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 *

112 related articles for article (PubMed ID: 9895245)

  • 1. Isolated Norrie disease in a female caused by a balanced translocation t(X,6).
    Meire FM; Lafaut BA; Speleman F; Hanssens M
    Ophthalmic Genet; 1998 Dec; 19(4):203-7. PubMed ID: 9895245
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease gene.
    Kellner U; Fuchs S; Bornfeld N; Foerster MH; Gal A
    Ophthalmic Genet; 1996 Jun; 17(2):67-74. PubMed ID: 8832723
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unusual presentation of Norrie's disease with hypomagnesemia.
    Kumar MS; Shenoi A; Mukta Jain M; Ashok J; Chidananda SC; Sameera P; Maseeuddin S
    Indian Pediatr; 1998 Aug; 35(8):783-6. PubMed ID: 10216575
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [Keratotorus in Norrie disease].
    Lang GE; Rott HD; Naumann GO
    Klin Monbl Augenheilkd; 1991 Aug; 199(2):110-3. PubMed ID: 1960930
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Norrie syndrome: identification of carriers by segregation analysis with flanking DNA markers].
    Körner J; Uhlhaas S; Neugebauer M; Gal A
    Fortschr Ophthalmol; 1989; 86(1):78-81. PubMed ID: 2566566
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial exudative vitreoretinopathy mimicking persistent hyperplastic primary vitreous.
    Chang-Godinich A; Paysse EA; Coats DK; Holz ER
    Am J Ophthalmol; 1999 Apr; 127(4):469-71. PubMed ID: 10218708
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Norrie disease and exudative vitreoretinopathy in families with affected female carriers.
    Shastry BS; Hiraoka M; Trese DC; Trese MT
    Eur J Ophthalmol; 1999; 9(3):238-42. PubMed ID: 10544980
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A fetus with an X;1 balanced reciprocal translocation and eye disease.
    Seller MJ; Pal K; Horsley S; Davies AF; Berry AC; Meredith R; McCartney AC
    J Med Genet; 1995 Jul; 32(7):557-60. PubMed ID: 7562972
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Inversion (X)(p11.4q22) associated with Norrie disease in a four generation family.
    Pettenati MJ; Rao PN; Weaver RG; Thomas IT; McMahan MR
    Am J Med Genet; 1993 Mar; 45(5):577-80. PubMed ID: 8456827
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA.
    Vandeweyer G; Van der Aa N; Ceulemans B; van Bon BW; Rooms L; Kooy RF
    Epilepsy Res; 2012 May; 99(3):346-9. PubMed ID: 22245136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Intraocular cartilage in a microphthalmic eye of an otherwise healthy girl.
    Yanoff M; Font RL
    Arch Ophthalmol; 1969 Feb; 81(2):238-40. PubMed ID: 4974507
    [No Abstract]   [Full Text] [Related]  

  • 18. In-utero diagnosis of Norrie disease by ultrasonography.
    Redmond RM; Vaughan JI; Jay M; Jay B
    Ophthalmic Paediatr Genet; 1993 Mar; 14(1):1-3. PubMed ID: 8345950
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Repair of Total Tractional Retinal Detachment in Norrie Disease: Report of Technique and Successful Surgical Outcome.
    Todorich B; Thanos A; Yonekawa Y; Capone A
    Ophthalmic Surg Lasers Imaging Retina; 2017 Mar; 48(3):260-262. PubMed ID: 28297040
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.