172 related articles for article (PubMed ID: 15761389)
41. Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark.
Hove MN; Kilic-Biyik KZ; Trotter A; Grønskov K; Sander B; Larsen M; Carroll J; Bech-Hansen T; Rosenberg T
Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6861-6869. PubMed ID: 28002560
[TBL] [Abstract][Full Text] [Related]
42. A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness.
Jacobi FK; Hamel CP; Arnaud B; Blin N; Broghammer M; Jacobi PC; Apfelstedt-Sylla E; Pusch CM
Am J Ophthalmol; 2003 May; 135(5):733-6. PubMed ID: 12719097
[TBL] [Abstract][Full Text] [Related]
43. Cacna1f gene decreased contractility of skeletal muscle in rat model with congenital stationary night blindness.
An J; Zhang L; Jiao B; Lu F; Xia F; Yu Z; Zhang Z
Gene; 2015 May; 562(2):210-9. PubMed ID: 25748727
[TBL] [Abstract][Full Text] [Related]
44. The Ca(v)1.4 calcium channel: more than meets the eye.
Doering CJ; Peloquin JB; McRory JE
Channels (Austin); 2007; 1(1):3-10. PubMed ID: 19151588
[TBL] [Abstract][Full Text] [Related]
45. Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.
Malaichamy S; Sen P; Sachidanandam R; Arokiasamy T; Lancelot ME; Audo I; Zeitz C; Soumittra N
Mol Vis; 2014; 20():341-51. PubMed ID: 24715752
[TBL] [Abstract][Full Text] [Related]
46. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
Ruether K; Apfelstedt-Sylla E; Zrenner E
Ger J Ophthalmol; 1993 Nov; 2(6):429-35. PubMed ID: 8312830
[TBL] [Abstract][Full Text] [Related]
47. CSNB1 in Chinese families associated with novel mutations in NYX.
Xiao X; Jia X; Guo X; Li S; Yang Z; Zhang Q
J Hum Genet; 2006; 51(7):634-40. PubMed ID: 16670814
[TBL] [Abstract][Full Text] [Related]
48. Novel frameshift mutation in
Ivanova ME; Zolnikova IV; Gorgisheli KV; Atarshchikov DS; Ghosh P; Barh D
Ophthalmic Genet; 2019 Dec; 40(6):558-563. PubMed ID: 31826698
[No Abstract] [Full Text] [Related]
49. The importance of genetic testing as demonstrated by two cases of
Men CJ; Bujakowska KM; Comander J; Place E; Bedoukian EC; Zhu X; Leroy BP; Fulton AB; Pierce EA
Mol Vis; 2017; 23():695-706. PubMed ID: 29062221
[TBL] [Abstract][Full Text] [Related]
50. Congenital Stationary Night Blindness: Clinical and Genetic Features.
Kim AH; Liu PK; Chang YH; Kang EY; Wang HH; Chen N; Tseng YJ; Seo GH; Lee H; Liu L; Chao AN; Chen KJ; Hwang YS; Wu WC; Lai CC; Tsang SH; Hsiao MC; Wang NK
Int J Mol Sci; 2022 Nov; 23(23):. PubMed ID: 36499293
[TBL] [Abstract][Full Text] [Related]
51.
Scanga HL; Liasis A; Pihlblad MS; Nischal KK
Ophthalmic Genet; 2021 Oct; 42(5):588-592. PubMed ID: 34165036
[No Abstract] [Full Text] [Related]
52. Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness.
Schuster A; Pusch CM; Gamer D; Apfelstedt-Sylla E; Zrenner E; Kurtenbach A
Int J Mol Med; 2005 Jan; 15(1):159-67. PubMed ID: 15583843
[TBL] [Abstract][Full Text] [Related]
53. CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosis.
Yzer S; Fishman GA; Racine J; Al-Zuhaibi S; Chakor H; Dorfman A; Szlyk J; Lachapelle P; van den Born LI; Allikmets R; Lopez I; Cremers FP; Koenekoop RK
Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3736-44. PubMed ID: 16936081
[TBL] [Abstract][Full Text] [Related]
54. Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
Mansergh F; Orton NC; Vessey JP; Lalonde MR; Stell WK; Tremblay F; Barnes S; Rancourt DE; Bech-Hansen NT
Hum Mol Genet; 2005 Oct; 14(20):3035-46. PubMed ID: 16155113
[TBL] [Abstract][Full Text] [Related]
55. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
Boycott KM; Pearce WG; Bech-Hansen NT
Can J Ophthalmol; 2000 Jun; 35(4):204-13. PubMed ID: 10900517
[TBL] [Abstract][Full Text] [Related]
56. Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
Lodha N; Bonfield S; Orton NC; Doering CJ; McRory JE; Mema SC; Rehak R; Sauvé Y; Tobias R; Stell WK; Bech-Hansen NT
Adv Exp Med Biol; 2010; 664():549-58. PubMed ID: 20238058
[TBL] [Abstract][Full Text] [Related]
57. X-linked cone dysfunction syndrome with myopia and protanopia.
Michaelides M; Johnson S; Bradshaw K; Holder GE; Simunovic MP; Mollon JD; Moore AT; Hunt DM
Ophthalmology; 2005 Aug; 112(8):1448-54. PubMed ID: 15953640
[TBL] [Abstract][Full Text] [Related]
58. Possible pathogenesis of congenital stationary night blindness.
Kato M; Aonuma H; Kawamura H; Miura Y; Watanabe I
Jpn J Ophthalmol; 1987; 31(1):88-101. PubMed ID: 3498070
[TBL] [Abstract][Full Text] [Related]
59. Nightblindness-associated transient tonic downgaze (NATTD) in infant boys with chin-up head posture.
Simonsz HJ; Florijn RJ; van Minderhout HM; Bergen AA; Kamermans M
Strabismus; 2009; 17(4):158-64. PubMed ID: 20001510
[TBL] [Abstract][Full Text] [Related]
60. A comparison of ERG abnormalities in XLRS and XLCSNB.
Bradshaw K; Allen L; Trump D; Hardcastle A; George N; Moore A
Doc Ophthalmol; 2004 Mar; 108(2):135-45. PubMed ID: 15455796
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
