Prof. EDİBE PEMPEGÜL YILDIZ

Metrics

Publication

Publication (WoS)

Publication (Scopus)

Citation (WoS)

404

H-Index (WoS)

Citation (Scopus)

474

H-Index (Scopus)

Citation (Scholar)

H-Index (Scholar)

Project

Thesis Advisory

Open Access

UN Sustainable Development Goals

Education

2014 - 2017

Post Doctorate of Medicine

Istanbul University, Istanbul Medical Faculty, Çocuk Nörolojisi, Turkey

2006 - 2012

Expertise In Medicine

Istanbul University, Instıtute of Chıld Health, Dahili Tıp Bilimleri Bölümü, Turkey

1999 - 2005

Associate Degree

Istanbul University, Istanbul Medical Faculty, Turkey

Dissertations

2011

Expertise In Medicine

Yenidoğan konvülziyonlarıetiyolojik ve prognositik faktörlerin değerlendirilmesi

Istanbul University, Instıtute of Chıld Health, Dahili Tıp Bilimleri Bölümü

Research Areas

Medicine

Health Sciences

Internal Medicine Sciences

Child Health and Diseases

Pediatric Neurology

Research Areas Based on Academic Activities

Avesis Research Areas

WoS Research Areas

Scopus Research Areas

Academic Positions

2019 - Present

Associate Professor

Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences

Non Academic Experience

2017 - Present

ÇOCUK NÖROLOJİSİ UZMANI

İSTANBUL KANUNİ SULTAN SÜLEYMAN EĞİTİM VE ARAŞTIRMA HASTANESİ, ÇOCUK NÖROLOJİSİ UZMANI

2017 - 2019

Other Public Institution, Kanuni Sultan Süleyman Eğitim Ve Araştırma Hastanesi

2012 - 2013

ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI

KIZILTEPE DEVLET HASTANESİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI KLİNİĞİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI

Articles

2025

1. Electrocardiographic Markers of Sudden Unexpected Death Risk in Pediatric Epilepsy: A Comparative Study of Generalized and Focal Seizures

KARACA S., Ozbingol D., KARACA ÖZER P., YAVUZ M. L., NİŞLİ K., ÖZTARHAN K., et al.

DIAGNOSTICS , vol.15, no.13, 2025 (SCI-Expanded)

2025

2. Benchmarking Nanopore Sequencing for CLN2 (TPP1) Mutation Detection: Integrating Rapid Genomics and Orthogonal Validation for Precision Diagnostics

Teker B., Akan G., Kazan H. H., ÖZGEN ÇOBAN Ö., Tatonyan S., BALCI M. C., et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , vol.26, no.11, 2025 (SCI-Expanded, Scopus)

2025

3. Case Report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review

Bayraktar Eltutan C., Rinaldi S., Vural A., Aksu B., Maras Genc H., Pembegul Yildiz E.

Frontiers in Immunology , vol.16, 2025 (SCI-Expanded)

2025

4. Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort

Gülşen M., Dursun O. B., TEKİN A., Yüksel D., DEMİR E., ÖZTÜRK G., et al.

Frontiers in Neurology , vol.16, 2025 (SCI-Expanded, Scopus)

2024

5. Machine learning models for predicting treatment response in infantile epilepsies.

Pembegul Yildiz E., Coskun O., Kurekci F., Maras Genc H., Ozaltin O.

Epilepsy & behavior : E&B , vol.160, pp.110075, 2024 (SCI-Expanded)

2024

6. Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects

Kurekci F., Akif Kilic M. A., Akbas S., Avci R., Oney C., Dilruba Aslanger A., et al.

EPILEPSY & BEHAVIOR , vol.158, 2024 (SCI-Expanded, Scopus)

2024

7. Association of epilepsy with neuroimaging patterns in children with cerebral palsy

Kilic M. A., Yildiz E., Kurekci F., Coskun O., Cura M., Avci R., et al.

ACTA NEUROLOGICA BELGICA , vol.124, no.2, pp.567-572, 2024 (SCI-Expanded, Scopus)

2024

8. A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants

Kilic M. A., Yildiz E., Deniz A., Coskun O., Kurekci F., Avci R., et al.

