Literature DB >> 9106348

Hyperkalemic periodic paralysis.

J M Naylor1.   

Abstract

Hyperkalemic periodic paralysis is an autosomal codominant genetic disease of horses who are descendants of the quarter horse sire Impressive. It produces a muscular phenotype that has been selected by show judges, which has resulted in the rapid dissemination of this disease. Clinical attacks are characterized by muscle fasciculation and spasm, and they respond to treatments for the concurrent hyperkalemia.

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Year:  1997        PMID: 9106348     DOI: 10.1016/s0749-0739(17)30260-2

Source DB:  PubMed          Journal:  Vet Clin North Am Equine Pract        ISSN: 0749-0739            Impact factor:   1.792


  2 in total

1.  A genome-wide association study for harness racing success in the Norwegian-Swedish coldblooded trotter reveals genes for learning and energy metabolism.

Authors:  Brandon D Velie; Kim Jäderkvist Fegraeus; Marina Solé; Maria K Rosengren; Knut H Røed; Carl-Fredrik Ihler; Eric Strand; Gabriella Lindgren
Journal:  BMC Genet       Date:  2018-08-29       Impact factor: 2.797

2.  The effect of oral sodium acetate administration on plasma acetate concentration and acid-base state in horses.

Authors:  Amanda Waller; Michael I Lindinger
Journal:  Acta Vet Scand       Date:  2007-12-20       Impact factor: 1.695

  2 in total

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