112 related articles for article (PubMed ID: 1537363)
21. Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency.
Bertini E; Dionisi-Vici C; Garavaglia B; Burlina AB; Sabatelli M; Rimoldi M; Bartuli A; Sabetta G; DiDonato S
Eur J Pediatr; 1992 Feb; 151(2):121-6. PubMed ID: 1537353
[TBL] [Abstract][Full Text] [Related]
22. Riboflavin responsive multiple acyl-CoA dehydrogenation deficiency. Assessment of 3 years of riboflavin treatment.
Gregersen N; Christensen MF; Christensen E; Kølvraa S
Acta Paediatr Scand; 1986 Jul; 75(4):676-81. PubMed ID: 3751563
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Reye syndrome and reye-like syndrome.
Gosalakkal JA; Kamoji V
Pediatr Neurol; 2008 Sep; 39(3):198-200. PubMed ID: 18725066
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern.
Rowe PC; Valle D; Brusilow SW
JAMA; 1988 Dec; 260(21):3167-70. PubMed ID: 3184395
[TBL] [Abstract][Full Text] [Related]
27. [Acute encephalopathy and recurrent hepatic steatosis with normal long and medium chain fatty acyl-CoA-dehydrogenase activity].
Marandian MH; Soltanabadi A; Rakchan M; Kouchanfar A; Fallah A
Arch Fr Pediatr; 1987 May; 44(5):369-71. PubMed ID: 3619569
[TBL] [Abstract][Full Text] [Related]
28. Sudden infant death and lysinuric protein intolerance.
de Klerk JB; Duran M; Huijmans JG; Mancini GM
Eur J Pediatr; 1996 Mar; 155(3):256-7. PubMed ID: 8929742
[No Abstract] [Full Text] [Related]
29. Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management.
Sluysmans T; Tuerlinckx D; Hubinont C; Verellen-Dumoulin C; Brivet M; Vianey-Saban C
J Pediatr; 1997 Sep; 131(3):444-6. PubMed ID: 9329424
[TBL] [Abstract][Full Text] [Related]
30. Mouse models for disorders of mitochondrial fatty acid beta-oxidation.
Schuler AM; Wood PA
ILAR J; 2002; 43(2):57-65. PubMed ID: 11917157
[TBL] [Abstract][Full Text] [Related]
31. Sudden infant death and multiple acyl-CoA dehydrogenation disorders.
Parini R; Vegni C; Martini J; Romeo A; Garavaglia B
Eur J Pediatr; 1995 May; 154(5):421-2. PubMed ID: 7641783
[No Abstract] [Full Text] [Related]
32. Differential diagnosis of Reye's syndrome.
Allison F; Bennett MJ
Dev Med Child Neurol; 1987 Dec; 29(6):830. PubMed ID: 3691984
[No Abstract] [Full Text] [Related]
33. [Very-long-chain acyl-CoA dehydrogenase deficiency].
Uchiyama A; Takusa Y; Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):65-7. PubMed ID: 11596452
[No Abstract] [Full Text] [Related]
34. Metabolic cause of Reye-like syndrome.
Bzduch V; Behulova D; Lehnert W; Fabriciova K; Kozak L; Salingova A; Hrabincova E; Benedekova M
Bratisl Lek Listy; 2001; 102(9):427-9. PubMed ID: 11763681
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. [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]
37. 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]
38. A rapid MRI technique for the assessment of hepatic steatosis in a subject with medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency.
Fishbein M; Smith M; Li BU
J Pediatr Gastroenterol Nutr; 1998 Aug; 27(2):224-7. PubMed ID: 9702659
[No Abstract] [Full Text] [Related]
39. One more thought on sudden infant death syndrome.
Albers S; Levy HL
Pediatrics; 2001 Apr; 107(4):809. PubMed ID: 11380009
[No Abstract] [Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
