98 related articles for article (PubMed ID: 8211942)
1. [Sudden and unexpected death in a young child. 'Crib death' in an older child].
Wierenga H; Smit GP
Tijdschr Kindergeneeskd; 1993 Jun; 61(3):93-6. PubMed ID: 8211942
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Delayed diagnosis of fatal medium-chain acyl-CoA dehydrogenase deficiency in a child.
Shetty AK; Craver RD; Harris JA; Schmidt-Sommerfeld E
Pediatr Emerg Care; 1999 Dec; 15(6):399-401. PubMed ID: 10608324
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Retrospective diagnosis of medium chain acyl-CoA dehydrogenase deficiency.
Christodoulou J; Clarke JT; Rupar CA; Gordon BA; Kelly DP
J Paediatr Child Health; 1993 Jun; 29(3):237-8. PubMed ID: 8518011
[TBL] [Abstract][Full Text] [Related]
9. A neonatal death due to medium-chain acyl-CoA dehydrogenase deficiency: utilization of the neonatal metabolic screen in a functional approach to sudden unexplained infant death.
Manoukian AA; Ha CE; Seaver LH; Bhagavan NV
Am J Forensic Med Pathol; 2009 Sep; 30(3):284-6. PubMed ID: 19696588
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Diagnostic potential of stored dried blood spots for inborn errors of metabolism: a metabolic autopsy of medium-chain acyl-CoA dehydrogenase deficiency.
Kaku N; Ihara K; Hirata Y; Yamada K; Lee S; Kanemasa H; Motomura Y; Baba H; Tanaka T; Sakai Y; Maehara Y; Ohga S
J Clin Pathol; 2018 Oct; 71(10):885-889. PubMed ID: 29720407
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected sibling.
Bennett MJ; Rinaldo P; Millington DS; Tanaka K; Yokota I; Coates PM
Pediatr Pathol; 1991; 11(6):889-95. PubMed ID: 1775402
[TBL] [Abstract][Full Text] [Related]
14. Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementation.
Duran M; Cleutjens CB; Ketting D; Dorland L; de Klerk JB; van Sprang FJ; Berger R
Pediatr Res; 1992 Jan; 31(1):39-42. PubMed ID: 1594328
[TBL] [Abstract][Full Text] [Related]
15. [Deficiency of the fatty-acid oxidising enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in an adult, detected during a neonatal screening programme].
Derks TG; Jakobs H; Gerding A; Niezen-Koning KE; Reijngoud DJ; Smit GP
Ned Tijdschr Geneeskd; 2004 Oct; 148(44):2185-90. PubMed ID: 15559414
[TBL] [Abstract][Full Text] [Related]
16. The Brugada ECG pattern in a neonate.
Sanatani S; Mahkseed N; Vallance H; Brugada R
J Cardiovasc Electrophysiol; 2005 Mar; 16(3):342-4. PubMed ID: 15817096
[TBL] [Abstract][Full Text] [Related]
17. Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.
Yang BZ; Ding JH; Zhou C; Dimachkie MM; Sweetman L; Dasouki MJ; Wilkinson J; Roe CR
Mol Genet Metab; 2000 Mar; 69(3):259-62. PubMed ID: 10767181
[TBL] [Abstract][Full Text] [Related]
18. Medium-chain acyl-CoA dehydrogenase deficiency: a useful diagnosis five years after death.
Bennett MJ; Pollitt RJ; Taitz LS; Variend S
Clin Chem; 1990 Sep; 36(9):1695-7. PubMed ID: 2208722
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
