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Journal of Child Neurology|August 11, 2007
Impact of recent seizures on cerebral blood flow in patients with sturge-weber syndrome: study of 2 casesKader K Oguz, Senem Senturk, Arzu Ozturk, et al.Journal of Child Neurology|August 2, 2002
Gender prevalence in childhood multiple sclerosis and myasthenia gravisGoknur Haliloglu, Banu Anlar, Sabiha Aysun, et al.European Journal of Pediatrics|September 28, 2017
Niemann-Pick disease type C in the newborn period: a single-center experienceErsin Gumus, Goknur Haliloglu, Asuman Nur Karhan, et al.Journal of Child Neurology|February 10, 2018
Neurologic Involvement in Primary Immunodeficiency DisordersMirac Yildirim, Deniz Cagdas Ayvaz, Bahadir Konuskan, et al.Epilepsy & Behavior : E&B|July 1, 2020
Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experienceDilek Yalnizoglu, Didem Ardicli, Burcak Bilginer, et al.Human Genome Variation|May 25, 2019
Clinical outcomes of two patients with a novel pathogenic variant in ASNS: response to asparagine supplementation and review of the literatureRosanne Sprute, Didem Ardicli, Kader Karli Oguz, et al.Journal of Neuroimmunology|June 25, 2022
Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophiesNesibe Gevher Eroglu-Ertugrul, Mohammadreza Yousefi, Faruk Pekgül, et al.Brain : a Journal of Neurology|February 10, 2009
Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosisMaria Kousi, Eija Siintola, Lenka Dvorakova, et al.American Journal of Human Genetics|June 15, 2007
The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporterEija Siintola, Meral Topcu, Nina Aula, et al.Human Mutation|March 17, 2004
Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsySusanna Ranta, Meral Topcu, Saara Tegelberg, et al.Pageof 4