Equine biochemical multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of rhabdomyolysis

Molecular Genetics and Metabolism

Volumn 91, Issue 4, 2007, Pages 362-369

  Westermann, C M ^a   de Sain van der Velden, M G M ^b   van der Kolk, J H ^a   Berger, R ^b   Wijnberg, I D ^a   Koeman, J P ^c   Wanders, R J A ^d   Lenstra, J A ^a   Testerink, N ^e   Vaandrager, A B ^e   Vianey Saban, C ^f   Acquaviva Bourdain, C ^f   Dorland, L ^b  

^a Faculty of Veterinary Medicine   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c UTRECHT UNIVERSITY   (Netherlands)

^d ACADEMIC MEDICAL CENTER   (Netherlands)

^e UTRECHT UNIVERSITY   (Netherlands)

^f HÔPITAL DEBROUSSE   (France)

Author keywords

ETF; ETF QO; Horse; MADD; Myopathy; Rhabdomyolysis

Indexed keywords

2 METHYLSUCCINIC ACID; ACYLCARNITINE; ASPARTATE AMINOTRANSFERASE; BUTYRYL COENZYME A DEHYDROGENASE; BUTYRYLGLYCINE ISOVALERYLGLYCINE; CREATINE KINASE; CREATININE; ETHYLMALONIC ACID; GLYCINE DERIVATIVE; HEXANOYLGLYCINE; ISOVALERYL COENZYME A DEHYDROGENASE; LACTATE DEHYDROGENASE; LACTIC ACID; MALONIC ACID; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE; SUCCINIC ACID DERIVATIVE; UNCLASSIFIED DRUG; UREA;

ANIMAL TISSUE; ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; ENZYME DEFICIENCY; GAIT DISORDER; HORSE; HYPERGLYCEMIA; KIDNEY DYSFUNCTION; LACTIC ACIDEMIA; LIPIDOSIS; METABOLIC DISORDER; MULTIPLE ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MYOGLOBINURIA; NONHUMAN; PRIORITY JOURNAL; RHABDOMYOLYSIS;

ACYL-COA DEHYDROGENASE; ANIMALS; FEMALE; HORSE DISEASES; HORSES; MALE; RHABDOMYOLYSIS;

ANIMALIA; EQUIDAE;

EID: 34447276479     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2007.04.010     Document Type: Article

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