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]
Rajakulendran S +8 more
europepmc +1 more source
Mitochondrial dysfunction in hyperkalemic periodic paralysis: A case report and literature review. [PDF]
Mikhael FG +3 more
europepmc +1 more source
Treatment updates in myotonic disorders. [PDF]
Matthews E, Specterman MJ, Mul K.
europepmc +1 more source
Myotonia: Recognition, Evaluation, and Differential Diagnosis. [PDF]
Crayle JI, Al-Lozi M, Miller TM.
europepmc +1 more source
Lifestyle and dietary measures in Periodic Paralyses. [PDF]
Politano L.
europepmc +1 more source
Recurrent Severe Viral-Induced Rhabdomyolysis Associated With Underlying Genetic Variants in a Young Adult: A Case Report. [PDF]
Stone AM +13 more
europepmc +1 more source
Neurogenic Paradoxical Vocal Fold Motion: A Systematic Review of Central and Pheripheral Nervous System Disorders. [PDF]
Gyawali BR +3 more
europepmc +1 more source

