188 related articles for article (PubMed ID: 1962058)
1. Deficiency of the pyruvate dehydrogenase complex and of mitochondrial fatty acid oxidation.
Bindoff LA; Birch-Machin MA; Jackson S; Singh Kler R; Bartlett K; Turnbull DM
Rev Neurol (Paris); 1991; 147(6-7):526-31. PubMed ID: 1962058
[TBL] [Abstract][Full Text] [Related]
2. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
Stanley CA
Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304
[TBL] [Abstract][Full Text] [Related]
3. Diagnosis of mitochondrial fatty acid oxidation defects.
Duran M; Bruinvis L; Ketting D; Dorland L
Padiatr Padol; 1993; 28(1):19-25. PubMed ID: 8446424
[TBL] [Abstract][Full Text] [Related]
4. Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death.
Pollitt RJ
Padiatr Padol; 1993; 28(1):13-7. PubMed ID: 8446423
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
Gregersen N; Andresen BS; Corydon MJ; Corydon TJ; Olsen RK; Bolund L; Bross P
Hum Mutat; 2001 Sep; 18(3):169-89. PubMed ID: 11524729
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial fatty-acid oxidation disorders.
Kompare M; Rizzo WB
Semin Pediatr Neurol; 2008 Sep; 15(3):140-9. PubMed ID: 18708005
[TBL] [Abstract][Full Text] [Related]
7. Intestinal pseudo-obstruction as a manifestation of impaired mitochondrial fatty acid oxidation.
Gilbert J; Ibdah JA
Med Hypotheses; 2005; 64(3):586-9. PubMed ID: 15617873
[TBL] [Abstract][Full Text] [Related]
8. Magnetic resonance spectroscopic investigation of mitochondrial fuel metabolism and energetics in cultured human fibroblasts: effects of pyruvate dehydrogenase complex deficiency and dichloroacetate.
Simpson NE; Han Z; Berendzen KM; Sweeney CA; Oca-Cossio JA; Constantinidis I; Stacpoole PW
Mol Genet Metab; 2006; 89(1-2):97-105. PubMed ID: 16765624
[TBL] [Abstract][Full Text] [Related]
9. [Hepatic mitochondrial fatty acid oxidation disorders].
Matsubara Y
Ryoikibetsu Shokogun Shirizu; 1995; (8):312-6. PubMed ID: 8581639
[No Abstract] [Full Text] [Related]
10. Defects in long chain fatty acid oxidation presenting as severe cardiomyopathy and cardiogenic shock in infancy.
Dereddy NR; Kronn D; Krishnan U
Cardiol Young; 2009 Sep; 19(5):540-2. PubMed ID: 19691901
[TBL] [Abstract][Full Text] [Related]
11. [Mitochondrial beta-oxidation defects].
Woldseth B; Rootwelt T
Tidsskr Nor Laegeforen; 2006 Mar; 126(6):756-9. PubMed ID: 16541168
[TBL] [Abstract][Full Text] [Related]
12. [Mitochondrial beta-oxidation defects: overview].
Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):60-4. PubMed ID: 11596451
[No Abstract] [Full Text] [Related]
13. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Treem WR; Rinaldo P; Hale DE; Stanley CA; Millington DS; Hyams JS; Jackson S; Turnbull DM
Hepatology; 1994 Feb; 19(2):339-45. PubMed ID: 8294091
[TBL] [Abstract][Full Text] [Related]
14. Inherited disorders of mitochondrial fatty acid oxidation: a new responsibility for the neonatologist.
Roe CR
Semin Neonatol; 2002 Feb; 7(1):37-47. PubMed ID: 12069537
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial fatty acid oxidation disorders and cyclic vomiting syndrome.
Rinaldo P
Dig Dis Sci; 1999 Aug; 44(8 Suppl):97S-102S. PubMed ID: 10490047
[TBL] [Abstract][Full Text] [Related]
16. In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: limited diagnostic use of 1-13C fatty acid breath test using bolus technique.
Jakobs C; Kneer J; Martin D; Boulloche J; Brivet M; Poll-The BT; Saudubray JM
Eur J Pediatr; 1997 Aug; 156 Suppl 1():S78-82. PubMed ID: 9266222
[TBL] [Abstract][Full Text] [Related]
17. A case of impairment of mitochondrial fatty acid beta-oxidation.
Hasegawa T; Hori N; Du W
Keio J Med; 2002 Jun; 51(2):100-6. PubMed ID: 12125906
[TBL] [Abstract][Full Text] [Related]
18. Fatty acid transport and mitochondrial oxidation disorders.
Rinaldo P
Semin Liver Dis; 2001 Nov; 21(4):489-500. PubMed ID: 11745037
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Myopathies with miscellaneous disorders related to mitochondrial fatty acid oxidation: defective synthesis of ketone body, long-chain fatty acid transport defect, and muscular coenzyme Q10 deficiency].
Takusa Y; Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):90-4. PubMed ID: 11596461
[No Abstract] [Full Text] [Related]
[Next] [New Search]