PEDIATRIC NEUROLOGY , vol.152, pp.189-195, 2024 (SCI-Expanded, Scopus)

2023

9. Genetic and clinical evaluation of congenital myasthenic syndromes with long-term follow-up: experience of a tertiary center in Turkey

Yildiz E., Kilic M. A., Yalcin E. U., Kurekci F., Avci R., Hacifazlioglu N. E., et al.

ACTA NEUROLOGICA BELGICA , vol.123, no.5, pp.1841-1847, 2023 (SCI-Expanded)

2022

10. Seizure treatment with olfactory training: a preliminary trial.

Yilmaz Y., Turk B. G., Ser M. H., Sut N. Y., Sahin S., Yildiz E., et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology , vol.43, no.12, pp.6901-6907, 2022 (SCI-Expanded)

2022

11. Evaluation of inflammatory acquired demyelinating syndromes in children: a single-center experience.

Kılıç H., Mavi D., Yalcinkaya B. C., Yildiz E., Kizilkilic O., Saltık S.

Acta neurologica Belgica , vol.122, no.6, pp.1485-1491, 2022 (SCI-Expanded)

2022

12. Shear Wave Elastography in Patients with Spinal Muscular Atrophy Types 2 and 3

Karacabey B. N., Bayramoglu Z., Coskun O., Sari Z. N. A., Ozkan M. U., PEMPEGÜL YILDIZ E., et al.

NEUROPEDIATRICS , vol.54, no.4, pp.273-278, 2022 (SCI-Expanded)

2022

13. 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 , vol.41, pp.8-18, 2022 (SCI-Expanded)

2022

14. Preliminary validation of the Turkish version of the pain catastrophizing scale for children and parents (PCS-C and PCS-P) in primary childhood headache

Senturk I. A., ÜNAL E., TARAKÇIOĞLU M. C., Kepekci M., Yildiz E.

AGRI-THE JOURNAL OF THE TURKISH SOCIETY OF ALGOLOGY , vol.34, no.4, pp.278-291, 2022 (ESCI)

2022

15. Late onset Aicardi-Goutières syndrome case report: a rare white matter disease mimicking as pseudo-enzyme deficiency.

Ulak Ozkan M., Katar S., Pembegul Yildiz E., Aydinli N., Caliskan M.

Acta neurologica Belgica , vol.122, no.1, pp.259-261, 2022 (SCI-Expanded)

2021

16. Pediatric LGI1 and CASPR2 autoimmunity associated with COVID 19: Morvan syndrome

Kılıç M. A., Yoruk Yildirim Z. N., Oner A., Yeşil E., Aksu B., Pempegül Yıldız E., et al.

JOURNAL OF NEUROLOGY , vol.268, no.12, pp.4492-4494, 2021 (SCI-Expanded, Scopus)

2021

17. Homozygous SQSTM1 nonsense variant identified in a patient with brainstem involvement

Kilic M. A., Kipoglu O., Coskun O., Karacabey B. N., Yesilyurt A., Yildiz E., et al.

BRAIN & DEVELOPMENT , vol.43, no.10, pp.1039-1043, 2021 (SCI-Expanded)

2021

18. Progressive Multifocal Leukoencephalopathy in Children with Primary and Secondary Immune Deficiency.

Demirbuga A., Kaba O., Torun S., Yildiz E., Yucel E., Somer A.

Pediatric allergy, immunology, and pulmonology , vol.34, no.3, pp.109-111, 2021 (SCI-Expanded, Scopus)

2021

19. Evaluation of eating behaviors in childhood epilepsy with centrotemporal spikes: Case-control study.

Coskun O., Kipoglu O., Karacabey B. N., Kilic M. A., Ceran D. S., Yildiz E., et al.

Epilepsy & behavior : E&B , vol.120, pp.108029, 2021 (SCI-Expanded)

2020

20. Evaluation of the prognostic factors in school age children who experienced neonatal seizures.

Yildiz E., Tatli B., Ozkan M. U., Erarslan E., Aydinli N., Caliskan M., et al.

Epilepsy & behavior : E&B , vol.102, pp.106673, 2020 (SCI-Expanded)

2020

21. Clinically isolated syndrome and multiple sclerosis in children: a single center study.

Bektaş G., Özkan M., Yıldız E., Uzunhan T., Sencer S., Aydınlı N., et al.

