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Quoted phrase not found in phrase index: "Congenital myotonia, autosomal dominant form"
Page 1
Drug treatment for myotonia.
Cochrane Database Syst Rev. 2006 Jan 25;2006(1):CD004762. doi: 10.1002/14651858.CD004762.pub2.
Cochrane Database Syst Rev. 2006.
PMID: 16437496
Free PMC article.
Review.
The primary outcome measure was:reduced clinical myotonia using two categories: (1) no residual myotonia or improvement of myotonia or (2) No change or worsening of myotonia. ...MAIN RESULTS: Nine randomised controlled trials were found comparing activ …
The primary outcome measure was:reduced clinical myotonia using two categories: (1) no residual myotonia or improvement of …
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.
Marinella G, Orsini A, Scacciati M, Costa E, Santangelo A, Astrea G, Frosini S, Pasquariello R, Rubegni A, Sgherri G, Corsi M, Bonuccelli A, Battini R.
Marinella G, et al.
Genes (Basel). 2023 Jun 28;14(7):1363. doi: 10.3390/genes14071363.
Genes (Basel). 2023.
PMID: 37510268
Free PMC article.
Review.
BACKGROUND: Congenital myopathies are a group of clinically, genetically, and histologically heterogeneous diseases caused by mutations in a large group of genes. ...CONCLUSIONS: Our patient presented a phenotype compatible with the mild-moderate form, although she …
BACKGROUND: Congenital myopathies are a group of clinically, genetically, and histologically heterogeneous diseases caused by mutatio …
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