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 *

122 related articles for article (PubMed ID: 9228243)

  • 1. Histopathological and immunohistochemical findings associated with a null mutation in the Norrie disease gene.
    Schroeder B; Hesse L; Brück W; Gal A
    Ophthalmic Genet; 1997 Jun; 18(2):71-7. PubMed ID: 9228243
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis.
    Black GC; Perveen R; Bonshek R; Cahill M; Clayton-Smith J; Lloyd IC; McLeod D
    Hum Mol Genet; 1999 Oct; 8(11):2031-5. PubMed ID: 10484772
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and genetic analysis of Indian patients with NDP-related retinopathies.
    Sudha D; Ganapathy A; Mohan P; Mannan AU; Krishna S; Neriyanuri S; Swaminathan M; Rishi P; Chidambaram S; Arunachalam JP
    Int Ophthalmol; 2018 Jun; 38(3):1251-1260. PubMed ID: 28602015
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential diagnosis of Norrie disease and X-linked familial exudative vitreoretinopathy (XL-FEVR) based on clinical and molecular evaluation.
    Wawrocka A; Niedziela Z; Skorczyk-Werner A; Krawczynski MR
    Klin Oczna; 2016; 118(3):231-4. PubMed ID: 30088388
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel NDP mutation in an infant with unilateral persistent fetal vasculature and retinal vasculopathy.
    Aponte EP; Pulido JS; Ellison JW; Quiram PA; Mohney BG
    Ophthalmic Genet; 2009 Jun; 30(2):99-102. PubMed ID: 19373682
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
    Wu WC; Drenser K; Trese M; Capone A; Dailey W
    Arch Ophthalmol; 2007 Feb; 125(2):225-30. PubMed ID: 17296899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel frameshift c.22_25dupGCAT mutation of the NDP gene in a Chinese infant with Norrie disease: A case report.
    Wang H; Liu Z; Zhou Y; Ma Y; Tao D
    Medicine (Baltimore); 2022 Jan; 101(1):e28523. PubMed ID: 35029917
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cells.
    Lenzner S; Prietz S; Feil S; Nuber UA; Ropers HH; Berger W
    Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2825-33. PubMed ID: 12202498
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.
    Dickinson JL; Sale MM; Passmore A; FitzGerald LM; Wheatley CM; Burdon KP; Craig JE; Tengtrisorn S; Carden SM; Maclean H; Mackey DA
    Clin Exp Ophthalmol; 2006; 34(7):682-8. PubMed ID: 16970763
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Norrie disease in a family with a manifesting female carrier.
    Sims KB; Irvine AR; Good WV
    Arch Ophthalmol; 1997 Apr; 115(4):517-9. PubMed ID: 9109762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel c.287G>T
    Lin M; Lu Y; Sui Y; Ni X; Li H; Chen X; Zhao N; Jiang M
    Ophthalmic Genet; 2020 Aug; 41(4):338-340. PubMed ID: 32393149
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel missense NDP mutation [p.(Cys93Arg)] with a manifesting carrier in an austrian family with Norrie disease.
    Parzefall T; Lucas T; Ritter M; Ludwig M; Ramsebner R; Frohne A; Schöfer C; Hengstschläger M; Frei K
    Audiol Neurootol; 2014; 19(3):203-9. PubMed ID: 24801666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peripheral retinopathy in offspring of carriers of Norrie disease gene mutations. Possible transplacental effect of abnormal Norrin.
    Mintz-Hittner HA; Ferrell RE; Sims KB; Fernandez KM; Gemmell BS; Satriano DR; Caster J; Kretzer FL
    Ophthalmology; 1996 Dec; 103(12):2128-34. PubMed ID: 9003348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel missense Norrie disease mutation associated with a severe ocular phenotype.
    Khan AO; Shamsi FA; Al-Saif A; Kambouris M
    J Pediatr Ophthalmol Strabismus; 2004; 41(6):361-3. PubMed ID: 15609522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene.
    Payabvash S; Anderson JS; Nascene DR
    Neuroradiol J; 2015 Dec; 28(6):623-7. PubMed ID: 26459204
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal Diagnosis of a Case of Norrie Disease with Late Development of Bilateral Ocular Malformation.
    Wu LH; Chen LH; Xie H; Xie YJ
    Fetal Pediatr Pathol; 2017 Jun; 36(3):240-245. PubMed ID: 28394646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.
    Pelcastre EL; Villanueva-Mendoza C; Zenteno JC
    Clin Exp Ophthalmol; 2010 May; 38(4):367-74. PubMed ID: 20491809
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic heterogeneity associated with a novel mutation (Gly112Glu) in the Norrie disease protein.
    Allen RC; Russell SR; Streb LM; Alsheikheh A; Stone EM
    Eye (Lond); 2006 Feb; 20(2):234-41. PubMed ID: 15776010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy.
    Shastry BS
    Biochem Biophys Res Commun; 1998 May; 246(1):35-8. PubMed ID: 9618247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog.
    Joyce H; Burmeister LM; Wright H; Fleming L; Oliver JAC; Mellersh C
    PLoS One; 2021; 16(5):e0251071. PubMed ID: 33945575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.