Diagnosis of occult muscular dystrophy: Importance of the “chance” finding of elevated serum aminotransferase activities

Journal of Pediatrics

Volumn 122, Issue 2, 1993, Pages 254-256

  Morse, Richard P ^a   Rosman, N Paul ^a  

^a FLOATING HOSPITAL FOR CHILDREN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOTRANSFERASE; CREATINE KINASE;

ARTICLE; CASE REPORT; CHILD; CLINICAL ARTICLE; ENZYME ACTIVITY; FEMALE; HUMAN; MALE; MUSCULAR DYSTROPHY; PRIORITY JOURNAL;

EID: 0027458614     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(06)80126-5     Document Type: Article

References (14)

1. Persistent hypertransaminasemia as the presenting finding of childhood muscle disease
2. Prolonged elevation of transaminase concentration in children with unsuspected myopathy
3. Hypertransaminasémie prolongée révélatrice d'une myopathie
4. Persistent elevation of transminases as the presenting finding in an adolescent with an unsuspected muscle glycogenosis
5. The clinical significance of transaminase activities of serum
6. Creatine kinase isoenzyme patterns in human tissue obtained at surgery
7. Aldolase in the serum and tissues of tumor-bearing animals
8. High creatine phosphokinase activity of sera of progressive muscular dystrophy
9. Etude de la créatine-kinase sérique chez les myopathes et leurs familles
10. Diagnostic and prognostic significance of serum enzymes. I. Muscular Dystrophy
11. Serum enzyme alterations in neuromuscular disorders
12. Serum enzymes in muscular dystrophy and certain other muscular and neuromuscular diseases. I. Serum glutamic oxalacetic transaminase
13. Duchenne muscular dystrophy