The Turkish journal of pediatrics , vol.62, pp.244-251, 2020 (SCI-Expanded)

2019

22. Epileptic spasm and other forms of epilepsy in presumed perinatal arterial ischemic stroke in Turkey after more than 10 years follow-up: A single centre study.

BEKTAŞ G., KIPOĞLU O., Pembegül Y., AYDıNLı N., ÇALıŞKAN M., ÖZMEN M., et al.

Brain & development , vol.41, pp.699-705, 2019 (SCI-Expanded)

2019

23. Autism spectrum disorder and attention-deficit/hyperactivity disorder-related symptoms in benign childhood epilepsy with centrotemporal spikes: A prospective case-control study.

BEKTAŞ G., TEKIN U., Yıldız E., AYDıNLı N., ÇALıŞKAN M., ÖZMEN M.

Epilepsy & behavior : E&B , vol.95, pp.61-64, 2019 (SCI-Expanded)

2019

24. Neurological and Psychosocial Evaluation of Pediatric Celiac Patients: Diet Adherence-Case Control Study

Yildiz E., Civan H. A.

MEDICAL JOURNAL OF BAKIRKOY , vol.15, no.1, pp.110-114, 2019 (ESCI)

2019

25. Psychosocial And Behavioral Functioning of Cognitively Normal Children with History of Neonatal Seizure: Case Control Study

Pempegül Yıldız E.

İstanbul Kanuni Sultan Süleyman Tıp Dergisi , vol.11, no.2, pp.70-74, 2019 (Peer-Reviewed Journal)

2019

26. Efficacy of Stiripentol and the Clinical Outcome in Dravet Syndrome.

Yıldız E., Ozkan M., Uzunhan T., Bektaş G., Tatlı B., Aydınlı N., et al.

Journal of child neurology , vol.34, pp.33-37, 2019 (SCI-Expanded)

2018

27. Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up.

Bektas G., Bektas G., YEŞİL G., YEŞİL G., Ozkan M. U., Ozkan M. U., et al.

Clinical neurology and neurosurgery , vol.171, pp.190-193, 2018 (SCI-Expanded)

2018

28. Predictive factors of drug-resistant epilepsy in children presenting under 2 years of age: experience of a tertiary center in Turkey.

Yildiz E., Gunes D., Bektas G., Uzunhan T. A., Tatli B., Caliskan M., et al.

Acta neurologica Belgica , vol.118, no.1, pp.71-75, 2018 (SCI-Expanded, Scopus)

2018

29. Efficacy of rufinamide in childhood refractory epilepsy

Yildiz E., Hizli Z., Bektas G., Ulak-Ozkan M., Tatli B., Aydinli N., et al.

Turkish Journal of Pediatrics , vol.60, no.3, pp.238-243, 2018 (SCI-Expanded)

2018

30. Spinal muscular atrophy with progressive myoclonic epilepsy linked to mutations in ASAH1.

YILDIZ E. P., Yildiz E., YEŞİL G., YEŞİL G., BEKTAS G., Bektas G., et al.

Clinical neurology and neurosurgery , vol.164, pp.47-49, 2018 (SCI-Expanded)

2017

31. Lacosamide treatment of childhood refractory focal epilepsy: the first reported side effect in paediatric patients.

Yildiz E., Ozkan M. U., Bektas G., Uzunhan T. A., Aydinli N., Caliskan M., et al.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery , vol.33, no.11, pp.2023-2027, 2017 (SCI-Expanded)

2017

32. A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.

YILDIZ E., YILDIZ E. P., YEŞİL G., YESIL G., OZKAN M. U., OZKAN M. U., et al.

Seizure , vol.51, pp.77-79, 2017 (SCI-Expanded)

2017

33. The influence of levetiracetam on psychosocial and behavioral functioning in children: A case-control and follow-up study.

Bektaş G., TEKIN U., ÖZKAN M. U., YıLDıZ E., ÇALıŞKAN M., ÖZMEN M., et al.

Epilepsy & behavior : E&B , vol.72, pp.39-42, 2017 (SCI-Expanded)

2017

34. Potential risk factors for vitamin D levels in medium- and long-term use of antiepileptic drugs in childhood.

YILDIZ E., POYRAZOGLU Ş., Bektas G., KARDELEN A. D., AYDıNLı N.

