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Publications by F van Landeghem
Progressive Muscle Atrophy With Hypokalaemic Periodic Paralysis and Calcium Channel Mutation
Aktuelle Neurologie
Neurology
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Myotonia in a Patient With a Mutation in an S4 Arginine Residue Associated With Hypokalaemic Periodic Paralysis and a Concomitant Synonymous CLCN1 Mutation
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Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene
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Mutation Analysis of CACNA1S and SCN4A in Patients With Hypokalemic Periodic Paralysis
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