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Neuropediatrics|May 22, 2012
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, et al.Journal of Child Neurology|January 30, 2010
Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI)Zulfikar Arlier, Yasar Bayri, Luis E Kolb, et al.Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegenerationKaya Bilguvar, Navneet K Tyagi, Cigdem Ozkara, et al.Neurological Research|May 2, 2025
Clinical characteristics and prognostic clinical factors of anti-gamma-aminobutyric acid-B receptor (GABAB-R) encephalitis in Türkiye: a multicenter studyRabia Gokcen Gozubatik-Celik, Betul Baykan, Ahmed Serkan Emekli, et al.Pageof 2