Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition-Reference-Cited by-同舟云学术

Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition

Published:1999-03 Issue:2 Volume:31 Page:153-159
ISSN:0425-1644
Container-title:Equine Veterinary Journal
language:en
Short-container-title:

Author:

NAYLOR J. M.,NICKEL D. D.,TRIMINO G.,CARD C.,LIGHTFOOT K.,ADAMS G.

Publisher

Wiley

Subject

General Medicine

Reference22 articles.

1. Laryngeal and pharyngeal dysfunction in horses homozygous for hyperkalaemic periodic paralysis;Carr;J. Am. vet. med. Ass.,1996

2. Hyperkalaemic periodic paralysis in Australian Quarter Horses;Church;Aust. Vet. J.,1995

3. Hyperthermia during isoflurane anaesthesia in a horse with suspected hyperkalaemic periodic paralysis;Cornick;Equine vet. J.,1994

4. An episodic weakness in four horses associated with intermittent serum hyperkalaemia and the similarity of the disease to hyperkalaemic periodic paresis in man;Cox;Proc. Am. Ass. equine Practitnrs.,1986

5. Laryngospasm, dysphagia, and emaciation associated with hyperkalaemic periodic paralysis in a horse;Guglick;J. Am. vet. med. Ass.,1996

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