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Просмотр по теме "Miyoshi myopathy"

Просмотр по теме "Miyoshi myopathy"

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  • Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front Neurol, 8, (2017) (77)] doi: 10.3389/fneur.2017.00077 
    Umakhanova Z.; Bardakov S.; Mavlikeev M.; Chernova O.; Magomedova R.; Akhmedova P.; Yakovlev I.; Dalgatov G.; Fedotov V.; Isaev A.; Deev R. (2017)
    The "Funding" section should be: This work was funded by Human Stem Cells Institute PJSC and Roman V. Deev. Theoretical part of this work was supported by Russian Scientific Foundation grant (14-15-00916). Ivan A. Yakovlev ...
  • Magnetic resonance imaging pattern variability in dysferlinopathy 
    Bardakov S.N.; Tsargush V.A.; Carlier P.G.; Nikitin S.S.; Kurbatov S.A.; Titova A.A.; Umakhanova Z.R.; Akhmedova P.G.; Magomedova R.M.; Zheleznyak I.S.; Emelyantsev A.A.; Berezhnaya E.N.; A Yakovlev I.; Isaev A.A.; Deev R.V. (2021)
    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 ...
  • Modeling and gene therapy of dysferlinopathy 
    Starostina I.; Solovyeva V.; Yuryeva K.; Shevchenko K.; Fedotov V.; Rizvanov A.; Deev R.; Isaev A. (2013)
    Dysferlinopathies is a group of autosomal-recessive inherited neuromuscular diseases, which are characterized by defect in mRNA expression or in functionioning of dysferlin protein, appearing in about 1/200 000 births. ...
  • Twenty-year clinical progression of dysferlinopathy in patients from Dagestan 
    Umakhanova Z.; Bardakov S.; Mavlikeev M.; Chernova O.; Magomedova R.; Akhmedova P.; Yakovlev I.; Dalgatov G.; Fedotov V.; Isaev A.; Deev R. (2017)
    © 2017 Umakhanova, Bardakov, Mavlikeev, Chernova, Magomedova, Akhmedova, Yakovlev, Dalgatov, Fedotov, Isaev and Deev.To date, over 30 genes with mutations causing limb-girdle muscle dystrophy have been described. ...

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