Metrics
Publication
75
Open Access
3
UN Sustainable Development Goals
Education
2014 - 2017
2014 - 2017Post Doctorate of Medicine
Istanbul University, Istanbul Medical Faculty, Çocuk Nörolojisi, Turkey
2006 - 2012
2006 - 2012Expertise In Medicine
Istanbul University, Instıtute of Chıld Health, Dahili Tıp Bilimleri Bölümü, Turkey
1999 - 2005
1999 - 2005Associate Degree
Istanbul University, Istanbul Medical Faculty, Turkey
Dissertations
2011
2011Expertise 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
Academic Positions
2019 - Present
2019 - PresentAssociate Professor
Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences
Non Academic Experience
2017 - Present
2017 - PresentÇOCUK NÖROLOJİSİ UZMANI
İSTANBUL KANUNİ SULTAN SÜLEYMAN EĞİTİM VE ARAŞTIRMA HASTANESİ, ÇOCUK NÖROLOJİSİ UZMANI
2017 - 2019
2017 - 2019Other Public Institution, Kanuni Sultan Süleyman Eğitim Ve Araştırma Hastanesi
2012 - 2013
2012 - 2013ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI
KIZILTEPE DEVLET HASTANESİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI KLİNİĞİ, ÇOCUK SAĞLIĞI VE HASTALIKLARI UZMANI
Articles
All (43)
SCI-E, SSCI, AHCI (38)
SCI-E, SSCI, AHCI, ESCI (41)
ESCI (3)
Scopus (41)
TRDizin (7)
2025
20251. 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
20252. 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
20253. 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)
2024
20244. 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
20245. 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)
2024
20246. 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)
2024
20247. 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)
2023
20238. 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
20229. 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
202210. 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
202211. 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
202212. 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
202213. 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
202214. 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
202115. 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)
2021
202116. 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
202117. 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)
2021
202118. 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
202019. 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
202020. 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
201921. 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
201922. 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
201923. 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
201924. 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
201925. 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
201826. 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
201827. 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)
2018
201828. 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
201829. 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
201730. 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
201731. 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
201732. 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
201733. 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
201734. 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
201735. 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
201736. 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
201737. 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
201638. 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
201639. 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)
2015
201540. 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
201541. 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
201442. 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
201243. 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
20251. 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
20252. 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
20243. 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
20244. 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
20235. 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
20236. 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
20227. 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
20228. 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
20219. Otoimmünite ve Epilepsi
PEMPEGÜL YILDIZ E.
23. ULUSAL ÇOCUK NÖROLOJİSİ KONGRESİ, İzmir, Turkey, 27 October 2021, (Summary Text)
2021
202110. 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
202111. 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
202112. 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
201913. 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
201714. 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
201515. 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
201416. 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
20241. 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
20232. "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
20233. Makrofaj Aktivasyon Sendromları
Avcı R., PEMPEGÜL YILDIZ E.
in: Nöroimmünoloji, Mehmet Canpolat, Editor, Türkiye Klinikleri Pediatri Dergisi, İstanbul, pp.254-259, 2023
2023
20234. 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
20235. 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
20236. 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
20237. 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
20228. 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
20219. Ataksi
Pempegül Yıldız E., Çalışkan M. M.
in: Çocuklarda Bulgudan Tanıya Algoritmalar, Ergun Çil, Editor, İstanbul Medikal Yayıncılık, İstanbul, pp.49-53, 2021
2021
202110. 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
202111. 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
202112. Ataksi
PEMPEGÜL YILDIZ E., ÇALIŞKAN M. M.
in: Çocuklarda Bulgudan Tanıya Algoritmalar, Ergün Çil, Editor, İstanbul Medikal Yayıncılık, İstanbul, pp.49-53, 2021
2020
202013. 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
202014. 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
202015. 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
Funded Projects
2022 - 2024
2022 - 2024Lizozomal Depo Hastalıklarında Enzimatik Tanı Yöntemlerinin Kurulması Optimizasyonu ve Validasyonu
Project Supported by Higher Education Institutions , BAP Research Project
GEDİKBAŞI A. (Executive), AYDOĞDU P., GÖKÇAY G. F., AYDIN A. F., BALCI M. C., KARACA M., et al.
Peer Reviews in Scientific Publications
December 2021
December 2021ACTA NEUROLOGICA BELGICA
SCI Journal
July 2021
July 2021ÇOCUK DERGİSİ
National Scientific Refreed Journal
December 2020
December 2020ÇOCUK DERGİSİ
National Scientific Refreed Journal
December 2020
December 2020İSTANBUL TIP FAKÜLTESİ DERGİSİ
National Scientific Refreed Journal
October 2020
October 2020ÇOCUK DERGİSİ
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August 2020
August 2020TÜRK PEDİATRİ ARŞİVİ
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March 2020
March 2020İSTANBUL TIP DERGİSİ
National Scientific Refreed Journal