Medium‐chain and long‐chain acyl CoA dehydrogenase deficiency: Clinical, pathologic and ultrastructural differentiation from Reye's syndrome

Hepatology

Volumn 6, Issue 6, 1986, Pages 1270-1278

  Treem, William R ^a,b   Witzleben, Camillus A ^a,b   Piccoli, David A ^a,b   Stanley, Charles A ^a,b   Hale, Daniel E ^a,b   Coates, Paul M ^a,b   Watkins, John B ^a,b  

^a GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL COENZYME A DEHYDROGENASE DEFICIENCY; CASE REPORT; DIAGNOSIS; ELECTRON MICROSCOPY; HUMAN; LIVER; LONG CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; PRIORITY JOURNAL; REYE SYNDROME;

ACYL COENZYME A; ACYL-COA DEHYDROGENASE, LONG-CHAIN; BIOPSY; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INFANT; LIPID METABOLISM, INBORN ERRORS; LIVER; MALE; MICROSCOPY, ELECTRON; MITOCHONDRIA, LIVER; REYE SYNDROME;

EID: 0022996369     PISSN: 02709139     EISSN: 15273350     Source Type: Journal    
DOI: 10.1002/hep.1840060608     Document Type: Article

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