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Paramyotonia congenita

Paramyotonia congenita of von eulenburg
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Paramyotonia congenita" returned 2 free, full-text review articles. First 2 results:
Overlap of periodic paralysis and paramyotonia congenita caused by SCN4A gene mutations two family reports and literature review.
Last Updated: Oct 01, 2019

To verify the diagnosis of channelopathies in two families and explore the mechanism of the overlap between periodic paralysis (PP) and paramyotonia congenita (PMC).

Paramyotonia congenita without cold paralysis: a case report.
Last Updated: Nov 21, 2008

A 27-year-old-woman with paramyotonia congenita was reported. She began to suffer from myotonia since infancy. Myotonia was aggravated by cold, but with intense cooling myotonia did not change to flaccid paralysis. Four generations of her family showed the same symptoms that suggested ...

Paramyotonia congenita.
Last Updated: Nov 16, 2005

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Paramyotonia congenita" returned 1 free, full-text editorial articles. First 1 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Paramyotonia congenita" returned 28 free, full-text research articles. First few results:
Open-label trial of ranolazine for the treatment of paramyotonia congenita.
Last Updated: Oct 08, 2019

Paramyotonia congenita (PMC) is a nondystrophic myotonic disorder that is believed to be caused by a defect in Na 1.4 sodium channel inactivation. Ranolazine, which acts by enhancing slow inactivation of sodium channels, has been proposed as a therapeutic option, but in vivo studies are lacking.

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28 Free Research Articles 101 Research Articles