166 related articles for article (PubMed ID: 27157923)
41. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.
Souied E; Amalric P; Chauvet ML; Chevallier C; Le Hoang P; Munnich A; Kaplan J
Ophthalmic Genet; 1995 Mar; 16(1):11-5. PubMed ID: 7648037
[TBL] [Abstract][Full Text] [Related]
42. Hypotrichosis with juvenile macular dystrophy: Portuguese case.
Elfatoiki FZ; Cordoliani F; Pascal Regane P; Afforitit-Demoge A
Dermatol Online J; 2016 May; 22(5):. PubMed ID: 27617529
[TBL] [Abstract][Full Text] [Related]
43. Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations.
Bonilha VL; Rayborn ME; Bell BA; Marino MJ; Fishman GA; Hollyfield JG
Ophthalmic Genet; 2016 Jun; 37(2):150-60. PubMed ID: 25265374
[TBL] [Abstract][Full Text] [Related]
44. Macular function and morphologic features in juvenile stargardt disease: longitudinal study.
Testa F; Melillo P; Di Iorio V; Orrico A; Attanasio M; Rossi S; Simonelli F
Ophthalmology; 2014 Dec; 121(12):2399-405. PubMed ID: 25097154
[TBL] [Abstract][Full Text] [Related]
45. Dual AAV Vectors for Stargardt Disease.
Trapani I
Methods Mol Biol; 2018; 1715():153-175. PubMed ID: 29188512
[TBL] [Abstract][Full Text] [Related]
46. Effective delivery of large genes to the retina by dual AAV vectors.
Trapani I; Colella P; Sommella A; Iodice C; Cesi G; de Simone S; Marrocco E; Rossi S; Giunti M; Palfi A; Farrar GJ; Polishchuk R; Auricchio A
EMBO Mol Med; 2014 Feb; 6(2):194-211. PubMed ID: 24150896
[TBL] [Abstract][Full Text] [Related]
47. Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.
Chen Y; Ratnam K; Sundquist SM; Lujan B; Ayyagari R; Gudiseva VH; Roorda A; Duncan JL
Invest Ophthalmol Vis Sci; 2011 May; 52(6):3281-92. PubMed ID: 21296825
[TBL] [Abstract][Full Text] [Related]
48. Progression of Late-Onset Stargardt Disease.
Lambertus S; Lindner M; Bax NM; Mauschitz MM; Nadal J; Schmid M; Schmitz-Valckenberg S; den Hollander AI; Weber BH; Holz FG; van der Wilt GJ; Fleckenstein M; Hoyng CB;
Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5186-5191. PubMed ID: 27699414
[TBL] [Abstract][Full Text] [Related]
49. Dual
Dyka FM; Molday LL; Chiodo VA; Molday RS; Hauswirth WW
Hum Gene Ther; 2019 Nov; 30(11):1361-1370. PubMed ID: 31418294
[TBL] [Abstract][Full Text] [Related]
50. Retinal phenotypic characterization of patients with
López-Rubio S; Chacon-Camacho OF; Matsui R; Guadarrama-Vallejo D; Astiazarán MC; Zenteno JC
Mol Vis; 2018; 24():105-114. PubMed ID: 29422768
[TBL] [Abstract][Full Text] [Related]
51. Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration.
Mehat MS; Sundaram V; Ripamonti C; Robson AG; Smith AJ; Borooah S; Robinson M; Rosenthal AN; Innes W; Weleber RG; Lee RWJ; Crossland M; Rubin GS; Dhillon B; Steel DHW; Anglade E; Lanza RP; Ali RR; Michaelides M; Bainbridge JWB
Ophthalmology; 2018 Nov; 125(11):1765-1775. PubMed ID: 29884405
[TBL] [Abstract][Full Text] [Related]
52. Choroidal hyperreflective foci in Stargardt disease shown by spectral-domain optical coherence tomography imaging: correlation with disease severity.
Piri N; Nesmith BL; Schaal S
JAMA Ophthalmol; 2015 Apr; 133(4):398-405. PubMed ID: 25590640
[TBL] [Abstract][Full Text] [Related]
53. Full-field ERG as a predictor of the natural course of
Schroeder M; Kjellström U
Mol Vis; 2018; 24():1-16. PubMed ID: 29386879
[TBL] [Abstract][Full Text] [Related]
54. Disruption in Bruch membrane in patients with Stargardt disease.
Park SP; Chang S; Allikmets R; Smith RT; Burke TR; Gregory-Roberts E; Tsang SH
Ophthalmic Genet; 2012 Mar; 33(1):49-52. PubMed ID: 22060670
[TBL] [Abstract][Full Text] [Related]
55. P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle.
Shimomura Y; Wajid M; Shapiro L; Christiano AM
Development; 2008 Feb; 135(4):743-53. PubMed ID: 18199584
[TBL] [Abstract][Full Text] [Related]
56. Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease.
Lambertus S; Bax NM; Fakin A; Groenewoud JM; Klevering BJ; Moore AT; Michaelides M; Webster AR; van der Wilt GJ; Hoyng CB
PLoS One; 2017; 12(3):e0174020. PubMed ID: 28355279
[TBL] [Abstract][Full Text] [Related]
57. Identification of the PROM1 Mutation p.R373C in a Korean Patient With Autosomal Dominant Stargardt-like Macular Dystrophy.
Kim JM; Lee C; Lee GI; Kim NKD; Ki CS; Park WY; Kim BJ; Kim SJ
Ann Lab Med; 2017 Nov; 37(6):536-539. PubMed ID: 28840994
[TBL] [Abstract][Full Text] [Related]
58. Stargardt disease caused by a rare combination of double homozygous mutations.
Serapinas D; Obrikytė V; Sakalauskas R
Medicina (Kaunas); 2013; 49(8):386-91. PubMed ID: 24509150
[TBL] [Abstract][Full Text] [Related]
59. ELLIPSOID ZONE MAPPING AND OUTER RETINAL ASSESSMENT IN STARGARDT DISEASE.
Arepalli S; Traboulsi EI; Ehlers JP
Retina; 2018 Jul; 38(7):1427-1431. PubMed ID: 28613213
[TBL] [Abstract][Full Text] [Related]
60. P-cadherin regulates human hair growth and cycling via canonical Wnt signaling and transforming growth factor-β2.
Samuelov L; Sprecher E; Tsuruta D; Bíró T; Kloepper JE; Paus R
J Invest Dermatol; 2012 Oct; 132(10):2332-2341. PubMed ID: 22696062
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