Acta neurologica Belgica , vol.117, pp.447-453, 2017 (SCI-Expanded)

2017

35. Psychosocial and behavioral functioning and their relationship to seizure timing in children with benign epilepsy with centrotemporal spikes.

Bektaş G., TEKIN U., Yıldız E., UZUNHAN T. A., TATLI B., AYDıNLı N., et al.

Brain & development , vol.39, pp.515-520, 2017 (SCI-Expanded)

2017

36. Neonatal hypoxic ischemic encephalopathy: an update on disease pathogenesis and treatment.

Yildiz E., Ekici B., Tatli B.

Expert review of neurotherapeutics , vol.17, no.5, pp.449-459, 2017 (SCI-Expanded)

2017

37. Coexisting neuronal autoantibodies among children with demyelinating syndromes.

Kiztanir H., Bektas G., Yildiz E., Uzunhan T. A., Tatli B., Aydinli N., et al.

Brain & development , vol.39, no.3, pp.248-251, 2017 (SCI-Expanded)

2017

38. Hereditary spastic paraplegia type 35 caused by a novel FA2H mutation.

Bektas G., Bektas G., Yesil G., YEŞİL G., Yildiz E., Yildiz E. P., et al.

The Turkish journal of pediatrics , vol.59, no.3, pp.329-334, 2017 (SCI-Expanded)

2016

39. Aggravation of atonic seizures by rufinamide: A case report.

Bektas G., Caliskan M., Aydin A., Yildiz E., Tatli B., Aydinli N., et al.

Brain & development , vol.38, no.7, pp.654-7, 2016 (SCI-Expanded)

2016

40. Role of Autoantibodies to N-Methyl-d-Aspartate (NMDA) Receptor in Relapsing Herpes Simplex Encephalitis: A Retrospective, One-Center Experience.

SUTCU M., AKTURK H., SOMER A., TATLI B., Torun S., YıLDıZ E., et al.

Journal of child neurology , vol.31, pp.345-50, 2016 (SCI-Expanded, Scopus)

2015

41. Çocukluk Çağında Guillain-Barré Sendromu

VARKAL M. A., PEMPEGÜL YILDIZ E., YILDIZ İ., AYDINLI N., ÜNÜVAR E.

Çocuk Dergisi , vol.15, pp.89-98, 2015 (Peer-Reviewed Journal)

2015

42. Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis.

Pehlivan D., Akdemir Z. C., Karaca E., Bayram Y., Jhangiani S., Yildiz E., et al.

Human genetics , vol.134, no.6, pp.671-3, 2015 (SCI-Expanded)

2014

43. A classical phenotype of Duchenne muscular dystrophy in a girl with X; autosome translocation.

UZUNHAN T., Altunoğlu U., YıLDıZ E., AYDıNLı N.

Journal of pediatric neurosciences , vol.9, pp.290-1, 2014 (ESCI)

2012

44. Evaluation of etiologic and prognostic factors in neonatal convulsions.

Yildiz E., Tatli B., Ekici B., Eraslan E., Aydinli N., Caliskan M., et al.

Pediatric neurology , vol.47, no.3, pp.186-92, 2012 (SCI-Expanded)

Papers Presented at Peer-Reviewed Scientific Conferences

2025

1. Etiology and prognosis of developmental and epileptic encephalopathies: genotype-phenotype correlation

Kürekçi F., Maraş Genç H., Aslanger A., Pempegül Yıldız E.

EPNS 2025, Munich, Germany, 10 July 2025, (Full Text)

2025

2. Friedreich ataxia and impaired steroidogenesis

Bayrak Demirel Ö., Öney C., Akbaş S., Kandemir T., Aslanger A. D., Kardelen Al A. D., et al.

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course, Kobenhavn, Denmark, 10 - 13 May 2025, pp.185-186, (Summary Text)

2024

3. Pharyngeal-cervical-brachial variant of Guillain Barré syndrome with anti ganglioside antibodies

Orazova M., Pempegül Yıldız E., Duru Can E. C., Maraş Genç H., Abbasalıyev V.

