Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vadim A. Tsargush"'
Autor:
Sergey N. Bardakov, Angelina A. Titova, Sergey S. Nikitin, Valentin Nikitins, Margarita O. Sokolova, Vadim A. Tsargush, Elena A. Yuhno, Oleg V. Vetrovoj, Pierre G. Carlier, Yana V. Sofronova, Аrtur А. Isaev, Roman V. Deev
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-8 (2024)
Abstract Background Dysferlinopathy is a phenotypically heterogeneous group of hereditary diseases caused by mutations in the DYSF gene. Early contractures are considered rare, and rigid spine syndrome in dysferlinopathy has been previously reported
Externí odkaz:
https://doaj.org/article/33b3ec8b75d34bd1862d731412b97b9a
Autor:
Aleksandr A. Emelyantsev, Sergey N. Bardakov, Igor’ V. Boikov, Vladimir N. Malakhovskiy, Tamara E. Rameshvili, Vadim A. Tsargush, Gennadiy G. Romanov, Anna A. Bagrova
Publikováno v:
Russian Military Medical Academy Reports. 41:23-30
Rhabdomyolysis is a life-threatening skeletal muscle disease, the time of diagnosis and initiation of treatment of which directly affects the likelihood of developing acute kidney injury and the quality of recovery of muscle function. The ultrasound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51b0d34b342b42ef0e4e8d86cf2d7441
https://doi.org/10.17816/rmmar104383
https://doi.org/10.17816/rmmar104383
Autor:
Vadim A. Tsargush, Roman V. Deev, Angelina Titova, V.L. Zorin, Patimat G. Akhmedova, Isaev Artur Aleksandrovich, M O Mavlikeev, C. Gartioux, Sergey N. Bardakov, Raisat M. Magomedova, Fedor A. Konovalov, Valérie Allamand, Zoya R. Umakhanova, Ekaterina N. Chernets, Gimat D. Dalgatov, Kamil Z. Zulfugarov
Publikováno v:
Journal of Neuromuscular Diseases
Journal of Neuromuscular Diseases, IOS Press, 2020, pp.1-12. ⟨10.3233/JND-200476⟩
Journal of Neuromuscular Diseases, IOS Press, 2020, pp.1-12. ⟨10.3233/JND-200476⟩
International audience; A family of five male siblings (three survivors at 48, 53 and 58 years old; two deceased at 8 months old and 2.5 years old) demonstrating significant phenotypic variability ranging from intermediate to the myosclerotic like Be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2f1397fdf700dced3ab8143a7c49f6
http://europepmc.org/articles/PMC8075389
http://europepmc.org/articles/PMC8075389
Autor:
Sergey N, Bardakov, Vadim A, Tsargush, Pierre G, Carlier, Sergey S, Nikitin, Sergey A, Kurbatov, Angelina A, Titova, Zoya R, Umakhanova, Patimat G, Akhmedova, Raisat M, Magomedova, Igor S, Zheleznyak, Alexander A, Emelyantsev, Ekaterina N, Berezhnaya, Ivan, A Yakovlev, Artur A, Isaev, Roman V, Deev
Publikováno v:
Acta Myologica
The widespread use of magnetic resonance imaging (MRI) in the diagnosis of myopathies has made it possible to clarify the typical MRI pattern of dysferlinopathy. However, sufficient attention has not been given to the variability of MRI patterns in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cac65c3e0baec8f89ba370b49b293eef
https://pubmed.ncbi.nlm.nih.gov/35047756
https://pubmed.ncbi.nlm.nih.gov/35047756