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Epilepsy and paroxysmal conditions

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Vol 14, No 1 (2022) Epilepsy in Norrie disease Abstract  similar documents
V. A. Aysina, О. V. Kozhevnikova, О. V. Osipova, A. V. Lashkova
 
Vol 4, No 4 (2012) BRAIN BLOOD FLOW EXAMINATION WITH HIGH-FLOOR MRI-PERFUSION DURING THE ATTACK OF MIGRAINE WITHOUT AURA Abstract  similar documents
M. I. Koreshkina, A. D. Khalikov, Yu. V. Nazinkina, V. V. Osipova, A. V. Amelin, E. A. Kosmacheva
 
Vol 13, No 3 (2021) Assessing efficacy and safety of rectally vs. intravenously administered Sibazon in treatment of generalized epileptic seizures in children Abstract  similar documents
A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanov, G. A. Osipova
 
Vol 13, No 2 (2021) Assessing efficacy and safety of buccally inoculated midazolam and intravenously administered diazepam for relieving pediatric primary generalized epileptic seizures Abstract  similar documents
A. G. Prityko, K. V. Osipova, P. L. Sokolov, E. A. Ezhova, I. G. Kotel’nikova, E. G. Lukyanova, G. A. Osipova
 
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
 
Vol 8, No 1 (2016) EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY Abstract  similar documents
E. G. Lukyanova, S. O. Ayvazyan, K. V. Osipova, T. N. Sorvacheva, E. A. Pyreva
 
Vol 10, No 4 (2018) Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases Abstract  similar documents
M. B. Mironov, N. V. Chebanenko, S. O. Ayvazyan, S. A. Vladimirova, K. V. Osipova, S. G. Burd, Yu. V. Rubleva, T. M. Krasilshchikova, V. G. Bychenko
 
Vol 14, No 3 (2022) Whole-exome sequencing of patients with juvenile myoclonic epilepsy Abstract  similar documents
E. E. Timechko, O. S. Shilkina, N. V. Oreshkova, V. O. Kobanenko, E. A. Osipova, N. A. Shnayder, D. V. Dmitrenko
 
Vol 11, No 1 (2019) Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko
 
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
 
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
 
Vol 15, No 4 (2023) DEPDC5-related familial focal epilepsy Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, L. M. Sushko, E. G. Lukyanova, K. V. Osipova, A. I. Krapivkin, N. N. Zavadenko
 
Vol 16, No 1 (2024) SEMA6B-related progressive myoclonus epilepsy in a patient with Klinefelter syndrome Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, L. M. Sushko, K. V. Osipova, A. M. Mazur, S. S. Fomenko, A. I. Krapivkin, N. N. Zavadenko
 
Vol 15, No 3 (2023) SPTAN1-associated developmental and epileptic encephalopathy Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Lukyanova, E. S. Bolshakova, S. O. Ayvazyan, K. V. Osipova, P. A. Vlasov, A. I. Krapivkin, N. N. Zavadenko
 
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