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A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation.

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Defective slow inactivation of sodium channels contributes to familial periodic paralysis

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The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channel.

Performance of an intramuscular electrode during functional neuromuscular stimulation for gait training post stroke.

A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation.

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Defective slow inactivation of sodium channels contributes to familial periodic paralysis

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