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Epilepsy and paroxysmal conditions

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Vol 11, No 4 (2019) Significance of exome sequencing for diagnosis of epilepsy in children Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
"... Introduction. Epilepsy is a neurological disorder characterized by periodic seizure attacks ..."
 
Vol 11, No 4 (2019) Early infantile epileptic encephalopathy type 16: the new clinical and genetic variant of TBC1D24 gene mutation Abstract  similar documents
A. A. Kholin, I. D. Fedonyuk, O. P. Dovelman, N. N. Zavadenko, T. V. Kozhanova, E. A. Kholina, G. Sh. Khondkarian, E. S. Il`ina
"... epileptic encephalopathy type 16 in a child with homozygous mutation in TBC1D24 gene. Material and methods ..."
 
Vol 12, No 1 (2020) Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
"... ) in patients with epileptic encephalopathy, ASD, and characteristic phenotype, it is advisable to take ..."
 
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