278 related articles for article (PubMed ID: 9290601)
1. The metabolic crisis: a diagnostic challenge [editoria; comment].
Bove KE
J Pediatr; 1997 Aug; 131(2):181-2. PubMed ID: 9290601
[No Abstract] [Full Text] [Related]
2. [Metabolic crisis in an infant--is the problem in the mitochondria?].
Tyni T; Pihko H
Duodecim; 2002; 118(13):1331-9. PubMed ID: 12239878
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. [Carnitine deficiency in inborn errors of metabolism].
Sela BA; Lerman-Sagie T; Berkovitz M
Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309
[TBL] [Abstract][Full Text] [Related]
6. The fate of orally ingested 3-phenylpropionic acid.
Duran M; van Vossen R; Bruinvis L; Ketting D; Dorland L; de Klerk JB
Prog Clin Biol Res; 1990; 321():419-26. PubMed ID: 2326303
[No Abstract] [Full Text] [Related]
7. 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]
8. MCAD deficiency. Acylcarnitines (AC) by tandem mass spectrometry (MS-MS) are useful to monitor dietary treatment.
Abdenur JE; Chamoles NA; Specola N; Schenone AB; Jorge L; Guinle A; Bernard CI; Levandowskiy V; Lavorgna S
Adv Exp Med Biol; 1999; 466():353-63. PubMed ID: 10709663
[No Abstract] [Full Text] [Related]
9. Medicine. Fast technology drives new world of newborn screening.
Marshall E
Science; 2001 Dec; 294(5550):2272-4. PubMed ID: 11743177
[No Abstract] [Full Text] [Related]
10. Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death.
Roe CR; Millington DS; Maltby DA; Wellman RB
Lancet; 1987 Feb; 1(8531):512. PubMed ID: 2881073
[No Abstract] [Full Text] [Related]
11. Diagnostic tests for acyl-coenzyme A dehydrogenase deficiency.
Elpeleg ON
J Pediatr; 1992 Oct; 121(4):667-8. PubMed ID: 1403411
[No Abstract] [Full Text] [Related]
12. [Medium chain Acyl-Coa Dehydrogenase deficiency. A diagnostic challenge for clinicians and laboratory].
Heinonen OJ; Iitiä A; Irjala K; Pulkki K
Duodecim; 1996; 112(1):35-41. PubMed ID: 10590599
[No Abstract] [Full Text] [Related]
13. Neonatal screening for inborn errors of metabolism.
Morris AA
Indian Pediatr; 2000 Dec; 37(12):1303-6. PubMed ID: 11119331
[No Abstract] [Full Text] [Related]
14. [Application of tandem mass spectrometry on the diagnosis of fatty acid oxidation disorders].
Han LS; Ye J; Qiu WJ; Gao XL; Wang Y; Zhang YJ; Gu XF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):692-5. PubMed ID: 18067086
[TBL] [Abstract][Full Text] [Related]
15. A genetic defect in carnitine transport causing primary carnitine deficiency.
Stanley CA; Treem WR; Hale DE; Coates PM
Prog Clin Biol Res; 1990; 321():457-64. PubMed ID: 2326306
[No Abstract] [Full Text] [Related]
16. Neonatal screening for medium chain acyl-CoA deficiency: high incidence in Lower Saxony (northern Germany).
Sander S; Janzen N; Janetzky B; Scholl S; Steuerwald U; Schäfer J; Sander J
Eur J Pediatr; 2001 May; 160(5):318-9. PubMed ID: 11388605
[No Abstract] [Full Text] [Related]
17. Screening for inherited metabolic disease in newborn infants using tandem mass spectrometry.
Leonard JV; Dezateux C
BMJ; 2002 Jan; 324(7328):4-5. PubMed ID: 11777783
[No Abstract] [Full Text] [Related]
18. Neurological diseases in disorders of organic acids.
Marsden DL; Nyhan WL
Curr Opin Neurol Neurosurg; 1992 Jun; 5(3):349-54. PubMed ID: 1623263
[TBL] [Abstract][Full Text] [Related]
19. The role of tandem mass spectrometry in the diagnosis of fatty acid oxidation disorders.
Millington DS; Terada N; Chace DH; Chen YT; Ding JH; Kodo N; Roe CR
Prog Clin Biol Res; 1992; 375():339-54. PubMed ID: 1438380
[No Abstract] [Full Text] [Related]
20. Public health explores expanding newborn screening for cystic fibrosis, congenital adrenal hyperplasia, and medium-chain acyl coenzyme A dehydrogenase deficiency (MCAD).
Rhoades E; King P
J Okla State Med Assoc; 2001 Apr; 94(4):129-32. PubMed ID: 11392180
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]