141 related articles for article (PubMed ID: 7720752)
1. Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?
Opdal SH; Vege A; Saugstad OD; Rognum TO
Eur J Pediatr; 1995 Feb; 154(2):166-7. PubMed ID: 7720752
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.
Kelly DP; Whelan AJ; Hale DE; Rinaldo P; Rutledge SL; Zhang Z; Strauss AW
Prog Clin Biol Res; 1992; 375():463-72. PubMed ID: 1438388
[No Abstract] [Full Text] [Related]
6. The prevalence of the G985 allele of medium-chain acyl-CoA dehydrogenase deficiency among sudden infant death victims and healthy newborns in northern Germany.
Santer R; Gregersen N; Tanaka K; Hinck-Kneip C; Krawinkel M; Schaub J
Eur J Pediatr; 1995 Jun; 154(6):497. PubMed ID: 7671949
[No Abstract] [Full Text] [Related]
7. A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).
Andresen BS; Bross P; Jensen TG; Winter V; Knudsen I; Kølvraa S; Jensen UB; Bolund L; Duran M; Kim JJ
Am J Hum Genet; 1993 Sep; 53(3):730-9. PubMed ID: 8102510
[TBL] [Abstract][Full Text] [Related]
8. The frequency of medium-chain acyl-CoA dehydrogenase G985 mutation in the Hungarian population.
Szalai C; Czinner A; Revai K
Eur J Pediatr; 1996 Mar; 155(3):256. PubMed ID: 8929741
[No Abstract] [Full Text] [Related]
9. 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]
10. A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.
Brackett JC; Sims HF; Steiner RD; Nunge M; Zimmerman EM; deMartinville B; Rinaldo P; Slaugh R; Strauss AW
J Clin Invest; 1994 Oct; 94(4):1477-83. PubMed ID: 7929823
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Is genotyping useful for the screening of medium-chain acyl-CoA dehydrogenase deficiency in France?
Ged C; el Sebai H; de Verneuil H; Parrot-Rouleau F
J Inherit Metab Dis; 1995; 18(2):253-6. PubMed ID: 7564261
[No 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. 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]
15. Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death.
Kelly DP; Hale DE; Rutledge SL; Ogden ML; Whelan AJ; Zhang Z; Strauss AW
J Inherit Metab Dis; 1992; 15(2):171-80. PubMed ID: 1356169
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
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. Is the G985A allelic variant of medium-chain acyl-CoA dehydrogenase a risk factor for sudden infant death syndrome? A pooled analysis.
Wang SS; Fernhoff PM; Khoury MJ
Pediatrics; 2000 May; 105(5):1175-6. PubMed ID: 10836898
[No Abstract] [Full Text] [Related]
20. Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene.
Gregersen N; Blakemore AI; Winter V; Andresen B; Kølvraa S; Bolund L; Curtis D; Engel PC
Clin Chim Acta; 1991 Nov; 203(1):23-34. PubMed ID: 1769118
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
