathy

TEBER S., Yilmaz A., Teber M. A., BEKTAŞ Ö., Aksoy E., Deda G.

Eastern Journal of Medicine , cilt.15, sa.3, ss.103-107, 2010 (Scopus)

Encephalitis in Children: Presentation of 27 Cases

ÖZDEMİR H., TAPISIZ A., Çiftçi E., İNCE E., KENDİRLİ T., FİTOZ Ö. S., et al.

JOURNAL OF PEDIATRIC INFECTION , sa.4, ss.168-173, 2009 (ESCI)

Prothrombotic risk factors in childhood migraine and comparison of acetylsalicyclic acid and propranolol in prophylactic therapy

TEBER S., Uysal Z., Akar N., Deda G.

Journal of Pediatric Neurology , cilt.5, sa.2, ss.121-126, 2007 (Scopus)

Behçet's disease as cause of sinovenous thrombosis in a pediatric patient

TEBER S., Unal O., Deda G., FİTOZ Ö. S., Uysal Z., Akar N.

Journal of Pediatric Neurology , cilt.4, sa.2, ss.139-142, 2006 (Scopus)

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