Sudden death beyond sids

Fetal and Pediatric Pathology

Volumn 16, Issue 4, 1996, Pages 691-693

  Boles, Richard G ^a   Boesel, Carl ^b   Rinaldo, Piero ^c  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b NATIONWIDE CHILDREN S HOSPITAL   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; ACYL COENZYME A DESATURASE;

ADOLESCENT; AGE; CASE REPORT; FATALITY; FEMALE; HUMAN; INFANT; LETTER; PATHOLOGY; SUDDEN INFANT DEATH SYNDROME;

ACYL-COA DEHYDROGENASE; ADOLESCENT; AGE FACTORS; FATAL OUTCOME; FATTY ACID DESATURASES; FEMALE; HUMANS; INFANT; SUDDEN INFANT DEATH;

EID: 0030178711     PISSN: 15513815     EISSN: 15513823     Source Type: Journal    
DOI: 10.1080/15513819609168705     Document Type: Letter

References (5)

1. Ziadeh R, Hoffman EP, Finegold DN, et al. Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: Neonatal screening shows high incidence and unexpected mutation frequencies. Pediatr Res 1995;37:675-8.
2. Roe CR, Coates PM. Mitochondrial fatty acid oxidation disorders. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. 7th ed. New York: McGraw-Hill, 1995,1501-33.
3. Boles RG, Martin SK, Blitzer MG, Rinaldo P. Biochemical diagnosis of fatly acid oxidation disorders by metabolite analysis of posunortem liver. Hum Pathol 1994;25:735-41. (Pubitemid 24249229)
4. Rinaldo P, O'Shea JJ, Coates PM, Hale DE, Stanley CA, Tanaka K. Medium chain acyl-CoA dehydrogenase deficiency: Diagnosis by stable isotope dilution analysis of urinary n-hexanoylglycine and 3-phenylpropionylglycine. N Engl J Med 1988;319:1308-13. (Pubitemid 19003392)
5. Thomas J, Greene C. The underascertainment of medium chain acyl-CoA dehydrogenase deficiency (MCADD). In: Annual Meeting of the Society of Inherited Metabolic Disorders, Orange Beach, Alabama, 18-21 March 1995. Abstract 5.