Yayınlar & Eserler

Yayın Ağı
Makaleler 34
Tümü (34)
SCI-E, SSCI, AHCI (28)
SCI-E, SSCI, AHCI, ESCI (31)
ESCI (2)
Scopus (34)
TRDizin (8)

1. Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohort

Üstün C., Polat İ., ÖZTÜRK G., ÜNVER O., TÜRKDOĞAN D., Kanmaz S., et al.
Neuromuscular Disorders , cilt.67, 2026 (SCI-Expanded, Scopus)

2. Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping Genetic Findings for McArdle Disease and Dystrophinopathy

Sayar E., KILIÇ M. K., İcil S., Saka-Ümit P., YÜKSEL D., Sezer A., et al.
Klinische Padiatrie , cilt.238, sa.5, ss.288-291, 2026 (SCI-Expanded, Scopus)

3. Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey

Komur M., Çağlar E., Akbeyaz İ. H., Keçebaş A., Yıldız E. P., SALTIK S., et al.
European Journal of Paediatric Neurology , cilt.64, ss.56-64, 2026 (SCI-Expanded, Scopus)

4. Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome

Kanmaz S., Yılmaz S., Dündar N. O., Aksoy A., CANPOLAT M., PER H., et al.
Journal of Child Neurology , cilt.40, sa.10, ss.838-851, 2025 (SCI-Expanded, Scopus)

5. 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 , cilt.16, 2025 (SCI-Expanded, Scopus)

6. Optic neuritis in Turkish children and adolescents: A multicenter retrospective study

Direk M. Ç., Besen Ş., Öncel İ., GÜNBEY C., Özdoğan O., TEKİN ORGUN L., et al.
Multiple Sclerosis and Related Disorders , cilt.81, 2024 (SCI-Expanded, Scopus)

7. Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study

SARIKAYA UZAN G., Vural A., YÜKSEL D., Aksoy E., Öztoprak Ü., CANPOLAT M., et al.
Pediatric Neurology , cilt.145, ss.3-10, 2023 (SCI-Expanded, Scopus)

8. Use of Complementary and Alternative Medicine Practices in Patients Admitted to the Pediatric Neurology Outpatient Clinic Pediatrik Nöroloji Polikliniğine Başvuran Hastalarda Tamamlayıcı ve Alternatif Tıp Uygulamalarının Kullanımı

CEYLAN N., Celik H., ÖZDEMİR M., Aksoy E., Oztoprak U., Atasoy E., et al.
Genel Tip Dergisi , cilt.33, sa.3, ss.242-248, 2023 (Scopus, TRDizin)

9. Characteristics and clinical value of early electroencephalography (EEG) after a first unprovoked seizure in children

Özdemir F. M. A., Öztoprak Ü., Atasoy E., Aksoy E., Çelik H., CEYLAN N., et al.
Neurophysiologie Clinique , cilt.53, sa.1, 2023 (SCI-Expanded, Scopus)

10. Aspects of autism spectrum disorder and correlation with neuroimaging findings in tuberous sclerosis complex

Dedeoğlu Ö., Çetinkaya M., Emine Derinkuyu B., Aksoy E., Öztoprak Ü., Genç Sel Ç., et al.
Clinical Neurology and Neurosurgery , cilt.224, 2023 (SCI-Expanded, Scopus)

11. Evaluation of risk factors, functionalities, and quality of life in patients with pediatric acute arterial ischemic stroke

Özdemir F. M. A., Öztoprak Ü., FETTAH A., ÖRÜN U. A., KILIÇ M. K., Sarıkaya F. G., et al.
Turkish Journal of Pediatrics , cilt.65, sa.2, ss.309-320, 2023 (SCI-Expanded, Scopus, TRDizin)

12. Evaluation of clinical and electroencephalographic findings in patients with early childhood epilepsy and inborn errors of metabolism

Celik H., Ozdemir F. M. A., Aksoy E., Oztoprak U., KILIÇ M. K., YÜKSEL D.
Acta Neurologica Belgica , cilt.122, sa.6, ss.1575-1581, 2022 (SCI-Expanded, Scopus)

13. Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study

Günay Ç., Aykol D., Özsoy Ö., Sönmezler E., BALIK Y. S., KARA B., et al.
Neuropediatrics , cilt.54, sa.4, ss.225-238, 2022 (SCI-Expanded, Scopus)

14. Pediatric dysphagia overview: best practice recommendation study by multidisciplinary experts

KARACA UMAY E., Eyigor S., GİRAY E., Karadag Saygi E., KARADAĞ B. T., Durmus Kocaaslan N., et al.
World Journal of Pediatrics , cilt.18, sa.11, ss.715-724, 2022 (SCI-Expanded, Scopus)

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

YILMAZ Ü., Gücüyener K., Yavuz M., Öncel İ., CANPOLAT M., ÜNVER O., et al.
European Journal of Paediatric Neurology , cilt.41, ss.8-18, 2022 (SCI-Expanded, Scopus)

16. Evaluation of Visual Evoked Potentials in Children with Neurofibromatosis Type 1 and Comparison With Radiological Findings Nörofibromatozis Tip 1 Tanılı Çocuklarda Desen Görsel Uyarılmış Potansiyellerin Değerlendirilmesi ve Radyolojik Bulgularla Karşılaştırılması

Öztoprak Ü., Aksoy E., CEYLAN N., Ekşioğlu A. S., YÜKSEL D.
Genel Tip Dergisi , cilt.32, sa.2, ss.144-149, 2022 (Scopus, TRDizin) Creative Commons License

17. Clinically mild encephalitis/encephalopathy with a reversible splenial lesion of the corpus callosum in childhood: a single-center experience

Çelik H., Derinkuyu B. E., Aksoy E., Öztoprak Ü., CEYLAN N., Azapağasi E., et al.
Turkish Journal of Medical Sciences , cilt.52, sa.2, ss.405-412, 2022 (SCI-Expanded, Scopus, TRDizin)

18. Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: A single center experience

Olgac A., Kasapkara Ç. S., Derinkuyu B., YÜKSEL D., ÇETİNKAYA S., Aksoy A., et al.
Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.9, ss.1169-1179, 2021 (SCI-Expanded, Scopus)

19. Expanding the genotype-phenotype spectrum of autosomal recessive charcot-marie-tooth disease: A novel plekhg5 gene mutation

YAYICI KÖKEN Ö., Öztoprak Ü., Topçu V., Çavdarli B., TEMUÇİN Ç. M., Aydingöz Ü., et al.
Neurology Asia , cilt.26, sa.3, ss.607-612, 2021 (SCI-Expanded, Scopus) Creative Commons License

20. Longitudinally extensive transverse myelitis in childhood: Clinical features, treatment approaches, and long-term neurological outcomes

Celik H., Aksoy E., Oztoprak U., CEYLAN N., Aksoy A., Yazici M. U., et al.
Clinical Neurology and Neurosurgery , cilt.207, 2021 (SCI-Expanded, Scopus)

21. Evaluation of the clinical characteristics of children with autism spectrum disorder and epilepsy and the perception of their parents on quality of life

Celik H., AÇIKEL S. B., ÖZDEMİR M., Aksoy E., Oztoprak U., CEYLAN N., et al.
Epilepsy Research , cilt.172, 2021 (SCI-Expanded, Scopus)

22. Evaluation of the Anxiety Level of Mothers of Children with Epilepsy during the COVID-19 Pandemic Period

Celik H., AÇIKEL S. B., Ozdemir F. M. A., Aksoy E., Oztoprak U., Cucu E., et al.
European Neurology , cilt.84, sa.3, ss.192-199, 2021 (SCI-Expanded, Scopus)

23. Spike-Wave Index Assessment and Electro-Clinical Correlation in Patients with Encephalopathy Associated with Epileptic State During Slow Sleep (ESES / CSWS); Single-Center Experience

Öztoprak Ü., YAYICI KÖKEN Ö., Aksoy E., YÜKSEL D.
Epilepsy Research , cilt.170, 2021 (SCI-Expanded, Scopus)

