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 *

84 related articles for article (PubMed ID: 15489496)

  • 1. Norrie disease and peripheral venous insufficiency.
    Michaelides M; Luthert PJ; Cooling R; Firth H; Moore AT
    Br J Ophthalmol; 2004 Nov; 88(11):1475. PubMed ID: 15489496
    [No 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. Advanced bilateral persistent fetal vasculature associated with a novel mutation in the Norrie gene.
    Dhingra S; Shears DJ; Blake V; Stewart H; Patel CK
    Br J Ophthalmol; 2006 Oct; 90(10):1324-5. PubMed ID: 16980647
    [No Abstract]   [Full Text] [Related]  

  • 4. Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiency.
    Rehm HL; Gutiérrez-Espeleta GA; Garcia R; Jiménez G; Khetarpal U; Priest JM; Sims KB; Keats BJ; Morton CC
    Hum Mutat; 1997; 9(5):402-8. PubMed ID: 9143918
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epilepsy phenotypes in siblings with Norrie disease.
    Okumura A; Arai E; Kitamura Y; Abe S; Ikeno M; Fujimaki T; Yamamoto T; Shimizu T
    Brain Dev; 2015 Nov; 37(10):978-82. PubMed ID: 25944760
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy.
    Fuchs S; Kellner U; Wedemann H; Gal A
    Hum Mutat; 1995; 6(3):257-9. PubMed ID: 8535448
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Twenty years of audiology in a patient with Norrie disease.
    Halpin C; Sims K
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1705-10. PubMed ID: 18817988
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation of ophthalmic examination with carrier status in females potentially harboring a severe Norrie disease gene mutation.
    Khan AO; Aldahmesh MA; Meyer B
    Ophthalmology; 2008 Apr; 115(4):730-3. PubMed ID: 18387409
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
    Ramprasad VL; Thool A; Murugan S; Nancarrow D; Vyas P; Rao SK; Vidhya A; Ravishankar K; Kumaramanickavel G
    Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):17-23. PubMed ID: 15623749
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In utero diagnosis of Norrie disease and early laser preserves visual acuity.
    Kiernan DF; Blair MP; Shapiro MJ
    Arch Ophthalmol; 2010 Oct; 128(10):1382. PubMed ID: 20938020
    [No Abstract]   [Full Text] [Related]  

  • 12. Utilization of gene mapping and candidate gene mutation screening for diagnosing clinically equivocal conditions: a Norrie disease case study.
    Chini V; Stambouli D; Nedelea FM; Filipescu GA; Mina D; Kambouris M; El-Shantil H
    Eye Sci; 2014 Jun; 29(2):104-7. PubMed ID: 26011961
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24.
    Kim HJ; Hong SH; Ki CS; Kim BJ; Shim JS; Cho SH; Park JH; Kim JW
    Neurology; 2005 Jun; 64(11):1964-7. PubMed ID: 15955956
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplicate report crossing over in Norrie disease family.
    Ngo J; Spence MA; Cortessis V; Bateman JB; Sparkes RS
    Am J Med Genet; 1989 Jun; 33(2):286. PubMed ID: 2764042
    [No Abstract]   [Full Text] [Related]  

  • 15. [Mutational analysis in a family with X-linked spondyloepiphyseal dysplasia tarda].
    Zhu HY; Li J; Zhu RF; Wu X; Duan HL; Yang Y; Zhang Y; Hu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):421-3. PubMed ID: 18683141
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Wnt signaling pathway in familial exudative vitreoretinopathy and Norrie disease.
    Warden SM; Andreoli CM; Mukai S
    Semin Ophthalmol; 2007; 22(4):211-7. PubMed ID: 18097984
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dent's disease.
    Neild GH; Thakker RV; Unwin RJ; Wrong OM
    Nephrol Dial Transplant; 2005 Oct; 20(10):2284-5. PubMed ID: 16030051
    [No Abstract]   [Full Text] [Related]  

  • 18. [Norrie disease].
    Murano I
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):326-7. PubMed ID: 11528763
    [No Abstract]   [Full Text] [Related]  

  • 19. The involvement of genetic factors in chronic venous insufficiency.
    Hoţoleanui C; Jurj C
    Rom J Intern Med; 2008; 46(2):119-23. PubMed ID: 19284083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Infrequent X chromosome abnormality and X-linked syndromic deafness].
    Wang YJ; Shi XL; Nie JW; Ni B; Yin ZC; Dai HP
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2004 Oct; 29(5):500-3. PubMed ID: 16137031
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.