Persistent hypoglycemia associated with lipid storage myopathy in a paint foal

Author:

Pinn Toby L.1,Divers Thomas J.1ORCID,Southard Teresa2,De Bernardis Nikhita P.3ORCID,Wakshlag Joe J.1,Valberg Stephanie4ORCID

Affiliation:

1. Department of Clinical Sciences; Cornell University College of Veterinary Medicine; Ithaca New York

2. Department of Biomedical Sciences, Cornell University College of Veterinary Medicine; Ithaca New York

3. Veterinary Practice; Boyds Maryland

4. Department of Large Animal Clinical Sciences; Michigan State University; East Lansing Michigan

Publisher

Wiley

Subject

General Veterinary

Reference21 articles.

1. Development of a scoring system for the early diagnosis of equine neonatal sepsis;Brewer;Equine Vet J.,1988

2. Genetic mapping of GBE1 and its association with glycogen storage disease IV in American Quarter horses;Ward;Cytogenet Genome Res.,2003

3. Equine multiple acyl-CoA dehydrogenase deficiency (MADD) associated with seasonal pasture myopathy in the midwestern United States;Sponseller;J Vet Intern Med.,2012

4. Diagnosis of mitochondrial fatty acid oxidation defects;Duran;Padiatr Padol.,1993

5. Lipid storage myopathy;Liang;Curr Neurol Neurosci Rep.,2011

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1. Laboratory Assessment of Lipid and Glucose Metabolism;Equine Hematology, Cytology, and Clinical Chemistry;2020-11-20

2. Laboratory Markers of Muscle Injury;Equine Hematology, Cytology, and Clinical Chemistry;2020-11-20

3. Detection of hypoglycin A and MCPA‐carnitine in equine serum and muscle tissue: Optimisation and validation of a LC‐MS–based method without derivatisation;Equine Veterinary Journal;2020-08-12

4. Genetics of Equine Muscle Disease;Veterinary Clinics of North America: Equine Practice;2020-08

5. Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study;Medical Science Monitor;2019-11-30

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