European Paediatric Association's Congress , Antalya, Turkey, 17 - 21 April 2024, vol.1, pp.84-85, (Full Text)

2024

4. The complexity of Phelan-McDermid syndrome: A multifaceted exploration of clinical and molecular/cytogenetic findings in four cases.

Yücesoy M. A., Akbaş S., Memiş G., Konur Akbaş E. N., Durmaz D., Karaman V., et al.

European Society of Genetics Conference 2024, Berlin, Germany, 1 - 04 June 2024, (Summary Text)

2023

5. Mitokondriyal hastalıklarda nörogörüntüleme: alışılmadık tutulumların nadir genetik nedenleri

PEMPEGÜL YILDIZ E., KÜREKCİ F., BALCI M. C., KARACA M., MARAŞ GENÇ H., GÖKÇAY G. F.

Ulusal Çocuk Nörolojisi Kongresi, Muğla, Turkey, 17 - 21 May 2023, pp.147-148, (Full Text)

2023

6. Fluorometric Analysis and Validation of Tripeptidyl Peptidase-1 in Dry Blood Samples and Leukocytes in the Diagnosis of Neuronal Ceroid Lipofuxinosis 2

Teker B., Tatonyan S., Gedikbaşı A., Aydın A. F., Balcı M. C., Karaca M., et al.

VIII. Uluslararası Katılımlı Lizozomal Hastalıklar Kongresi, Bursa, Turkey, 3 - 07 May 2023, pp.64, (Summary Text)

2022

7. ASSOCIATION OF NF-1 AND MOYAMOYA SYNDROME : CASE REPORT

KARAMAN S., Şahin Ş., PEMPEGÜL YILDIZ E., TANYILDIZ H. G., BARBUROĞLU M., TURGUT G. T., et al.

XIII Eurasian Hematology-Oncology Congress (EHOC 2022), İstanbul, Turkey, 05 October 2022, vol.44, pp.69-70, (Summary Text)

2022

8. Retrospective Evaluation of Our Cases Diagnosed with Thiamine Biotin-Sensitive Basal Ganglion Disease

Körbeyli H. K., Kılıç M. A., Balcı M. C., Pempegül Yıldız E., Gökçay G. F.

44. PEDİATRİ GÜNLERİ 23. PEDİATRİ HEMŞİRELİĞİ GÜNLERİ, İstanbul, Turkey, 17 - 20 April 2022, pp.85, (Summary Text)

2021

9. Otoimmünite ve Epilepsi

PEMPEGÜL YILDIZ E.

23. ULUSAL ÇOCUK NÖROLOJİSİ KONGRESİ, İzmir, Turkey, 27 October 2021, (Summary Text)

2021

10. Unilateral Propitozla Başvuran Nöro-Behçet Olgusu

Demirkan F. G., Akgün Ö., Kavrul Kayaalp G., Çakmak F., Kılıç M. A., Pempegül Yıldız E., et al.

43.Pediatri Günleri, İstanbul, Turkey, 30 May - 02 June 2021, pp.331, (Summary Text)

2021

11. Nadir Görülen Bir Epileptik Ensefalopati: Erken İnfantil Epileptik Ensefalopati Tip 22

Tırtır Yılmaz B., Kılıç M. A., Pempegül Yıldız E.

43.Pediatri Günleri 22.Pediatri Hemşireliği Günleri, 30 May - 02 June 2021, (Unpublished)

2021

12. Hemolitik aneminin nadir bir nedeni: İki olgu ile triozfosfat izomeraz eksikliği

Selamioğlu A., Karaca M., Balcı M. C., Gökçay G. F., Durmuş A., Pempegül Yıldız E., et al.

43. Pediatri Günleri ve 22. Pediatri Hemşireliği Günleri Toplantısı, İstanbul, Turkey, 30 May - 02 June 2021, pp.161, (Full Text)

2019

13. Novel FGFR2 variant in a Case with Crouzon Syndrome

Karaman V., Kalaycı T., Başaran S., Pempegül Yıldız E., Altunoğlu U., Uyguner Z. O.

Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.209, (Summary Text)

2017

14. Sütçocukluğu döneminde ilaca dirençli epilepsi gelişiminde risk faktörleri: Tek merkez deneyimi.

PEMPEGÜL YILDIZ E., GÜNEŞ D., BEKTAŞ G., AKSU UZUNHAN T., TATLI B., ÇALIŞKAN M. M., et al.

