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 *

141 related articles for article (PubMed ID: 19107076)

  • 1. [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]  

  • 2. 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]  

  • 3. Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Tyni T; Paetau A; Strauss AW; Middleton B; Kivelä T
    Pediatr Res; 2004 Nov; 56(5):744-50. PubMed ID: 15347768
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T; Kivelä T; Lappi M; Summanen P; Nikoskelainen E; Pihko H
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency and progressive retinopathy: one case report followed by ERGs, VEPs, EOG over a 17-year period.
    Rigaudière F; Delouvrier E; Le Gargasson JF; Milani P; Ogier de Baulny H; Schiff M
    Doc Ophthalmol; 2021 Jun; 142(3):371-380. PubMed ID: 33392894
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.
    Sims HF; Brackett JC; Powell CK; Treem WR; Hale DE; Bennett MJ; Gibson B; Shapiro S; Strauss AW
    Proc Natl Acad Sci U S A; 1995 Jan; 92(3):841-5. PubMed ID: 7846063
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Long-chain fatty acid oxidation during early human development.
    Oey NA; den Boer ME; Wijburg FA; Vekemans M; Augé J; Steiner C; Wanders RJ; Waterham HR; Ruiter JP; Attié-Bitach T
    Pediatr Res; 2005 Jun; 57(6):755-9. PubMed ID: 15845636
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?
    Holub M; Bodamer OA; Item C; Mühl A; Pollak A; Stöckler-Ipsiroglu S
    Acta Paediatr; 2005 Jan; 94(1):48-52. PubMed ID: 15858960
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication?
    Eskelin PM; Laitinen KA; Tyni TA
    Mol Genet Metab; 2010 Jun; 100(2):204-6. PubMed ID: 20363656
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ophthalmic pathology in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation.
    Tyni T; Pihko H; Kivelä T
    Curr Eye Res; 1998 Jun; 17(6):551-9. PubMed ID: 9663844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ocular characteristics in 10 children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a cross-sectional study with long-term follow-up.
    Fahnehjelm KT; Holmström G; Ying L; Haglind CB; Nordenström A; Halldin M; Alm J; Nemeth A; von Döbeln U
    Acta Ophthalmol; 2008 May; 86(3):329-37. PubMed ID: 18162058
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [LCHAD (long-chain 3-hydroxyacyl-CoA dehydrogenase) deficiency as a cause of sudden death of a three months old infant].
    Neuman-Łaniec M; Wierzba J; Irga N; Zaborowska-Sołtys M; Balcerska A
    Med Wieku Rozwoj; 2002; 6(3):221-6. PubMed ID: 12637776
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings].
    Deltetto N; Maxit C; Marchione D; Szlago M; Schenone A; Besada CH; Vaccarezza M; Agosta G
    Arch Argent Pediatr; 2012 Aug; 110(4):e63-6. PubMed ID: 22859334
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Jackson S; Bartlett K; Land J; Moxon ER; Pollitt RJ; Leonard JV; Turnbull DM
    Pediatr Res; 1991 Apr; 29(4 Pt 1):406-11. PubMed ID: 1830138
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia.
    Ibdah JA; Dasouki MJ; Strauss AW
    J Inherit Metab Dis; 1999 Oct; 22(7):811-4. PubMed ID: 10518281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency.
    Wilcken B; Leung KC; Hammond J; Kamath R; Leonard JV
    Lancet; 1993 Feb; 341(8842):407-8. PubMed ID: 8094173
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.