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 *

242 related articles for article (PubMed ID: 20491809)

  • 1. 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]  

  • 2. Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.
    Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez-Pardo A; Garcia-Hoyos M; Cantalapiedra D; Lorda-Sanchez I; Rodriguez de Alba M; Ramos C; Ayuso C
    Mol Vis; 2005 Sep; 11():705-12. PubMed ID: 16163268
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.
    Kondo H; Qin M; Kusaka S; Tahira T; Hasebe H; Hayashi H; Uchio E; Hayashi K
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1276-82. PubMed ID: 17325173
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.
    Chen ZY; Battinelli EM; Fielder A; Bundey S; Sims K; Breakefield XO; Craig IW
    Nat Genet; 1993 Oct; 5(2):180-3. PubMed ID: 8252044
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. A novel missense mutation of NDP in a Chinese family with X-linked familial exudative vitreoretinopathy.
    Liu HY; Huang J; Wang RL; Wang Y; Guo LJ; Li T; Wu D; Wang HD; Guo QN; Dong DQ
    J Chin Med Assoc; 2016 Nov; 79(11):633-638. PubMed ID: 27720678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening for NDP mutations in 44 unrelated patients with familial exudative vitreoretinopathy or Norrie disease.
    Yang H; Li S; Xiao X; Guo X; Zhang Q
    Curr Eye Res; 2012 Aug; 37(8):726-9. PubMed ID: 22563645
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR.
    Musada GR; Jalali S; Hussain A; Chururu AR; Gaddam PR; Chakrabarti S; Kaur I
    Mol Vis; 2016; 22():491-502. PubMed ID: 27217716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Novel Norrie disease gene mutations in Chinese patients with familial exudative vitreoretinopathy.
    Jia LY; Ma K
    BMC Ophthalmol; 2021 Feb; 21(1):84. PubMed ID: 33588793
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.
    Peng Y; Zhao R; Dai E; Peng L; He Y; Li S; Yang M
    Eur J Ophthalmol; 2022 Nov; 32(6):3220-3226. PubMed ID: 35037517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease.
    Liu J; Zhu J; Yang J; Zhang X; Zhang Q; Zhao P
    Mol Genet Genomic Med; 2019 Jan; 7(1):e00503. PubMed ID: 30474316
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. NDP-related retinopathies: clinical phenotype of female carriers.
    Huang L; Sun L; Li X; Li S; Zhang T; Zhang Z; Ding X
    Br J Ophthalmol; 2023 Aug; 107(8):1151-1155. PubMed ID: 35361573
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
    Rao FQ; Cai XB; Cheng FF; Cheng W; Fang XL; Li N; Huang XF; Li LH; Jin ZB
    Invest Ophthalmol Vis Sci; 2017 May; 58(5):2623-2629. PubMed ID: 28494495
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the proband.
    Lin P; Shankar SP; Duncan J; Slavotinek A; Stone EM; Rutar T
    J AAPOS; 2010 Feb; 14(1):93-6. PubMed ID: 20227630
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients.
    Yang M; Peng L; Lv L; Dai E; He Y; Zhao R; Li S
    Mol Genet Genomics; 2024 Mar; 299(1):32. PubMed ID: 38472449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.
    Zhang L; Yang Y; Li S; Tai Z; Huang L; Liu Y; Zhu X; Di Y; Qu C; Jiang Z; Li Y; Zhang G; Kim R; Sundaresan P; Yang Z; Zhu X
    Genet Test Mol Biomarkers; 2016 Jul; 20(7):346-51. PubMed ID: 27228167
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.