39.Pediatri Günleri ve 18. Pediatri Hemşireliği Günleri, İstanbul, Turkey, 2 - 05 April 2017, pp.23, (Summary Text)

2015

15. İNTESTİNAL LENFANJİEKTAZİ TANILI OLGUDA SEMPTOMATİK B12 YETERSİZLİĞİ

YILMAZ Y., PEMPEGÜL YILDIZ E., NİŞLİ K., TATLI B., AYDINLI N., ÇALIŞKAN M. M., et al.

37. PEDİATRİ GÜNLERİ VE 16. PEDİATRİ HEMŞİRELİĞİ GÜNLERİ, 08 April 2015, pp.198, (Summary Text)

2014

16. bir üniversite hastanesinde altı ay içinde yatan herpes virüs ensefalitli olguların değerlendirilmesi

SÜTÇÜ M., HANÇERLİ TÖRÜN S., AKTÜRK H., güntülü ş., PEMPEGÜL YILDIZ E., SOMER A., et al.

58.Türkiye miil pediaytri kongresi, Turkey, 22 - 26 October 2014

Books

2024

1. Yenidoğanda Status Epileptikus

KARACABEY B. N., PEMPEGÜL YILDIZ E.

in: TEMEL PEDIATRIK EPILEPSI, CANPOLAT MEHMET, Editor, Akademisyen Kitabevi A.Ş., İstanbul, pp.667-674, 2024

2023

2. "Çapa Çocuk" Sabah Vaka Arşivleri-I

Balcı M. C., Karaca M., Pempegül Yıldız E., Demirkol D., Gökçay G. F.

in: "Çapa Çocuk" Sabah Vaka Arşivleri-I , Asuman Çoban,Demet Demirkol,Alev Yılmaz,Nuray Aktay Ayaz, Editor, Nobel Tıp Kitapevi, Ankara, pp.31-37, 2023

2023

3. Makrofaj Aktivasyon Sendromları

Avcı R., PEMPEGÜL YILDIZ E.

in: Nöroimmünoloji, Mehmet Canpolat, Editor, Türkiye Klinikleri Pediatri Dergisi, İstanbul, pp.254-259, 2023

2023

4. Nörolojik Hastalıkların Romatolojik Ayırıcı Tanıları

Kürekçi F., PEMPEGÜL YILDIZ E.

in: Çocukluk Çağında Romatizmal Hastalıkların Romatizma Dışı Ayırıcı Tanıları, Prof. Dr. NURAY AKTAY AYAZ, Editor, Türkiye Klinikleri, İstanbul, pp.33-38, 2023

2023

5. Vaka 5

BALCI M. C., KARACA M., PEMPEGÜL YILDIZ E., DEMİRKOL D., GÖKÇAY G. F.

in: Çapa Çocuk Sabah Vaka Arşivleri I, Çoban Asuman, Demirkol D, Yılmaz A, Ayaz Aktay N, Editor, Ankara Nobel Tıp Kitapevi, pp.31-38, 2023

2023

6. Vaka 14

KAHRAMAN H., KÜREKCİ F., PEMPEGÜL YILDIZ E., DEMİRKOL D.

in: Çapa Çocuk Sabah Vaka Arşivleri I, Çoban Asuman, Demirkol D, Yılmaz A, Ayaz Aktay N, Editor, Ankara Nobel Tıp Kitapevi, pp.103-116, 2023

2023

7. Ohtahara Sendromu Tanı ve Tedavı Algoritması

Kılıç M. A., PEMPEGÜL YILDIZ E.

in: Temel Pediatrik Nöroloji: Tanı ve Tedavi, Mehmet Canpolat, Sefer Kumandaş, Editor, Akademisyen Kitapevi, İstanbul, pp.579-583, 2023

2022

8. Çocuklarda immünomodülatör tedavi ve IVIG uygulamaları

PEMPEGÜL YILDIZ E., ÇALIŞKAN M. M.

in: Pediatrik Nöroloji: Algoritmalar ve İlaç Rehberi, Mehmet Canpolat, Sefer Kumandaş, Editor, Akademisyen Kitapevi, İstanbul, pp.3513-3527, 2022

