BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 1789082)

  • 1. Autosomal dominant stationary night-blindness. A large family rediscovered.
    Rosenberg T; Haim M; Piczenik Y; Simonsen SE
    Acta Ophthalmol (Copenh); 1991 Dec; 69(6):694-702. PubMed ID: 1789082
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Family investigation and clinical genetic analysis of a large pedigree with congenital stationary night blindness].
    Fei YJ
    Zhonghua Yan Ke Za Zhi; 1992 May; 28(3):162-5. PubMed ID: 1286605
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A dominant form of congenital stationary night blindness (adCSNB) in a large Chinese family.
    Liu X; Zhuang S; Hu S; Zhang F; Lin B; Li X; Xu D; Chen SH
    Ann Hum Genet; 2005 May; 69(Pt 3):315-21. PubMed ID: 15845035
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.
    Gal A; Xu S; Piczenik Y; Eiberg H; Duvigneau C; Schwinger E; Rosenberg T
    Hum Mol Genet; 1994 Feb; 3(2):323-5. PubMed ID: 8004102
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Affected females in X-linked congenital stationary night blindness.
    Ruttum MS; Lewandowski MF; Bateman JB
    Ophthalmology; 1992 May; 99(5):747-52. PubMed ID: 1594221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG; Carr RE; Siegel IM
    Am J Ophthalmol; 1990 Jan; 109(1):44-8. PubMed ID: 2297031
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity.
    Hayakawa M; Imai Y; Wakita M; Kato K; Yanashima K; Miyake Y; Kanai A
    Ophthalmic Paediatr Genet; 1992 Dec; 13(4):211-7. PubMed ID: 1488221
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital stationary night blindness.
    Haim M
    Acta Ophthalmol (Copenh); 1986 Apr; 64(2):192-8. PubMed ID: 3487908
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Eisdell pedigree. Congenital stationary night-blindness with myopia.
    Jay M
    Trans Ophthalmol Soc U K (1962); 1983; 103 ( Pt 2)():221-6. PubMed ID: 6364465
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
    Bech-Hansen NT; Boycott KM; Gratton KJ; Ross DA; Field LL; Pearce WG
    Hum Genet; 1998 Aug; 103(2):124-30. PubMed ID: 9760193
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital stationary night blindness and a "Schubert-Bornschein" type electrophysiology in a family with dominant inheritance.
    Kabanarou SA; Holder GE; Fitzke FW; Bird AC; Webster AR
    Br J Ophthalmol; 2004 Aug; 88(8):1018-22. PubMed ID: 15258017
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rod and cone function in the Nougaret form of stationary night blindness.
    Sandberg MA; Pawlyk BS; Dan J; Arnaud B; Dryja TP; Berson EL
    Arch Ophthalmol; 1998 Jul; 116(7):867-72. PubMed ID: 9682699
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Congenital stationary night blindness].
    Svĕrák J; Jebavá R; Peregrin J; Zizka J; Hartmann M
    Cesk Slov Oftalmol; 1996 Jul; 52(3):135-42. PubMed ID: 8768469
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital stationary night blindness with negative electroretinogram. A new classification.
    Miyake Y; Yagasaki K; Horiguchi M; Kawase Y; Kanda T
    Arch Ophthalmol; 1986 Jul; 104(7):1013-20. PubMed ID: 3488053
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reduced amplitude of oscillatory potentials in female carriers of X-linked recessive congenital stationary night blindness.
    Miyake Y; Kawase Y
    Am J Ophthalmol; 1984 Aug; 98(2):208-15. PubMed ID: 6332537
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variable expressivity in X-linked congenital stationary night blindness.
    Pearce WG; Reedyk M; Coupland SG
    Can J Ophthalmol; 1990 Feb; 25(1):3-10. PubMed ID: 2328435
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
    Zeitz C; van Genderen M; Neidhardt J; Luhmann UF; Hoeben F; Forster U; Wycisk K; Mátyás G; Hoyng CB; Riemslag F; Meire F; Cremers FP; Berger W
    Invest Ophthalmol Vis Sci; 2005 Nov; 46(11):4328-35. PubMed ID: 16249515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked congenital stationary night blindness with myopia and nystagmus without clinical complaints of nyctalopia.
    Price MJ; Judisch GF; Thompson HS
    J Pediatr Ophthalmol Strabismus; 1988; 25(1):33-6. PubMed ID: 3257795
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Electrophysiologic tests for diagnosis of congenital night blindness].
    Lubiński W; Palacz A; Penkala K; Palacz O
    Klin Oczna; 1996 Jan; 98(1):9-12. PubMed ID: 9019583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
    al-Jandal N; Farrar GJ; Kiang AS; Humphries MM; Bannon N; Findlay JB; Humphries P; Kenna PF
    Hum Mutat; 1999; 13(1):75-81. PubMed ID: 9888392
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.