BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

878 related articles for article (PubMed ID: 9593380)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Ophthalmologic abnormalities in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: presentation of a long-term survivor.
    Sturm V
    Eur J Ophthalmol; 2008; 18(3):476-8. PubMed ID: 18465739
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-term pattern of progression of myopic maculopathy: a natural history study.
    Hayashi K; Ohno-Matsui K; Shimada N; Moriyama M; Kojima A; Hayashi W; Yasuzumi K; Nagaoka N; Saka N; Yoshida T; Tokoro T; Mochizuki M
    Ophthalmology; 2010 Aug; 117(8):1595-611, 1611.e1-4. PubMed ID: 20207005
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Long-term follow-up of Stargardt's disease and fundus flavimaculatus.
    Armstrong JD; Meyer D; Xu S; Elfervig JL
    Ophthalmology; 1998 Mar; 105(3):448-57; discussion 457-8. PubMed ID: 9499775
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multifocal chorioretinal lesions in Borzoi dogs.
    Storey ES; Grahn BH; Alcorn J
    Vet Ophthalmol; 2005; 8(5):337-47. PubMed ID: 16178845
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical features and linkage analysis for a Chinese family with autosomal dominant central areolar choroidal dystrophy.
    Ma K; Yang XF; Han C; Zhang N; Xu J; Liu SB; Lu H; Snellingen T; Wang NL; Liu NP
    Chin Med J (Engl); 2009 Nov; 122(22):2686-90. PubMed ID: 19951596
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.
    Renner AB; Kellner U; Cropp E; Preising MN; MacDonald IM; van den Hurk JA; Cremers FP; Foerster MH
    Ophthalmology; 2006 Nov; 113(11):2066.e1-10. PubMed ID: 16935340
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and image-guided chorioretinal findings in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Turaka K; Bryan JS; Gordon AJ; Kwong HM; Reddy R; Tsipursky M; Sell CH
    J Pediatr Endocrinol Metab; 2012; 25(5-6):565-7. PubMed ID: 22876558
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late onset is common in best macular dystrophy associated with VMD2 gene mutations.
    Renner AB; Tillack H; Kraus H; Krämer F; Mohr N; Weber BH; Foerster MH; Kellner U
    Ophthalmology; 2005 Apr; 112(4):586-92. PubMed ID: 15808248
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fundus autofluorescence imaging in Best's vitelliform dystrophy.
    Jarc-Vidmar M; Kraut A; Hawlina M
    Klin Monbl Augenheilkd; 2003 Dec; 220(12):861-7. PubMed ID: 14704944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Refined staging for chorioretinopathy in long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency.
    Tyni T; Immonen T; Lindahl P; Majander A; Kivelä T
    Ophthalmic Res; 2012; 48(2):75-81. PubMed ID: 22473002
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.
    Rotenstreich Y; Fishman GA; Anderson RJ
    Ophthalmology; 2003 Jun; 110(6):1151-8. PubMed ID: 12799240
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Longitudinal cohort study of patients with birdshot chorioretinopathy. IV. Visual field results at baseline.
    Gordon LK; Monnet D; Holland GN; Brézin AP; Yu F; Levinson RD
    Am J Ophthalmol; 2007 Dec; 144(6):829-837. PubMed ID: 17937923
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical findings in a carrier of a new mutation in the choroideremia gene.
    Potter MJ; Wong E; Szabo SM; McTaggart KE
    Ophthalmology; 2004 Oct; 111(10):1905-9. PubMed ID: 15465555
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-term results of submacular surgery combined with macular translocation of the retinal pigment epithelium in neovascular age-related macular degeneration.
    MacLaren RE; Bird AC; Sathia PJ; Aylward GW
    Ophthalmology; 2005 Dec; 112(12):2081-7. PubMed ID: 16325706
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuro-ophthalmic presentation of cone dysfunction syndromes in the adult.
    Zervas JP; Smith JL
    J Clin Neuroophthalmol; 1987 Dec; 7(4):202-18. PubMed ID: 2963026
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 44.