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1دورية أكاديمية
المؤلفون: 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
المصدر: BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-8 (2024)
مصطلحات موضوعية: Contractures, DYSF, Dysferlinopathy, Limb-girdle muscle dystrophy R2, Spine rigidity, Diseases of the musculoskeletal system, RC925-935
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2474
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المؤلفون: Aleksandr A. Emelyantsev, Sergey N. Bardakov, Igor’ V. Boikov, Vladimir N. Malakhovskiy, Tamara E. Rameshvili, Vadim A. Tsargush, Gennadiy G. Romanov, Anna A. Bagrova
المصدر: Russian Military Medical Academy Reports. 41:23-30
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::51b0d34b342b42ef0e4e8d86cf2d7441
https://doi.org/10.17816/rmmar104383 -
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المؤلفون: 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
المساهمون: Centre de Recherche en Myologie, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Kazan Federal University (KFU), Centre de recherche en Myologie – U974 SU-INSERM
المصدر: Journal of Neuromuscular Diseases
Journal of Neuromuscular Diseases, IOS Press, 2020, pp.1-12. ⟨10.3233/JND-200476⟩مصطلحات موضوعية: 0301 basic medicine, Research Report, Male, medicine.medical_specialty, Contracture, Genotype, Ullrich congenital muscular dystrophy, [SDV]Life Sciences [q-bio], COL6A1, Mutation, Missense, Collagen Type VI, Biology, leaky splicing, Muscular Dystrophies, 03 medical and health sciences, Exon, 0302 clinical medicine, type VI collagen, Collagen VI, Internal medicine, fibroblasts, medicine, Missense mutation, Humans, Sibling, Myopathy, collagenopathy, Bethlem myopathy, Infant, Exons, Middle Aged, medicine.disease, contractures, Introns, 030104 developmental biology, Endocrinology, Phenotype, Neurology, Biological Variation, Population, myosclerotic phenotype of Bethlem myopathy, Mutation, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2f1397fdf700dced3ab8143a7c49f6
http://europepmc.org/articles/PMC8075389 -
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المؤلفون: 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
المصدر: Acta Myologica
مصطلحات موضوعية: Muscular Diseases, Muscular Dystrophies, Limb-Girdle, MRI pattern, Miyoshi myopathy, Humans, Original Article, T2-MSME, Muscle, Skeletal, Magnetic Resonance Imaging, dysferlinopathy, LGMDR2, LGMD2B
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cac65c3e0baec8f89ba370b49b293eef
https://pubmed.ncbi.nlm.nih.gov/35047756
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