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Epilepsy and paroxysmal conditions

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Vol 16, No 2 (2024) A rare genetic Schuurs-Hoeijmakers syndrome (PACS1 syndrome) Abstract  similar documents
T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, A. D. Mikhailova, A. I. Krapivkin, N. N. Zavadenko
"... , эпилепсией и описанными вариантами в гене PACS1 (rs398123009, chr11:6621120, c.607C>T, p.Arg203Trp). Знание ..."
 
Vol 17, No 2 (2025) A novel X-linked immune-mediated actinopathy in a boy with anti-NMDA receptor encephalitis and variant in DOCK11 gene Abstract  similar documents
T. V. Kozhanova, S. S. Zhylina, T. I. Meshcheryakova, A. A. Abramov, M. M. Abidova, T. S. Kaminskaya, A. I. Krapivkin, N. N. Zavadenko
"... мальчика с выявленным гемизиготным вариантом в гене DOCK11. Дефицит DOCK11 – это новая иммуноопосредованная ..."
 
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
"... , ассоциированной с вариантами нуклеотидной последовательности в гене DEPDC5. Проведено клинико-генеалогическое ..."
 
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
"... Варианты нуклеотидной последовательности в гене SEMA6B в большинстве случаев обусловливают ..."
 
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
"... нуклеотидной последовательности в гене SPTAN1. Мутации в гене SPTAN1 описаны у пациентов с энцефалопатией ..."
 
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
"...  генов, ассоциированных с эпилептической энцефалопатией, выявлены ранее не описанные у больных варианты ..."
 
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