2021

9. Ataksi

Pempegül Yıldız E., Çalışkan M. M.

in: Çocuklarda Bulgudan Tanıya Algoritmalar, Ergun Çil, Editor, İstanbul Medikal Yayıncılık, İstanbul, pp.49-53, 2021

2021

10. Çocuk Nörolojisi Bilim Dalı Bakış Açısıyla Covid-19

Pempegül Yıldız E., Karacabey B. N., Çalışkan M. M., Aydınlı N.

in: Çocuklarda HEr Yönüyle Covid-19, Zeynep Karakaş,Demet Demirkol,Burçin Nazlı Karacabey, Editor, Selen Yayıncılık, İstanbul, pp.209-218, 2021

2021

11. Çocuk Nörolojisi Bilim Dalı Bakış Açısıyla Covid-19

KARACABEY B. N., PEMPEGÜL YILDIZ E., AYDINLI N., ÇALIŞKAN M. M.

in: Çocuklarda Her Yönüyle Covid-19, Zeynep Karakaş,Demet Demirkol,Burçin Nazlı Karacabey, Editor, Selen Yayıncılık, İstanbul, pp.209-218, 2021

2021

12. Ataksi

PEMPEGÜL YILDIZ E., ÇALIŞKAN M. M.

in: Çocuklarda Bulgudan Tanıya Algoritmalar, Ergün Çil, Editor, İstanbul Medikal Yayıncılık, İstanbul, pp.49-53, 2021

2020

13. Sinir ve Kas Sistemi Hastalıkları- Epilepsi Dışı Paroksismal Olaylar

PEMPEGÜL YILDIZ E., AYDINLI N.

in: Pediyatri, Olcay Neyzi, Türkan Ertuğrul, Feyza Darendeliler, Editor, Nobel Tıp Kitabevleri, İstanbul, pp.2049-2053, 2020

2020

14. Sinir ve Kas Sistemi Hastalıkları- Febril Konvilsiyonlar

AYDINLI N., PEMPEGÜL YILDIZ E.

in: Pediyatri, Olcay Neyzi, Türkan Ertuğrul, Feyza Darendeliler, Editor, Nobel Tıp Kitabevleri, İstanbul, pp.2047-2049, 2020

2020

15. Sinir ve Kas Sistemi Hastalıkları- Statik Ensefalopatiler

PEMPEGÜL YILDIZ E., ÖZMEN M.

in: Pediyatri, Olcay Neyzi, Türkan Ertuğrul, Feyza Darendeliler, Editor, Nobel Tıp Kitabevleri, İstanbul, pp.2101-2105, 2020

2019

16. Pediatrik Epileptoloji

Pempegül Yıldız E.

Nobel Tıp Kitapevi, İstanbul, 2019

Funded Projects

2022 - 2024

Prof. EDİBE PEMPEGÜL YILDIZ

Istanbul Medical Faculty, Division of Medical Sciences

Çocuk Nörolojisi Bilim Dalı

WoS Research Areas: Clinical Medicine (Med), Clinical Medicine, Pediatrics

Scopus Research Areas: Pediatrics, Perinatology and Child Health

Avesis Research Areas: Medicine, Health Sciences, Internal Medicine Sciences, Child Health and Diseases, Pediatric Neurology

Metrics

Publication

Publication (WoS)

Publication (Scopus)

Citation (WoS)

H-Index (WoS)

Citation (Scopus)

H-Index (Scopus)

Citation (Scholar)

H-Index (Scholar)

Project

Thesis Advisory

Open Access

Education

Post Doctorate of Medicine

Istanbul University, Istanbul Medical Faculty, Çocuk Nörolojisi, Turkey

Expertise In Medicine

Istanbul University, Instıtute of Chıld Health, Dahili Tıp Bilimleri Bölümü, Turkey

