Search Results - A. G. Prityko

Congenital cerebral palsy with epilepsy: clinical and genetic comparisons by N. V. Chebanenko, P. L. Sokol, A. G. Prityko

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Genetic heterogeneity of congenital cerebral palsy and the concept of the neurotropic genome by P. L. Sokolov, N. V. Chebanenko, A. G. Prityko, P. A. Romanov

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Clinical and genetic parallels in congenital brain lesions without epilepsy by P. L. Sokolov, A. G. Prityko, N. V. Chebanenko, P. A. Romanov

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Significance of exome sequencing for diagnosis of epilepsy in children by T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

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Clinical case: experience in the treatment of hyperplastic gingivitis in a patient with poor oral hygiene by P. A. Voronin, A. G. Prityko, A. E. Kazakova, V. A. Voronin, I. A. Nikolskaya

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Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case by T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

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Clinical case of distal arthrogryposis in combination with epilepsy due to an unbalanced translocation by T. V. Kozhanova, S. S. Zhilina, T. I. Meshсheryakova, N. P. Prokopyeva, A. G. Prityko, N. N. Zavadenko

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Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder by T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

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THE GENETIC SUSCEPTIBILITY TO ATHEROSCLEROSIS by T. V. Kozhanova, E. V. Neudakhin, S. S. Zhilina, T. I. Mescheryakova, A. A. Abramov, E. N. Lukash, A. G. Prityko

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Genetic Aspects of Pathogenesis of Congenital Spastic Cerebral Paralysis by A. G. Prityko, N. V. Chebanenko, P. L. Sokolov, V. P. Zykov, O. V. Klimchuk, I. V. Kanivets

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Congenital cerebral palsy: genetic cause and nosological integrity by P. I. Sokolov, N. V. Chebanenko, V. P. Zykov, I. V. Kanivets, A. G. Prityko, P. A. Romanov

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Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene by 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

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Experience of application of proproceptive modeling of walking in children of early age with motor disorders by A. G. Prityko, N. V. Chebanenko, V. P. Zykov, P. L. Sokolov, E. A. Bukreeva, T. A. Sednenkova, E. Yu. Sergeenko

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Assessing efficacy and safety of buccally inoculated midazolam and intravenously administered diazepam for relieving pediatric primary generalized epileptic seizures by A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanova, G. A. Osipova

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Assessing efficacy and safety of rectally vs. intravenously administered Sibazon in treatment of generalized epileptic seizures in children by A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanov, G. A. Osipova

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New mutation in the TRIP4 gene associated with congenital muscular dystrophy Davignon–Chauveau type (clinical case) by T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, M. Yu. Shorina, I. F. Demenshin, G. G. Prokopiev, I. V. Kanivets, V. S. Suchorukov, P. L. Anufriev, T. I. Baranich, A. A. Kozina, A. G. Prityko

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Rehabilitation of children with cerebral palsy and epilepsy: an assessment of the effectiveness and safety by E. A. Bukreeva, T. A. Sednenkova, E. Yu. Sergeenko, N. V. Chebanenko, K. V. Osipova, O. A. Laisheva, I. A. Shavyrin, A. G. Prityko, D. V. Kovalev, V. P. Zykov, P. L. Sokolov, P. A. Romanov

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