Proximal spinal muscular atrophy types I-IV: Specific features of molecular genetic diagnosis by V. V. Zabnenkova, E. L. Dadali, A. V. Polyakov

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Clinical and genetic characteristics and diagnosis of hereditary variants of neonatal epilepsy by N. A. Semenova, E. L. Dadali, A. A. Sharkov, I. A. Akimova

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Comparative analysis of phenotypes features in two common genetic variants of limb-girdle muscular dystrophy by I. V. Sharkova, E. L. Dadali, I. V. Ugarov, O. P. Ryzhkova, A. V. Polyakov

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Cardiomyopathy of Friedreich's Disease. Modern Methods of Diagnostic by E. I. Fomicheva, R. P. Myasnikov, Y. A. Selivyorstov, S. N. Illarioshkin, E. L. Dadali, O. M. Drapkina

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Clinical and genetic characteristics of the early 66th type epileptic encephalopathy (literature review and own observation) by T. V. Markova, A. O. Borovikov, E. R. Lozier, A. A. Isaev, V. S. Kaimonov, E. A. Pomerantseva, F. A. Konovalov, O. A. Schagina, E. L. Dadali

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Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia by A. F. Murtazina, O. A. Shchagina, T. B. Milovidova, E. L. Dadali, G. E. Rudenskaya, S. A. Kurbatov, T. V. Fedotova, S. S. Nikitin, P. A. Sparber, M. D. Orlova, A. V. Polyakov

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