Associate Degree

Istanbul University, Istanbul Medical Faculty, Turkey

Dissertations

Expertise In Medicine

Yenidoğan konvülziyonlarıetiyolojik ve prognositik faktörlerin değerlendirilmesi

Istanbul University, Instıtute of Chıld Health, Dahili Tıp Bilimleri Bölümü

Research Areas

Medicine

Health Sciences

Internal Medicine Sciences

Child Health and Diseases

Pediatric Neurology

Research Areas Based on Academic Activities

Avesis Research Areas

WoS Research Areas

Scopus Research Areas

Academic Positions

Associate Professor

Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences

Non Academic Experience

ÇOCUK NÖROLOJİSİ UZMANI

İSTANBUL KANUNİ SULTAN SÜLEYMAN EĞİTİM VE ARAŞTIRMA HASTANESİ, ÇOCUK NÖROLOJİSİ UZMANI

Other Public Institution, Kanuni Sultan Süleyman Eğitim Ve Araştırma Hastanesi

ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI

KIZILTEPE DEVLET HASTANESİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI KLİNİĞİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI

Articles

1. Electrocardiographic Markers of Sudden Unexpected Death Risk in Pediatric Epilepsy: A Comparative Study of Generalized and Focal Seizures

KARACA S., Ozbingol D., KARACA ÖZER P., YAVUZ M. L., NİŞLİ K., ÖZTARHAN K., et al.

DIAGNOSTICS , vol.15, no.13, 2025 (SCI-Expanded)

2. Benchmarking Nanopore Sequencing for CLN2 (TPP1) Mutation Detection: Integrating Rapid Genomics and Orthogonal Validation for Precision Diagnostics

Teker B., Akan G., Kazan H. H., ÖZGEN ÇOBAN Ö., Tatonyan S., BALCI M. C., et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , vol.26, no.11, 2025 (SCI-Expanded, Scopus)

3. Case Report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review

Bayraktar Eltutan C., Rinaldi S., Vural A., Aksu B., Maras Genc H., Pembegul Yildiz E.

Frontiers in Immunology , vol.16, 2025 (SCI-Expanded)

4. Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort

Gülşen M., Dursun O. B., TEKİN A., Yüksel D., DEMİR E., ÖZTÜRK G., et al.

Frontiers in Neurology , vol.16, 2025 (SCI-Expanded, Scopus)

5. Machine learning models for predicting treatment response in infantile epilepsies.

Pembegul Yildiz E., Coskun O., Kurekci F., Maras Genc H., Ozaltin O.

Epilepsy & behavior : E&B , vol.160, pp.110075, 2024 (SCI-Expanded)

6. Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects

Kurekci F., Akif Kilic M. A., Akbas S., Avci R., Oney C., Dilruba Aslanger A., et al.

EPILEPSY & BEHAVIOR , vol.158, 2024 (SCI-Expanded, Scopus)

7. Association of epilepsy with neuroimaging patterns in children with cerebral palsy

Kilic M. A., Yildiz E., Kurekci F., Coskun O., Cura M., Avci R., et al.

ACTA NEUROLOGICA BELGICA , vol.124, no.2, pp.567-572, 2024 (SCI-Expanded, Scopus)

8. A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants

Kilic M. A., Yildiz E., Deniz A., Coskun O., Kurekci F., Avci R., et al.

PEDIATRIC NEUROLOGY , vol.152, pp.189-195, 2024 (SCI-Expanded, Scopus)

9. Genetic and clinical evaluation of congenital myasthenic syndromes with long-term follow-up: experience of a tertiary center in Turkey

Yildiz E., Kilic M. A., Yalcin E. U., Kurekci F., Avci R., Hacifazlioglu N. E., et al.

ACTA NEUROLOGICA BELGICA , vol.123, no.5, pp.1841-1847, 2023 (SCI-Expanded)

10. Seizure treatment with olfactory training: a preliminary trial.

Yilmaz Y., Turk B. G., Ser M. H., Sut N. Y., Sahin S., Yildiz E., et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology , vol.43, no.12, pp.6901-6907, 2022 (SCI-Expanded)

4. Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort

Epilepsy & behavior : E&B , vol.102, pp.106673, 2020 (SCI-Expanded)

22. Epileptic spasm and other forms of epilepsy in presumed perinatal arterial ischemic stroke in Turkey after more than 10 years follow-up: A single centre study.

Brain & development , vol.41, pp.699-705, 2019 (SCI-Expanded)

Epilepsy & behavior : E&B , vol.95, pp.61-64, 2019 (SCI-Expanded)