Ülkühan Öztoprak

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures

Shenzhao Lu, Rebecca Hernan, Paul C. Marcogliese et al. · The American Journal of Human Genetics · 2022 · 39 citations · Full text

Neurodevelopmental Disorders, Genetic Disorder, Genetics +11

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

Ünsal Yılmaz, Banu Anlar, Kıvılcım Gücüyener et al. · European Journal of Paediatric Neurology · 2017 · 28 citations

Pediatric Multiple Sclerosis, Pediatric Epidemiology, Medicine +9

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

Ülkühan Öztoprak, Özlem Yayıcı Köken, Erhan Aksoy et al. · Epilepsy Research · 2021 · 27 citations

Neuropsychology, Neurological Disorder, Neurophysiological Biomarkers +17

A rare case of primary coenzyme Q10 deficiency due to <i>COQ9</i> mutation

Asburçe Olgaç, Ülkühan Öztoprak, Çiğdem Seher Kasapkara et al. · Journal of Pediatric Endocrinology and Metabolism · 2019 · 23 citations

Clinical presentation of anti-N-methyl- d -aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 cases

Bahadır Konuşkan, Haluk Topaloğlu, İlknur Erol et al. · European Journal of Paediatric Neurology · 2017 · 18 citations

Immunology, Pediatrics, Clinical Presentation +2