These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

87 related articles for article (PubMed ID: 21626870)

  • 1. [Anesthetic management in a patient with trifunctional protein deficiency].
    Makise K; Inagawa G; Ka K
    Masui; 2011 May; 60(5):628-30. PubMed ID: 21626870
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.
    Jackson S; Kler RS; Bartlett K; Pourfarzam M; Aynsley-Green A; Bindoff LA; Turnbull DM
    Prog Clin Biol Res; 1992; 375():327-37. PubMed ID: 1438378
    [No Abstract]   [Full Text] [Related]  

  • 3. Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.
    Kamijo T; Wanders RJ; Saudubray JM; Aoyama T; Komiyama A; Hashimoto T
    J Clin Invest; 1994 Apr; 93(4):1740-7. PubMed ID: 8163672
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Hagenfeldt L; Venizelos N; von Döbeln U
    J Inherit Metab Dis; 1995; 18(2):245-8. PubMed ID: 7564259
    [No Abstract]   [Full Text] [Related]  

  • 5. Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts.
    Roe DS; Yang BZ; Vianey-Saban C; Struys E; Sweetman L; Roe CR
    Mol Genet Metab; 2006 Jan; 87(1):40-7. PubMed ID: 16297647
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype.
    Ijlst L; Uskikubo S; Kamijo T; Hashimoto T; Ruiter JP; de Klerk JB; Wanders RJ
    J Inherit Metab Dis; 1995; 18(2):241-4. PubMed ID: 7564258
    [No Abstract]   [Full Text] [Related]  

  • 7. [Peroxisomal disorders].
    Suzuki Y; Shimozawa N; Imamura A; Kondo N
    Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):452-9. PubMed ID: 11031991
    [No Abstract]   [Full Text] [Related]  

  • 8. [Bifunctional enzyme deficiency].
    Suzuki Y
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):326-7. PubMed ID: 9645073
    [No Abstract]   [Full Text] [Related]  

  • 9. Combined enzyme defect of mitochondrial fatty acid oxidation.
    Jackson S; Kler RS; Bartlett K; Briggs H; Bindoff LA; Pourfarzam M; Gardner-Medwin D; Turnbull DM
    J Clin Invest; 1992 Oct; 90(4):1219-25. PubMed ID: 1401059
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and biochemical spectrum of D-bifunctional protein deficiency.
    Ferdinandusse S; Denis S; Mooyer PA; Dekker C; Duran M; Soorani-Lunsing RJ; Boltshauser E; Macaya A; Gärtner J; Majoie CB; Barth PG; Wanders RJ; Poll-The BT
    Ann Neurol; 2006 Jan; 59(1):92-104. PubMed ID: 16278854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Morphological investigation of two sibling autopsy cases of mitochondrial trifunctional protein deficiency.
    Emura I; Usuda H
    Pathol Int; 2003 Nov; 53(11):775-9. PubMed ID: 14629302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria.
    Venizelos N; Ijlst L; Wanders RJ; Hagenfeldt L
    Pediatr Res; 1994 Jul; 36(1 Pt 1):111-4. PubMed ID: 7936829
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.
    Ibdah JA; Bennett MJ; Rinaldo P; Zhao Y; Gibson B; Sims HF; Strauss AW
    N Engl J Med; 1999 Jun; 340(22):1723-31. PubMed ID: 10352164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
    Miyajima H; Orii KE; Shindo Y; Hashimoto T; Shinka T; Kuhara T; Matsumoto I; Shimizu H; Kaneko E
    Neurology; 1997 Sep; 49(3):833-7. PubMed ID: 9305349
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit.
    Weinberger MJ; Rinaldo P; Strauss AW; Bennett MJ
    Biochem Biophys Res Commun; 1995 Apr; 209(1):47-52. PubMed ID: 7726862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein.
    van Grunsven EG; van Roermund CW; Denis S; Wanders RJ
    Biochem Biophys Res Commun; 1997 Jun; 235(1):176-9. PubMed ID: 9196058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies.
    Lundy CT; Shield JP; Kvittingen EA; Vinorum OJ; Trimble ER; Morris AA
    J Inherit Metab Dis; 2003; 26(6):537-41. PubMed ID: 14605499
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial trifunctional protein deficiency with recurrent rhabdomyolysis.
    Scheuerman O; Wanders RJ; Waterham HR; Dubnov-Raz G; Garty BZ
    Pediatr Neurol; 2009 Jun; 40(6):465-7. PubMed ID: 19433283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Trifunctional protein deficiency and long-chain-3-hydroxy-acyl CoA dehydrogenase deficiency].
    Kimura M; Yamaguchi S
    Ryoikibetsu Shokogun Shirizu; 2001; (36):77-9. PubMed ID: 11596456
    [No Abstract]   [Full Text] [Related]  

  • 20. Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.
    Liewluck T; Mundi MS; Mauermann ML
    Muscle Nerve; 2013 Dec; 48(6):989-91. PubMed ID: 23868323
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.