24. A rare case of intoxication related to concurrent exposure to butane gas and energy drink

CEYLAN N., Özdemir F. M. A., Çelik H., Azapagası E., Uysal Yazıcı M., YÜKSEL D.
Journal of Substance Use , cilt.26, sa.3, ss.225-227, 2021 (SSCI, Scopus)

25. Clinical characteristics and neurological findings of pediatric patients with acute carbon monoxide intoxication

Öztoprak Ü., Aksoy E., YAYICI KÖKEN Ö., Danış A., Ekşioğlu A. S., TUYGUN N., et al.
Journal of Pediatric Research , cilt.8, sa.1, ss.20-28, 2021 (ESCI, Scopus, TRDizin)

26. Acute necrotizing encephalopathy of childhood: A single-center experience

Aksoy E., Öztoprak Ü., Çelık H., Özdemır F. M. A., Özkan M., Kayalioğlu H., et al.
Turkish Journal of Medical Sciences , cilt.51, sa.2, ss.706-715, 2021 (SCI-Expanded, Scopus, TRDizin)

27. Hyperekplexia: A surprise diagnosis

YAYICI KÖKEN Ö., Dedeoglu Ö. T., Aksoy A., YÜKSEL D.
Neurologia i Neurochirurgia Polska , cilt.54, sa.5, ss.473-474, 2020 (SCI-Expanded, Scopus) Creative Commons License

28. A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation

Olgac A., Öztoprak Ü., Kasapkara Ç. S., KILIÇ M. K., YÜKSEL D., Derinkuyu E. B., et al.
Journal of Pediatric Endocrinology and Metabolism , cilt.33, sa.1, ss.165-170, 2020 (SCI-Expanded, Scopus)

29. Clinical and laboratory properties of pediatric acute infectious myositis: Evaluation of 26 patients Pedıatrık akut enfeksıyöz mıyozıtlerın klınık ve laboratuvar özellıklerı: 26 hastanin değerlendırılmesı

Danış A., YAYICI KÖKEN Ö., Kayılıoğlu H., Dedeoglu Ö., Aksoy A., YÜKSEL D.
Guncel Pediatri , cilt.18, sa.1, ss.95-103, 2020 (ESCI, Scopus)

30. Three pediatric cases of accidental levetiracetam overdose administration for long term

YAYICI KÖKEN Ö., Öztoprak Ü., Daniş A., Aksoy A., YÜKSEL D.
Turkiye Klinikleri Pediatri , cilt.28, sa.1, ss.51-54, 2019 (Scopus, TRDizin)

31. A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy

Aydin K., Aydin K., Akbas Y., ÜNAY B., ARSLAN M., CANSU A., et al.
Clinical Nutrition ESPEN , cilt.26, ss.27-34, 2018 (Scopus)

32. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

YILMAZ Ü., Anlar B., Gücüyener K., Yaramış A., CANSU A., ÜNALP A., et al.
European Journal of Paediatric Neurology , cilt.21, sa.6, ss.864-872, 2017 (SCI-Expanded, Scopus)

33. How does B12 deficiency of mothers affect their infants?

Tanyildiz H. G., Yesil S., Okur I., YÜKSEL D., ŞAHİN G.
Iranian Journal of Pediatrics , cilt.27, sa.5, 2017 (SCI-Expanded, Scopus)

34. Are the methylenetetrahydrofolate reductase 1298 and 677 gene polymorphisms related to optic glioma and hamartoma risk in neurofibromatosis type 1 patients?

Tanyıldız H. G., Yeşil Ş., Bozkurt C., Çandır M. O., Akpınar-Tekgündüz S., Toprak Ş., et al.
Turkish Journal of Pediatrics , cilt.58, sa.2, ss.152-158, 2016 (SCI-Expanded, Scopus, TRDizin)
Metrikler

Yayın

34

Yayın (WoS)

31

Yayın (Scopus)

34

H-İndeks (WoS)

8

Atıf (Scopus)

236

H-İndeks (Scopus)

8

Proje

1

Tez Danışmanlığı

13

Açık Erişim

13