127 related articles for article (PubMed ID: 1635678)
1. 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]
2. 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]
3. 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]
4. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
Duran M; Hofkamp M; Rhead WJ; Saudubray JM; Wadman SK
Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. MCAD deficiency: what family physicians need to know.
Siwek J
Am Fam Physician; 1989 May; 39(5):116, 119. PubMed ID: 2718890
[No Abstract] [Full Text] [Related]
8. Medium-chain acyl-CoA dehydrogenase deficiency.
Egidio RJ; Francis GL; Coates PM; Hale DE; Roesel A
Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899
[TBL] [Abstract][Full Text] [Related]
9. Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency.
Taubman B; Hale DE; Kelley RI
Pediatrics; 1987 Mar; 79(3):382-5. PubMed ID: 3822638
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency.
Harpey JP; Charpentier C; Coudé M; Divry P; Paturneau-Jouas M
J Pediatr; 1987 Jun; 110(6):881-4. PubMed ID: 3585604
[No Abstract] [Full Text] [Related]
12. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency].
Collet JP; Divry P; Blanc JF; Guibaud P; David M; Macabeo V; Vibert J; Hermier M
Pediatrie; 1984 Dec; 39(8):661-8. PubMed ID: 6535973
[TBL] [Abstract][Full Text] [Related]
13. Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.
Reichmann H; Scheel H; Bier B; Ketelsen UP; Zabransky S
Ann Neurol; 1992 Jan; 31(1):107-9. PubMed ID: 1311909
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Hyperuricemia as the main symptom of medium-chain acyl-Co-A dehydrogenase deficiency].
Reinehr T; Bürk G; Dietz B; Schlüter B; Andler W
Klin Padiatr; 1997; 209(6):357-60. PubMed ID: 9445919
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Medium chain acyl coenzyme A dehydrogenase (MCAD) deficiency: the case for screening all newborns.
Alluri VN; Mulvihill JJ
J Okla State Med Assoc; 2002 May; 95(5):326-8. PubMed ID: 12043106
[TBL] [Abstract][Full Text] [Related]
18. Multiple acyl-coenzyme A dehydrogenase deficiency: diagnosis by acyl-carnitine analysis of a 12-year-old newborn screening card.
Poplawski NK; Ranieri E; Harrison JR; Fletcher JM
J Pediatr; 1999 Jun; 134(6):764-6. PubMed ID: 10356148
[TBL] [Abstract][Full Text] [Related]
19. Inherited metabolic diseases in the sudden infant death syndrome.
Smith LJ
Arch Dis Child; 1992 May; 67(5):662-3. PubMed ID: 1599313
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
