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Epilepsy and paroxysmal conditions

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Vol 13, No 1 (2021) Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko
"... with epilepsy, hearing loss and mental retardation  syndrome (MIM 616577). Paired parents were carriers of one ..."
 
Vol 8, No 2 (2016) TREATMENT OF EPILEPSY IN TUBEROUS SCLEROSIS Abstract  similar documents
E. D. Belousova, M. Y. Dorofeeva, T. G. Ohapkina
"... with development of mental retardation in TSC. Early treatment of epilepsy is a key to prevention of mental ..."
 
Vol 10, No 2 (2018) Chromatography-tandem MASS spectrometry (HPLC-MS/MS) for the detection of valproic acid and its metabolites in blood plasma Abstract  similar documents
A. S. Malygin, N. S. Popov, M. A. Demidova, M. N. Kudrayshova
"... (10:90 v/v, 0.5 ml/min). The multiple ions monitoring (MIM) mode was used for mass- spectrometric ..."
 
Vol 5, No 2 (2013) FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY) Abstract  similar documents
M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin
"... healthy infant without focal signs or psychomotor retardation and not associated with epileptiform ..."
 
Vol 3, No 2 (2011) ISSUES OF RELAPSES IN ADULT PATIENTS WITH EPILEPSY Abstract  similar documents
V. A. Karlov, E. M. Rokotyanskaya, G. A. Kovalenko
"... surveyed and analysed 104 patients with an epilepsy, without expressed mental retardation, observed ..."
 
Vol 12, No 1 (2020) Childhood autism associated with neurological manifestations and corpus callosum hypoplasia: literature review and clinical cases Abstract  similar documents
O. A. Komissarova, O. A. Milovanova, G. G. Avakyan, S. V. Bugriy
"... associated with severe mental retardation, lack of verbal means of communication, motor stereotypes ..."
 
Vol 7, No 1 (2015) SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION Abstract  similar documents
I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan
"... encephalopaties leading to mental retardation, motor and speech disorders. ..."
 
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
"... / speech retardation were examined. We used the next generation sequencing (NGS) technique, which ..."
 
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
"... retardation. A video EEG monitoring test detected multiple EEG negative multifocal myoclonic episodes ..."
 
Vol 7, No 2 (2015) PERCEIVED WAYS OF DIAGNOSTIC HELP OPTIMISATION TO PATIENTS WITH SYMPTOMATIC EPILEPSY ON CHRONIC HERPESVIRUS ENCEPHALITIS Abstract  similar documents
N. A. Shnayder, N. I. Kamzalakova, S. V. Krijanovskaya, Yu. S. Panina
"... .4% encephalitis with epilepsy. Reduced hearing afferentation observed less frequently (24.1% vs. 26 ..."
 
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