The components of adult astigmatism and their age-related changes

Autor: Hershko S, Lorenz K, von Trentini M, Pomares E, Corral M, Bataille L, Alio J, Rozema J, Jongenelen S, Ruiz-Hidalgo I, Tassignon M, Rauscher F, Blusch M, Dawczynski J, Wiedemann P, Mosca L, Guccione L, Riso M, Toro M, Rosati A, Duch F, Escude R, Martinez A, Morilla-Grasa A, Peris-Martinez C, Ajenjo A, Domene C, De Febrer M, Solans T, Gazdik A, Varssano D, Gold B, Toto L, Mastropasqua A, Mastropasqua L, Fasce F, Spinelli A, Knutsson K, Fogliato G, EVICR net Project Gullstrand Study

Publikováno v: OPHTHALMIC AND PHYSIOLOGICAL OPTICS
r-FISABIO. Repositorio Institucional de Producción Científica
instname

Purpose To study the corneal and internal astigmatism and the age-related changes underlying the known refractive shift with-the-rule (WTR) towards against-the-rule (ATR) astigmatism. Methods Refractive and corneal biometry data were collected for a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::fdbf89d3c88082a24c11fc58e730c575
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=11550

Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online

Autor: Mg, Miano, Valverde D, Solans T, Grammatico B, Migliaccio C, Cirigliano V, DeBernardo C, Ventruto V, Thomas Meitinger, Wright A, Del Porto G, Baiget M, D'Urso M, Ciccodicola A

Publikováno v: Scopus-Elsevier
Europe PubMed Central
Human mutation (Online) 12 (1998): 212–213.
info:cnr-pdr/source/autori:Miano MG, Valverde D, Solans T, Grammatico B, Migliaccio C, Cirigliano V, DeBernardo C, Ventruto V, Meitinger T, Wright A, Del Porto G, Baiget M, D'Urso M, Ciccodicola A./titolo:Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online./doi:/rivista:Human mutation (Online)/anno:1998/pagina_da:212/pagina_a:213/intervallo_pagine:212–213/volume:12

Recently a new gene called RPGR (retinitis pigmentosa GTPase regulator) was isolated in Xp21.1 and found to be mutated in patients with RP3 type X-linked retinitis pigmentosa. Two new mutations, the first a single base pair deletion and the other a t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::738f699b2698d11beeb45ee32d738bca
https://pubmed.ncbi.nlm.nih.gov/10651485

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

Autor: Bayés, M, Goldaracena, B, Martínez-Mir, A, Iragui-Madoz, M I, Solans, T, Chivelet, P, Bussaglia, E, Ramos-Arroyo, M A, Baiget, M, Vilageliu, L, Balcells, S, Gonzàlez-Duarte, R, Grinberg, D

Publikováno v: Journal of Medical Genetics; Feb1998, Vol. 35 Issue 2, p141-145, 5p, 1 Color Photograph, 1 Diagram, 2 Charts