Results 91 to 100 of about 365 (121)

Meeting report: the 2020 FSHD International Research Congress

Skeletal Muscle, 2020
Michael Kyba, Robert J. Bloch, Julie Dumonceaux, Scott Q. Harper, Silvère M. van der Maarel, Francis M. Sverdrup, Kathryn R. Wagner, Baziel van Engelen, Yi-Wen Chen   +8 more
doaj   +1 more source

Corrigendum: Sarcopenic Obesity in Facioscapulohumeral Muscular Dystrophy

Frontiers in Physiology, 2022
Kathryn Vera, Kathryn Vera, Mary McConville, Michael Kyba, Manda Keller-Ross, Manda Keller-Ross   +5 more
doaj   +1 more source

The history of research on facioscapulohumeral muscular dystrophy

Chinese Journal of Contemporary Neurology and Neurosurgery, 2019
Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary neuromuscular disease which is divided into FSHD1 and FSHD2. After years of research, FSHD has established complete molecular diagnostic methods, in which Southern blotting is commonly ...
Cheng ZHANG, Huan LI
doaj  

P557: Preimplantation genetic diagnosis for facioscapulohumeral muscular dystrophy

Genetics in Medicine Open, 2023
Hagit Shani, Baruch Feldman, Noa Harel Inbar, Haike Reznik-Wolf, Elon Pras   +4 more
doaj   +1 more source

Facioscapulohumeral muscular dystrophy.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2021
Jana, Pospisilova, Bård, Bjørnarå, Kari Anne, Bjørnarå   +2 more
openaire   +1 more source

Facioscapulohumeral muscular dystrophy [PDF]

, 2020
openaire   +2 more sources

Facioscapulohumeral muscular dystrophy

, 2018
Yuranga Weerakkody, Mohamed Saber, Craig Hacking   +2 more
openaire   +1 more source

Some of the next articles are maybe not open access.

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Facioscapulohumeral muscular dystrophy

Muscle and Nerve, 2006
AbstractFacioscapulohumeral muscular dystrophy (FSHD) is a dominantly inherited disorder with an initially restricted pattern of weakness. Early involvement of the facial and scapular stabilizer muscles results in a distinctive clinical presentation. Progression is descending, with subsequent involvement of either the distal anterior leg or hip‐girdle ...
Rabi Tawil, Silvere M Van Der Maarel
exaly   +5 more sources

Facioscapulohumeral muscular dystrophy

Current Opinion in Neurology, 2009
Knowledge of the pathogenetic mechanisms in facioscapulohumeral muscular dystrophy is still scattered, but has recently been advanced through novel developments on the genetic scientific front.The present brief review highlights some recent studies on the pathogenesis of facioscapulohumeral muscular dystrophy pointing to major involvement of muscle ...
Padberg, G.W.A.M., Engelen, B.G.M. van
openaire   +4 more sources

Facioscapulohumeral Muscular Dystrophy

Continuum
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy, affecting individuals across the lifespan with variable severity. This article provides an overview of the distinctive genetic mechanisms underlying FSHD, its clinical manifestations, including pediatric-specific features, treatment, and the evolving ...
Natalie K. Katz, Jeffrey M. Statland
  +5 more sources