S. S. Nikitin - Centre for Medical Genetics, Research

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论文共 66 篇作者统计合作学者相似作者

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Expanding the Spectrum of Clinical and Genetic Characteristics of Distal Arthrogryposis Type 5 Caused by Heterozygous Variants in the PIEZO2 Gene

E. L. Dadali,T. V. Markova,E. A. Melnik,S. S. Nikitin,I. V. Sharkova,O. V. Khalanskaya, L. A. Bessonov,E. A. Shestopalova,O. P. Ryzhkova,S. I. Trofimova,O. E. Agranovich,S. I. Kutsev

Нервно-мышечные болезниno. 2 (2024)

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Transcranial Magnetic Stimulation in Assessing the Functional Capacity of the Corticospinal Tract in Children

D. S. Kanshina,T. A. Akhadov,V. P. Zykov, S. A. Valliulina,V. N. Blokhina,S. S. Nikitin

Нервно-мышечные болезниno. 2 (2024)

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Phenotypic Variability in TRPV4-associated Neuropathies and Neuronopathies: a Case Series

A. F. Murtazina, P. N. Tsabay,G. E. Rudenskaya,L. A. Bessonova, F. M. Bostanova,D. M. Guseva,I. V. Sharkova,O. A. Shchagina,A. A. Orlova,O. P. Ryzhkova, T. V. Markova, A. S. Kuchina,S. S. Nikitin,E. L. Dadali

Нервно-мышечные болезниno. 2 (2023): 42-55

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Consensus Concept of Modern Effective Therapy for Duchenne Muscular Dystrophy

T. A. Gremyakova, S. B. Artemyeva,E. N. Baybarina,N. D. Vashakmadze,V. I. Guzeva,E. V. Gusakova,L. M. Kuzenkova, A. E. Lavrova, O. A. Lvova,S. V. Mikhaylova,L. P. Nazarenko,S. S. Nikitin,A. V. Polyakov,E. L. Dadali,A. G. Rumyantsev,G. E. Sakbaeva, V. M. Suslov, O. I. Gremyakova,A. A. Stepanov, N. I. Shakhovskaya

Neuromuscular Diseasesno. 2 (2023): 10-19

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Clinical and Genetic Characteristics of Type 7 Distal Arthrogryposis Caused by a Pathogenic Variant in the MYH8 Gene

I. V. Sharkova,S. S. Nikitin,T. V. Markova, A. E. Voskanyan,E. A. Melnik,O. A. Shchagina,E. L. Dadali

Neuromuscular Diseasesno. 3 (2023): 64-70

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Socioeconomic Efficiency of Neonatal Screening for Spinal Muscular Atrophy in the Russian Federation

I. A. Komarov,A. R. Malakhova, T. P. Vasilyeva, E. Yu. Shukan,O. Yu. Aleksandrova,R. A. Zinchenko, A. V. Polyakov,S. S. Nikitin,E. Yu. Sapego,S. I. Kutsev

Нервно-мышечные болезниno. 3 (2023): 25-32

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After-discharge Activity As a Basis to Change Intraoperative Mapping Protocol for Functionally Significant Brain Areas

M. G. Podgurskaya,D. S. Kanshina,A. V. Dimertsev,M. V. Alexandrov,S. S. Nikitin

Epilepsy and Paroxysmal Conditionsno. 1 (2023): 36-43

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Clinical and Genetic Characteristics of the First Russian Patient with a Syndrome of Craniofacial Dysmorphia-Deafness-anomalies of the Upper Limbs, Caused by a Mutation in the PAX3 Gene

T. V. Markova, V. V. Mavlyukeeva, B. G. Ginzburg,O. A. Shchagina,S. S. Nikitin,E. L. Dadali

Neuromuscular Diseasesno. 3 (2023): 48-53

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Clinical and Genetic Characteristics of Primary Hypertrophic Osteoarthropathy

E. L. Dadali, T. V. Markova,V. M. Kenis,T. S. Nagornova,S. S. Nikitin

Нервно-мышечные болезниno. 2 (2023): 56-63

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Stimulus-induced Periodic Discharges in Response to Low-Frequency Photostimulation in a Female Patient in Recovery Period after Middle Cerebral Artery Stroke

D. S. Kanshina, I. V. Okuneva,M. A. Surma,O. Yu. Bronov,S. S. Nikitin

Epilepsy and Paroxysmal Conditionsno. 3 (2023): 275-281

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