ALLMedicine™ Facioscapulohumeral Dystrophy Center
Research & Reviews 215 results
https://doi.org/10.1212/WNL.0000000000011412
Neurology Rieken A, Bossler AD et. al.
Jan 14th, 2021 - To summarize facioscapulohumeral muscular dystrophy (FSHD) diagnostic testing results from the University of Iowa Molecular Pathology Laboratory. All FSHD tests performed in the diagnostic laboratory from January 2015 to July 2019 were retrospecti...
https://doi.org/10.1136/jmedgenet-2020-107041
Journal of Medical Genetics; Lemmers RJLF, van der Vliet PJ et. al.
Jan 13th, 2021 - Facioscapulohumeral dystrophy (FSHD) is an inherited muscular dystrophy clinically characterised by muscle weakness starting with the facial and upper extremity muscles. A disease model has been developed that postulates that failure in somatic re...
https://doi.org/10.1002/mus.27123
Muscle & Nerve; Hatch MN, Kurillo G et. al.
Nov 20th, 2020 - This study examines the correlation, and clinical meaningfulness, between reachable workspace outcome and reported activities of daily living (ADL) function of individuals with facioscapulohumeral dystrophy (FSHD). Twenty-one FSHD subjects with va...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571703
PloS One; Zhao ZF, Du L et. al.
Oct 19th, 2020 - Facioscapulohumeral dystrophy (FSHD) is characterized by a loss of repressive epigenetic marks leading to the aberrant expression of the DUX4 transcription factor. In muscle, DUX4 acts as a poison protein though the induction of multiple downstrea...
https://doi.org/10.1016/j.otsr.2020.03.002
Orthopaedics & Traumatology, Surgery & Research : OTSR; Eren İ, Birsel O et. al.
May 20th, 2020 - Scapulothoracic arthrodesis (STA) is a well-established surgical technique to provide scapular stabilisation in patients with facioscapulohumeral dystrophy (FSHD). There is no staging or scoring systems available to guide surgical decision. The ai...
Clinicaltrials.gov 215 results
https://doi.org/10.1212/WNL.0000000000011412
Neurology Rieken A, Bossler AD et. al.
Jan 14th, 2021 - To summarize facioscapulohumeral muscular dystrophy (FSHD) diagnostic testing results from the University of Iowa Molecular Pathology Laboratory. All FSHD tests performed in the diagnostic laboratory from January 2015 to July 2019 were retrospecti...
https://doi.org/10.1136/jmedgenet-2020-107041
Journal of Medical Genetics; Lemmers RJLF, van der Vliet PJ et. al.
Jan 13th, 2021 - Facioscapulohumeral dystrophy (FSHD) is an inherited muscular dystrophy clinically characterised by muscle weakness starting with the facial and upper extremity muscles. A disease model has been developed that postulates that failure in somatic re...
https://doi.org/10.1002/mus.27123
Muscle & Nerve; Hatch MN, Kurillo G et. al.
Nov 20th, 2020 - This study examines the correlation, and clinical meaningfulness, between reachable workspace outcome and reported activities of daily living (ADL) function of individuals with facioscapulohumeral dystrophy (FSHD). Twenty-one FSHD subjects with va...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571703
PloS One; Zhao ZF, Du L et. al.
Oct 19th, 2020 - Facioscapulohumeral dystrophy (FSHD) is characterized by a loss of repressive epigenetic marks leading to the aberrant expression of the DUX4 transcription factor. In muscle, DUX4 acts as a poison protein though the induction of multiple downstrea...
https://doi.org/10.1016/j.otsr.2020.03.002
Orthopaedics & Traumatology, Surgery & Research : OTSR; Eren İ, Birsel O et. al.
May 20th, 2020 - Scapulothoracic arthrodesis (STA) is a well-established surgical technique to provide scapular stabilisation in patients with facioscapulohumeral dystrophy (FSHD). There is no staging or scoring systems available to guide surgical decision. The ai...
