Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy-Reference-Cited by-同舟云学术

Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy

Published:2008-05 Issue:5 Volume:18 Page:355-364
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Westermann C.M.,Dorland L.,Votion D.M.,de Sain-van der Velden M.G.M.,Wijnberg I.D.,Wanders R.J.A.,Spliet W.G.M.,Testerink N.,Berger R.,Ruiter J.P.N.,van der Kolk J.H.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference21 articles.

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2. Morphological alterations in oxidative muscles and mitochondrial structure associated with equine atypical myopathy;Cassart;Equine Vet J,2007

3. Atypical myoglobinuria: an acute myopathy in grazing horses;Whitwell;Equine Vet J,1988

4. Myoglobinuria in horses;Bowen;Vet Rec,1942

5. Seasonal pasture myopathy in horses in the midwestern United States: 14 cases (1998–2005);Finno;J Am Vet Med Assoc,2006

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