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 *

152 related articles for article (PubMed ID: 15733276)

  • 21. Retinopathy of prematurity: mutations in the Norrie disease gene and the risk of progression to advanced stages.
    Haider MZ; Devarajan LV; Al-Essa M; Srivastva BS; Kumar H; Azad R; Rashwan N
    Pediatr Int; 2001 Apr; 43(2):120-3. PubMed ID: 11285060
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Familial exudative Criswick-Schepens vitreoretinopathy].
    Chynoranský M; Gerinec A; Streicher T
    Cesk Oftalmol; 1989 Sep; 45(5):334-40. PubMed ID: 2805106
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Asymmetric familial exudative vitreoretinopathy in a premature infant misdiagnosed as retinopathy of prematurity.
    Yang Y; Zhang W
    Clin Exp Optom; 2024 May; 107(4):469-472. PubMed ID: 36948182
    [No Abstract]   [Full Text] [Related]  

  • 24. Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.
    Shastry BS; Pendergast SD; Hartzer MK; Liu X; Trese MT
    Arch Ophthalmol; 1997 May; 115(5):651-5. PubMed ID: 9152134
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.
    Robitaille JM; Zheng B; Wallace K; Beis MJ; Tatlidil C; Yang J; Sheidow TG; Siebert L; Levin AV; Lam WC; Arthur BW; Lyons CJ; Jaakkola E; Tsilou E; Williams CA; Weaver RG; Shields CL; Guernsey DL
    Br J Ophthalmol; 2011 Apr; 95(4):574-9. PubMed ID: 21097938
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees.
    Robitaille JM; Wallace K; Zheng B; Beis MJ; Samuels M; Hoskin-Mott A; Guernsey DL
    Ophthalmic Genet; 2009 Mar; 30(1):23-30. PubMed ID: 19172507
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Ocular changes in premature infants with a birth weight of 1000 g or less (with special reference to retinopathia prematurorum)].
    Pelle Z
    Orv Hetil; 1988 Aug; 129(32):1695-8. PubMed ID: 3050747
    [No Abstract]   [Full Text] [Related]  

  • 28. Published genetic variants in retinopathy of prematurity: random forest analysis suggests a negligible contribution to risk and severity.
    Dunai G; Vásárhelyi B; Szabó M; Hajdú J; Mészáros G; Tulassay T; Treszl A
    Curr Eye Res; 2008 May; 33(5):501-5. PubMed ID: 18568888
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [No disorder of arachidonic acid-induced thrombocyte aggregation in familial exudative vitreoretinopathy].
    Bopp S; Wagner T; Laqua H
    Klin Monbl Augenheilkd; 1989 Jan; 194(1):13-5. PubMed ID: 2496260
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two cases of dominant exudative vitreoretinopathy.
    Van Herck M; Leys A; Missotten L
    Bull Soc Belge Ophtalmol; 1982; 203():93-7. PubMed ID: 7187626
    [No Abstract]   [Full Text] [Related]  

  • 31. Familial exudative vitreoretinopathy in a premature child.
    Gologorsky D; Chang JS; Hess DJ; Berrocal AM
    Ophthalmic Surg Lasers Imaging Retina; 2013 Nov; 44(6):603-5. PubMed ID: 24144178
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
    Toomes C; Bottomley HM; Jackson RM; Towns KV; Scott S; Mackey DA; Craig JE; Jiang L; Yang Z; Trembath R; Woodruff G; Gregory-Evans CY; Gregory-Evans K; Parker MJ; Black GC; Downey LM; Zhang K; Inglehearn CF
    Am J Hum Genet; 2004 Apr; 74(4):721-30. PubMed ID: 15024691
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Screening analysis of retinopathy of prematurity and treatment of threshold retinopathy of prematurity].
    Huang ZN; Yin DM; Huang DR; Liang SX
    Zhonghua Yan Ke Za Zhi; 2006 Jun; 42(6):496-500. PubMed ID: 16857127
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Diagnostic and Therapeutic Challenges.
    Thomas M; Shah AR; Besirli CG; Drenser KA
    Retina; 2019 Apr; 39(4):794-797. PubMed ID: 29360685
    [No Abstract]   [Full Text] [Related]  

  • 35. Familial exudative vitreoretinopathy: multiple modes of inheritance.
    Shastry BS; Hartzer MK; Trese MT
    Clin Genet; 1993 Nov; 44(5):275-6. PubMed ID: 8313628
    [No Abstract]   [Full Text] [Related]  

  • 36. Genetic evaluation to establish the diagnosis of X-linked familial exudative vitreoretinopathy.
    Drenser KA; Dailey W; Capone A; Trese MT
    Ophthalmic Genet; 2006 Sep; 27(3):75-8. PubMed ID: 17050281
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Similarity of familial exudative vitreoretinopathy and retinopathy of prematurity.
    Campo RV
    Arch Ophthalmol; 1983 May; 101(5):821. PubMed ID: 6687800
    [No Abstract]   [Full Text] [Related]  

  • 38. [Persistence and hyperplasia of the primary vitreous body].
    Gonvers M; Faggioni R; Zografos L; Gailloud C
    Adv Ophthalmol; 1977; 34():74-92. PubMed ID: 577376
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Vaginal delivery and threshold retinopathy of prematurity.
    Uparkar M; Uparkar U; Natarajan S
    Acta Paediatr; 2007 Oct; 96(10):1552. PubMed ID: 17714545
    [No Abstract]   [Full Text] [Related]  

  • 40. Screening for retinopathy of prematurity: results of a 7-year study of underweight newborns.
    Flores-Santos R; Hernández-Cabrera MA; Henández-Herrera RJ; Sepúlveda-Cañamar F
    Arch Med Res; 2007 May; 38(4):440-3. PubMed ID: 17416292
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.