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Journal of Child Neurology|May 8, 2010
Multidrug resistance 1 (MDR1) gene polymorphisms in childhood drug-resistant epilepsyAsude Alpman, Ferda Ozkinay, Hasan Tekgul, et al.
Neuropediatrics|January 24, 2013
Diagnostic tools of early brain disturbances in an asymptomatic neonate with maple syrup urine diseaseDemet Terek, Ozge Koroglu, Mehmet Yalaz, et al.
Pediatric Neurology|August 10, 2010
Ratios of nine risk factors in children with recurrent febrile seizuresAyse Tosun, Guldane Koturoglu, Gul Serdaroglu, et al.
Epilepsy & Behavior : E&B|July 5, 2008
The effect of depression on academic achievement in children with epilepsyAyşe Tosun, Sezen Gokcen, Burcu Ozbaran, et al.
Acta Neurologica Belgica|October 14, 2016
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathySarenur Gokben, Huseyin Onay, Sanem Yilmaz, et al.
Epilepsy & Behavior : E&B|June 6, 2008
Semiologic seizure classification: the effectiveness of a modular education program for health professionals in pediatricsAysegul Isler, Zumrut Basbakkal, Gul Serdaroglu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 25, 2020
The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathiesEsra Isik, Sanem Yilmaz, Tahir Atik, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 28, 2020
Sulthiame add-on treatment in children with epileptic encephalopathy with status epilepticus: an efficacy analysis in etiologic subgroupsSeda Kanmaz, Erdem Simsek, Hepsen Mine Serin, et al.
Iranian Journal of Child Neurology|November 16, 2016
Molecular Genetic Analysis of Survival Motor Neuron Gene in 460 Turkish Cases with Suspicious Spinal Muscular Atrophy DiseaseAfrooz Rashnonejad, Huseyin Onay, Tahir Atik, et al.
Case Reports in Genetics|July 23, 2014
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan geneGulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, et al.
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