Differential approach to treating life-threatening arrhythmogenic conditions in patients with X-linked Emery—Dreifuss myopathy

by O. S. Groznova, G. E. Rudenskaya, T. A. Adyan, D. A. Kharlamov
Published 2016-03-01

Cardiac lesion in children with inherited neuromuscular diseases

by O. S. Groznova, G. E. Rudenskaya, T. A. Adyan, D. A. Kharlamov
Published 2016-03-01

Sakharnyy diabet pri ataksii Fridreykha

by O S Shcheglova, G E Rudenskaya, Tamara Leonidovna Kuraeva, S A Klyushnikov
Published 2000-12-01

Diversity of <i>VCP</i>-related phenotypes: case report and literature review

by G. E. Rudenskaya, O. L. Mironovich, A. F. Murtazina, O. A. Shchagina
Published 2021-04-01

Cardiovascular disorders in patients with X-linked Emery—Dreifuss progressive muscular dystrophy

by O. S. Groznova, D. A. Kharlamov, S. B. Artemyeva, G. E. Rudenskaya, T. A. Adyan, O. P. Ryzhkova
Published 2016-03-01

A case of hereditary motor and sensory neuropathy type IVA with unusual genealogy

by S. A. Kurbatov, T. B. Milovidova, V. P. Fedotov, A. F. Murtazina, G. E. Rudenskaya, O. A. Shchagina, A. V. Polyakov
Published 2018-07-01

Clinical and genetic characteristics of Nonaka myopathy (GNE-myopathy) in russian patients

by E. L. Dadali, I. V. Sharkova, G. E. Rudenskaya, S. S. Nikitin, A. F. Murtazina, O. P. Ryzhkova, A. L. Chukhrova
Published 2019-11-01

Early epileptic encephalopathy associated with SCN2A mutations: clinical and genetic description of eight novel patients

by E. L. Dadali, F. A. Konovalov, I. A. Akimova, A. A. Sharkov, G. E. Rudenskaya, S. V. Mikhaylova, S. A. Korostelev
Published 2018-07-01

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families

by G. E. Rudenskaya, V. A. Kadnikova, O. P. Ryzhkova, L. A. Bessonova, E. L. Dadali, D. S. Guseva, T. V. Markova, D. N. Khmelkova, A. V. Polyakov
Published 2020-08-01

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
Published 2020-08-01

A clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental retardation, autism, and movement disorders

by M.Yu Bobylova, M.B. Mironov, A.V. Kulikov, M.V Kazakova, M.A. Bogacheva, Yu.A. Tankevich, L.Yu. Glukhova, E.I Barletova, M.O. Abramov, K.Yu. Mukhin, G.E. Rudenskaya
Published 2014-06-01