Gender differences in penetrance and phenotype in hypokalemic periodic paralysis

A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis

(2011) Makito Hirano et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

(2011) E. Matthews et al.   NEUROLOGY

Leaky sodium channels from voltage sensor mutations in periodic paralysis, but not paramyotonia

(2011) D. G. Francis et al.   NEUROLOGY

Recent Advances in the Pathogenesis and Drug Action in Periodic Paralyses and Related Channelopathies

(2011) Domenico Tricarico et al.   Frontiers in Pharmacology

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family

(2009) Tie Ke et al.   JOURNAL OF HUMAN GENETICS

Disappearance of Episodic Weakness During Pregnancy in Hyperkalemic Periodic Paralysis From the SCNA4 Mutation T704M

(2009) Josef Finsterer   NEUROLOGIST

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

(2009) E. Matthews et al.   NEUROLOGY

Gating Pore Currents in DIIS4 Mutations of NaV1.4 Associated with Periodic Paralysis: Saturation of Ion Flux and Implications for Disease Pathogenesis

(2008) Arie F. Struyk et al.   JOURNAL OF GENERAL PHYSIOLOGY

Gender Differences in Clinical Manifestations of Brugada Syndrome

(2008) Begoña Benito et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita

(2008) Doreen Fialho et al.   NEUROMUSCULAR DISORDERS