Literature DB >> 3065596

The periodic paralyses.

J E Riggs1.   

Abstract

Patient history and examination often provide sufficient diagnostic clues to allow appropriate classification of the patient with one of the primary periodic paralyses. This article reviews these disorders, their treatment, and the use of provocative testing in their diagnosis. Dysfunction of the muscle membrane sodium channel may be a "final common pathway" pathogenetic mechanism for many of the periodic paralyses.

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Year:  1988        PMID: 3065596

Source DB:  PubMed          Journal:  Neurol Clin        ISSN: 0733-8619            Impact factor:   3.806


  5 in total

1.  Thyrotoxic hypokalemic periodic paralysis in a Hispanic male.

Authors:  Lawrence A Zumo; Christian Terzian; Timothy Brannan
Journal:  J Natl Med Assoc       Date:  2002-05       Impact factor: 1.798

2.  Muscle pathology correlates with permanent weakness in hypokalemic periodic paralysis: a case report.

Authors:  R Gold; H Reichmann
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

3.  Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Authors:  L J Ptacek; F Tyler; J S Trimmer; W S Agnew; M Leppert
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

4.  Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Authors:  L J Ptacek; J S Trimmer; W S Agnew; J W Roberts; J H Petajan; M Leppert
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

5.  Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker.

Authors:  L J Hayward; R H Brown; S C Cannon
Journal:  J Gen Physiol       Date:  1996-05       Impact factor: 4.086

  5 in total

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