Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marie-Louise Stridh"'
Publikováno v:
European Journal of Physiotherapy. 19:24-31
Aims: To increase knowledge regarding postural control in congenital (CDM1) and childhood (ChDM1) forms of myotonic dystrophy type 1 and to analyze whether variations can be explained by age, joint motion, muscle strength and molecular findings.Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::086292500105b1c8dae5abf3ee353eff
https://doi.org/10.1080/21679169.2016.1229028
https://doi.org/10.1080/21679169.2016.1229028
Publikováno v:
Neuromuscular disorders : NMD. 27(9)
The aims of this study were to explore how motor function and muscle strength change over time in the congenital and childhood forms of myotonic dystrophy type 1, further to investigate whether sex, age, disease severity or size of the mutation could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b814b75755b27e8fd3bf1e2319df7d2b
https://pubmed.ncbi.nlm.nih.gov/28673557
https://pubmed.ncbi.nlm.nih.gov/28673557
Publikováno v:
Neuromuscular Disorders. 23:832-833
Myotonic dystrophy type 1 (DM1) is one of the more common neuromuscular disorders in childhood with strongly varying prevalence in different regions. The disorder is autosomal dominantly inherited and the genetic defect is due to a CTG trinucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26525fd380066ea02f20ef231c831a5d
https://doi.org/10.1016/j.nmd.2013.06.671
https://doi.org/10.1016/j.nmd.2013.06.671