139 related articles for article (PubMed ID: 8496748)
1. Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome.
Arens R; Gozal D; Jain K; Muscati S; Heuser ET; Williams JC; Keens TG; Ward SL
J Pediatr; 1993 May; 122(5 Pt 1):715-8. PubMed ID: 8496748
[TBL] [Abstract][Full Text] [Related]
2. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS).
Miller M; Brooks J; Forbes N; Insel R
Prog Clin Biol Res; 1992; 375():495-8. PubMed ID: 1438393
[No Abstract] [Full Text] [Related]
3. Frequency of medium-chain acyl-CoA dehydrogenase deficiency G-985 mutation in sudden infant death syndrome.
Miller ME; Brooks JG; Forbes N; Insel R
Pediatr Res; 1992 Apr; 31(4 Pt 1):305-7. PubMed ID: 1570195
[TBL] [Abstract][Full Text] [Related]
4. Scottish frequency of the common G985 mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS).
Dundar M; Lanyon WG; Connor JM
J Inherit Metab Dis; 1993; 16(6):991-3. PubMed ID: 8127075
[TBL] [Abstract][Full Text] [Related]
5. Medium-chain acyl-CoA dehydrogenase deficiency does not correlate with apparent life-threatening events and the sudden infant death syndrome: results from phenylpropionate loading tests and DNA analysis.
Penzien JM; Molz G; Wiesmann UN; Colombo JP; Bühlmann R; Wermuth B
Eur J Pediatr; 1994 May; 153(5):352-7. PubMed ID: 8033926
[TBL] [Abstract][Full Text] [Related]
6. Medium chain acyl-coenzyme A dehydrogenase deficiency and SIDS.
Hegyi T; Ostfeld B; Gardner K
N J Med; 1992 May; 89(5):385-92. PubMed ID: 1635678
[TBL] [Abstract][Full Text] [Related]
7. [Screening of A985 to G mutation of medium-chain acyl-CoA dehydrogenase (MCAD) gene in Normandy. Evaluation of the role of MCAD deficiency in sudden infant death].
Lecoq I; Mallet E; Bonté JB; Laroche D; Travert G
C R Seances Soc Biol Fil; 1995; 189(2):295-301. PubMed ID: 8590228
[TBL] [Abstract][Full Text] [Related]
8. The sudden infant death syndrome gene: does it exist?
Opdal SH; Rognum TO
Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
[TBL] [Abstract][Full Text] [Related]
9. Rapid testing for the MCAD G583A mutation, by PCR-mediated site directed mutagenesis, in an Australian population of SIDS patients.
Ryan A; McGill J; Mountain H
Dis Markers; 1997 Apr; 13(2):131-4. PubMed ID: 9160189
[TBL] [Abstract][Full Text] [Related]
10. Medium chain acyl-coenzyme A dehydrogenase deficiency.
Bennett MJ; Hale DE
N J Med; 1992 Sep; 89(9):675-8. PubMed ID: 1436730
[TBL] [Abstract][Full Text] [Related]
11. Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death.
Ding JH; Roe CR; Iafolla AK; Chen YT
N Engl J Med; 1991 Jul; 325(1):61-2. PubMed ID: 2046713
[No Abstract] [Full Text] [Related]
12. Inherited metabolic diseases in the sudden infant death syndrome.
Holton JB; Allen JT; Green CA; Partington S; Gilbert RE; Berry PJ
Arch Dis Child; 1991 Nov; 66(11):1315-7. PubMed ID: 1755645
[TBL] [Abstract][Full Text] [Related]
13. Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency.
Andresen BS; Bross P; Jensen TG; Knudsen I; Winter V; Kølvraa S; Bolund L; Gregersen N
Scand J Clin Lab Invest Suppl; 1995; 220():9-25. PubMed ID: 7652482
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood.
Gregersen N; Winter V; Jensen PK; Holmskov A; Kølvraa S; Andresen BS; Christensen E; Bross P; Lundemose JB; Gregersen M
Prenat Diagn; 1995 Jan; 15(1):82-6. PubMed ID: 7740006
[TBL] [Abstract][Full Text] [Related]
15. The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndrome.
Lundemose JB; Gregersen N; Kølvraa S; Nørgaard Pedersen B; Gregersen M; Helweg-Larsen K; Simonsen J
Acta Paediatr; 1993; 82(6-7):544-6. PubMed ID: 8338987
[TBL] [Abstract][Full Text] [Related]
16. Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency.
Kemp PM; Little BB; Bost RO; Dawson DB
Am J Forensic Med Pathol; 1996 Mar; 17(1):79-82. PubMed ID: 8838477
[TBL] [Abstract][Full Text] [Related]
17. Comment on "Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency".
Ross KF; Guileyardo JM; Bennett MJ; Barnard JJ
Am J Forensic Med Pathol; 1996 Dec; 17(4):349-50. PubMed ID: 8947364
[No Abstract] [Full Text] [Related]
18. Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years.
Lundemose JB; Kølvraa S; Gregersen N; Christensen E; Gregersen M
Mol Pathol; 1997 Aug; 50(4):212-7. PubMed ID: 9350306
[TBL] [Abstract][Full Text] [Related]
19. The A985 to G mutation of the medium-chain acyl-CoA dehydrogenase gene and sudden infant death syndrome in Normandy.
Lecoq I; Mallet E; Bonte JB; Travert G
Acta Paediatr; 1996 Feb; 85(2):145-7. PubMed ID: 8640038
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome.
Howat AJ; Bennett MJ; Variend S; Shaw L
Br Med J (Clin Res Ed); 1984 Mar; 288(6422):976. PubMed ID: 6423169
[No Abstract] [Full Text] [Related]
[Next] [New Search]