117 related articles for article (PubMed ID: 9059968)
21. [Clinical protocols concerned with disorders of fatty acid beta oxidation].
Kania M
Przegl Lek; 1994; 51(1):25-8. PubMed ID: 8208992
[TBL] [Abstract][Full Text] [Related]
22. Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria.
Elpeleg ON; Christensen E; Hurvitz H; Branski D
Eur J Pediatr; 1990 Jul; 149(10):709-12. PubMed ID: 2120061
[TBL] [Abstract][Full Text] [Related]
23. [Mitochondrial beta-oxidation defects: overview].
Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):60-4. PubMed ID: 11596451
[No Abstract] [Full Text] [Related]
24. Eating disorder in a 6-year-old Asian girl with ethyl malonic adipic aciduria.
Ballard CG; Handy S; McGibben L; Mohan RN; Silveira WR
Int J Eat Disord; 1993 Mar; 13(2):245-8. PubMed ID: 8477295
[TBL] [Abstract][Full Text] [Related]
25. Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome.
Søvik O; Njølstad PR; Jellum E; Molven A
J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S293-7. PubMed ID: 18500571
[TBL] [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. [Hydroxy-methyl-glutaryl-coenzyme A lyase deficiency manifesting as Reye's syndrome in a 3-year-old girl].
Karcher C; Rousselot JM; Lefebvre E; Vidailhet M
Pediatrie; 1993; 48(5):385-7. PubMed ID: 7777393
[TBL] [Abstract][Full Text] [Related]
28. [Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].
Liang Y; Liu L; Wei H; Luo XP; Wang MT
Zhonghua Er Ke Za Zhi; 2003 Dec; 41(12):916-20. PubMed ID: 14723814
[TBL] [Abstract][Full Text] [Related]
29. Reye's syndrome in the United States from 1981 through 1997.
Belay ED; Bresee JS; Holman RC; Khan AS; Shahriari A; Schonberger LB
N Engl J Med; 1999 May; 340(18):1377-82. PubMed ID: 10228187
[TBL] [Abstract][Full Text] [Related]
30. [Myopathies caused by defects of lipid and carbohydrate metabolism].
Angelini C; Martinuzzi A; Micaglio G; Vergani L
Riv Neurol; 1988; 58(1):15-25. PubMed ID: 3047844
[No Abstract] [Full Text] [Related]
31. Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy.
Ozand PT; Rashed M; Millington DS; Sakati N; Hazzaa S; Rahbeeni Z; al Odaib A; Youssef N; Mazrou A; Gascon GG
Brain Dev; 1994 Nov; 16 Suppl():12-22. PubMed ID: 7726376
[TBL] [Abstract][Full Text] [Related]
32. Muscle symptoms and fat oxidation.
Lancet; 1970 May; 1(7656):1096. PubMed ID: 4191970
[No Abstract] [Full Text] [Related]
33. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome].
Brus F; Smit GP; Knoester H; Reijngoud DJ
Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055
[TBL] [Abstract][Full Text] [Related]
34. Is aspirin a cause of Reye's syndrome? A case against.
Orlowski JP; Hanhan UA; Fiallos MR
Drug Saf; 2002; 25(4):225-31. PubMed ID: 11994026
[TBL] [Abstract][Full Text] [Related]
35. Myopathies caused by disorders of lipid metabolism.
Carroll JE
Neurol Clin; 1988 Aug; 6(3):563-74. PubMed ID: 3065601
[TBL] [Abstract][Full Text] [Related]
36. [Reye's syndrome. Description of a case focused on the patient's epileptic seizures].
Jiménez-Caballero PE; Montes-Gonzalo MC; Velázquez-Pérez JM
Rev Neurol; 2008 Dec 1-15; 47(11):571-4. PubMed ID: 19048536
[TBL] [Abstract][Full Text] [Related]
37. Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases.
Mantagos S; Genel M; Tanaka K
J Clin Invest; 1979 Dec; 64(6):1580-9. PubMed ID: 500826
[TBL] [Abstract][Full Text] [Related]
38. Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.
Bell RB; Brownell AK; Roe CR; Engel AG; Goodman SI; Frerman FE; Seccombe DW; Snyder FF
Neurology; 1990 Nov; 40(11):1779-82. PubMed ID: 2234436
[TBL] [Abstract][Full Text] [Related]
39. Clinical manifestations and management of fatty acid oxidation disorders.
Merritt JL; MacLeod E; Jurecka A; Hainline B
Rev Endocr Metab Disord; 2020 Dec; 21(4):479-493. PubMed ID: 32654032
[TBL] [Abstract][Full Text] [Related]
40. Severe infantile hypotonia with ethylmalonic aciduria: case report.
Okuyaz C; Ezgü FS; Biberoglu G; Zeviani M; Tiranti V; Yilgör E
J Child Neurol; 2008 Jun; 23(6):703-5. PubMed ID: 18539996
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
