Results 91 to 100 of about 39,732 (154)

A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A. [PDF]

open access: yesNeurology, 2009
Rajakulendran S   +8 more
europepmc   +1 more source

Treatment updates in myotonic disorders. [PDF]

open access: yesJ Neurol
Matthews E, Specterman MJ, Mul K.
europepmc   +1 more source

Paramyotonia Congenita

open access: yes, 1966
Arthur J. Hudson
core   +2 more sources

Recurrent Severe Viral-Induced Rhabdomyolysis Associated With Underlying Genetic Variants in a Young Adult: A Case Report. [PDF]

open access: yesCureus
Stone AM   +13 more
europepmc   +1 more source

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