ALLMedicine™ Facioscapulohumeral Dystrophy Center
Research & Reviews 99 results
https://clinicaltrials.gov/ct2/show/NCT05239520
May 5th, 2022 - Shoulder instability in Facioscapulohumeral dystrophy (FSHD) is a significant problem, with over 80% of patients reporting that it affects their ability to perform activities of daily living (Faux-Nightingale , 2021). The underlying mechanisms of ...
https://doi.org/10.1080/01942638.2022.2068991
Physical & Occupational Therapy in Pediatrics; Fanuscu A, Bulut N et. al.
Apr 28th, 2022 - This study aims to investigate the feasibility and safety of short-term functional electrical stimulation (FES) training of the quadriceps femoris muscles in a child with facioscapulohumeral muscular dystrophy (FSHD). A 7-year-old child with FSHD ...
https://clinicaltrials.gov/ct2/show/NCT05199246
Mar 29th, 2022 - Patients with neuromuscular disorders display different type of symptoms depending on the type of pathology. Diseases like facioscapulohumeral dystrophy (FSHD), limb-girdle muscular dystrophy (LGMD2b), sporadic inclusion body myositis (SIBM) or Po...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890461
Orphanet Journal of Rare Diseases; Sanson B, Stalens C et. al.
Mar 4th, 2022 - Facioscapulohumeral muscular dystrophy (FSHD) is among the most prevalent muscular dystrophies and currently has no treatment. Clinical and genetic heterogeneity are the main challenges to a full comprehension of the physiopathological mechanism. ...
https://doi.org/10.1093/hmg/ddab364
Human Molecular Genetics; Wong CJ, Wang L et. al.
Dec 18th, 2021 - Advances in understanding the pathophysiology of facioscapulohumeral dystrophy (FSHD) have led to several therapeutic approaches entering clinical trials and an increased need to develop biomarkers of disease activity and progression. Multiple pri...
Clinicaltrials.gov 5 results
https://clinicaltrials.gov/ct2/show/NCT05239520
May 5th, 2022 - Shoulder instability in Facioscapulohumeral dystrophy (FSHD) is a significant problem, with over 80% of patients reporting that it affects their ability to perform activities of daily living (Faux-Nightingale , 2021). The underlying mechanisms of ...
https://clinicaltrials.gov/ct2/show/NCT05199246
Mar 29th, 2022 - Patients with neuromuscular disorders display different type of symptoms depending on the type of pathology. Diseases like facioscapulohumeral dystrophy (FSHD), limb-girdle muscular dystrophy (LGMD2b), sporadic inclusion body myositis (SIBM) or Po...
https://clinicaltrials.gov/ct2/show/NCT04267354
Feb 12th, 2020 - The investigators believe that arm cycling has the potential to be effective in maintaining or improving shoulder muscle functioning. However, there is no evidence for its safety or effectiveness in the upper extremity. The aim of the study is to ...
https://clinicaltrials.gov/ct2/show/NCT02625662
Sep 26th, 2019 - FSHD is a hereditary muscle disease with slowly progressive muscle weakness. In children it is a very heterogenic disease ranging from severely affected infants to mildly affected adolescents. Symptoms can include muscle weakness, pain, fatigue, e...
https://clinicaltrials.gov/ct2/show/NCT01116570
Apr 1st, 2015 - Our research project aims at establishing a program of physical training that will fulfill the two following conditions: (i) being compatible with the daily professional, social and family activity of the patients so it can be integrated in their ...
