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 *

179 related articles for article (PubMed ID: 8094173)

  • 21. 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]  

  • 22. Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.
    Matern D; Schehata BM; Shekhawa P; Strauss AW; Bennett MJ; Rinaldo P
    Mol Genet Metab; 2001 Mar; 72(3):265-8. PubMed ID: 11243734
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD deficiency.
    Jones PM; Butt Y; Bennett MJ
    Pediatr Res; 2003 May; 53(5):783-7. PubMed ID: 12621125
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [EBV infection revealing a long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency in a 3-year-old boy].
    Desbrée A; Houdon L; Touati G; Djemili S; Choker G; Flodrops H
    Arch Pediatr; 2011 Jan; 18(1):18-22. PubMed ID: 21035315
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Pregnancy and inborn errors of metabolism].
    Radomyska B
    Ginekol Pol; 2003 Jun; 74(6):479-85. PubMed ID: 12931456
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Acute fatty liver in pregnancy: revealing fetal fatty acid oxidation disorders].
    Lamireau D; Feghali H; Redonnet-Vernhet I; Mesli S; Carles D; Brissaud O
    Arch Pediatr; 2012 Mar; 19(3):277-81. PubMed ID: 22325456
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Variation of long-chain 3-hydroxyacyl-CoA dehydrogenase DNA methylation in placenta of different preeclampsia-like mouse models].
    Han Y; Yang Z; Ding X; Yu H; Yi Y
    Zhonghua Fu Chan Ke Za Zhi; 2015 Oct; 50(10):740-6. PubMed ID: 26675572
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.
    den Boer ME; Wanders RJ; Morris AA; IJlst L; Heymans HS; Wijburg FA
    Pediatrics; 2002 Jan; 109(1):99-104. PubMed ID: 11773547
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Paternal isodisomy of chromosome 2 as a cause of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.
    Baskin B; Geraghty M; Ray PN
    Am J Med Genet A; 2010 Jul; 152A(7):1808-11. PubMed ID: 20583174
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.
    Chakrapani A; Olpin S; Cleary M; Walter JH; Wraith JE; Besley GT
    J Inherit Metab Dis; 2000 Dec; 23(8):826-34. PubMed ID: 11196108
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations.
    Yang Z; Zhao Y; Bennett MJ; Strauss AW; Ibdah JA
    Am J Obstet Gynecol; 2002 Sep; 187(3):715-20. PubMed ID: 12237653
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency.
    von Döbeln U; Venizelos N; Westgren M; Hagenfeldt L
    J Inherit Metab Dis; 1994; 17(2):185-8. PubMed ID: 7967472
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evidence for fatty acid oxidation in human placenta, and the relationship of fatty acid oxidation enzyme activities with gestational age.
    Rakheja D; Bennett MJ; Foster BM; Domiati-Saad R; Rogers BB
    Placenta; 2002 May; 23(5):447-50. PubMed ID: 12061861
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).
    Otto LR; Boriack RL; Marsh DJ; Kum JB; Eng C; Burlina AB; Bennett MJ
    Am J Med Genet; 1999 Mar; 83(1):3-5. PubMed ID: 10076877
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency and choroidal neovascularization].
    Stopek D; Gitteau Lala E; Labarthe F; Le Lez ML; Majzoub S; Castelnau P; Pisella PJ
    J Fr Ophtalmol; 2008 Dec; 31(10):993-8. PubMed ID: 19107076
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The long-chain 3-hydroxyacyl-CoA dehydrogenase of human liver mitochondria.
    Carpenter K; Middleton B; Pollitt RJ
    J Inherit Metab Dis; 1991; 14(3):321-4. PubMed ID: 1770783
    [No Abstract]   [Full Text] [Related]  

  • 38. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Tyni T; Pihko H
    Acta Paediatr; 1999 Mar; 88(3):237-45. PubMed ID: 10229030
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Lawlor DP; Kalina RE
    Am J Ophthalmol; 1997 Jun; 123(6):846-8. PubMed ID: 9535636
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency.
    Gillingham MB; Weleber RG; Neuringer M; Connor WE; Mills M; van Calcar S; Ver Hoeve J; Wolff J; Harding CO
    Mol Genet Metab; 2005; 86(1-2):124-33. PubMed ID: 16040264
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.