Доц. д-р Ülkühan Öztoprak — Pediatric Neurology

Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohortÜstün C., Polat İ., ÖZTÜRK G., ÜNVER O., TÜRKDOĞAN D., Kanmaz S., et al.Neuromuscular Disorders, cilt.67, 2026 (SCI-Expanded, Scopus)
Phenotypic continuum in IGHMBP2-related disorders: a portfolio of cases from typical to Guillain-Barré syndrome-like presentationBektaş H., Şener N., Bilgin N., ÜREL DEMİR G., Öncel İ., ÖZTOPRAK Ü., et al.Neuromuscular Disorders, cilt.59, 2026 (SCI-Expanded, Scopus)
Assessment of cardiac involvement in childhood neurofibromatosis type 1 diagnoses, identification of Rasopathic Casestekdemir i. e., Kayılıoğlu H., Doğan V., Aksoy A., Öztoprak Ü., aksoy e., et al.Health sciences quarterly (Online), cilt.6, sa.1, ss.139-146, 2026 (TRDizin)
Long-Term Clinical Characterization of ENTPD1-Related Spastic Paraplegia: A Novel Variant and Comprehensive Literature ReviewERKAN KOLAÇ D. D., Lafci O., ÖZTOPRAK Ü., Haliloglu G., GÜLERAY LAFCI N.INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, cilt.85, sa.5, 2025 (SCI-Expanded, Scopus)
Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotypeHaliloglu G., Donkervoort S., ÖZTOPRAK Ü., Osei-Owusu I. A., Pais L., Devrez F. D., et al.NEUROMUSCULAR DISORDERS, cilt.48, 2025 (SCI-Expanded, Scopus)
Frequency and Characteristics of Sleep Apnea Syndrome in Pediatric Patients with Duchenne Muscular DystrophyYavuz B. C., Yildiz S. O., Buyuksahin H. N., ÖZEL E., EMİRALİOĞLU ORDUKAYA N., AYKAN H. H., et al.EUROPEAN RESPIRATORY JOURNAL, 2024 (SCI-Expanded, Scopus)
Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromesYilmaz U., GÜCÜYENER K., Yavuz M., Oncel İ. H., CANPOLAT M., Saltik S., et al.EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, ss.8-18, 2022 (SCI-Expanded, Scopus)
Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutationYayici Koken O., Oztoprak Ü., Topcu V., Cavdarli B., Temuçin Ç. M., Aydıngöz Ü., et al.NEUROLOGY ASIA, cilt.26, sa.3, ss.607-612, 2021 (SCI-Expanded, Scopus)
Acute necrotizing encephalopathy of childhood: a single-center experienceAksoy E., Oztoprak Ü., Celik H., Ozdemir F. M. A., Ozkan M., Kayalioglu H., et al.TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.51, sa.2, ss.706-715, 2021 (SCI-Expanded, Scopus, TRDizin)
Clinical presentation of anti-N-methyl-D-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 casesKonuskan B., Yildirim M., Topaloglu H., Erol I., Oztoprak Ü., Tan H., et al.EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, cilt.22, sa.1, ss.135-142, 2018 (SCI-Expanded, Scopus)
The seizure semiology consistent with frontal lobe symptomatogenic zone in childrenOztoprak Ü., Yalnızoğlu D., Oguz K. K., Ergün E., Soylemezoglu F., Bilginer B., et al.TURKISH JOURNAL OF PEDIATRICS, cilt.58, sa.6, ss.583-591, 2016 (SCI-Expanded, Scopus, TRDizin)

Ülkühan Öztoprak

Publications

Articles 11

Conference papers 1

Контакты