OCTA and Microperimetry Changes Preceding the Appearance of Diabetic Retinopathy in Patients with Type 1 Diabetes.

Autor: Rego-Lorca D; Ophthalmology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain., Mateu-Salat M; Institut de Recerca Sant Pau (IR Sant Pau), Barcelona, Spain.; Endocrinology and Nutrition Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain., Chico A; Endocrinology and Nutrition Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; CIBER-BBN, Universitat Autònoma de Barcelona, Barcelona, Spain., Molina-Montero A; Optometry Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain., Díaz-Cascajosa J; Ophthalmology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Autonomous University of Barcelona, UAB, Barcelona, Spain., Vela-Segarra JI; Ophthalmology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Autonomous University of Barcelona, UAB, Barcelona, Spain.; Institut Comtal d'Oftalmologia (ICO), Barcelona, Spain.

Publikováno v: Current eye research [Curr Eye Res] 2024 Dec 05, pp. 1-5. Date of Electronic Publication: 2024 Dec 05.

Next generation sequencing uncovers a missense mutation in COL4A1 as the cause of familial retinal arteriolar tortuosity (vol 252, pg 1789, 2014)

Autor: Zenteno, JC, Crespi, J, Buentello-Volante, B, Buil, JA, Bassaganyas, F, Vela-Segarra, JI, Diaz-Cascajosa, J, Marieges, MT

Publikováno v: GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::1e213c8fb36d606ea1b5fc370093e7aa
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=8418

Erratum to: Next generation sequencing uncovers a missense mutation in COL4A1 as the cause of familial retinal arteriolar tortuosity.

Autor: Zenteno JC; Genetics Department and Research Unit, Institute of Ophthalmology 'Conde de Valenciana' and Biochemistry Department, Faculty of Medicine, National Autonomous University of Mexico (UNAM), Chimalpopoca 14, Col. Obrera, Mexico City, CP, 06800, Mexico, jczenteno@institutodeoftalmologia.org., Crespí J, Buentello-Volante B, Buil JA, Bassaganyas F, Vela-Segarra JI, Diaz-Cascajosa J, Marieges MT

Publikováno v: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie [Graefes Arch Clin Exp Ophthalmol] 2015 Aug; Vol. 253 (8), pp. 1417.

Pathogenic variants of MFRP and PRSS56 genes are major causes of nanophthalmos in Japanese patients.

Autor: Ota, Junya¹ (AUTHOR), Inooka, Taiga¹ (AUTHOR), Okado, Satoshi¹ (AUTHOR), Maeda, Natsuki² (AUTHOR), Koyanagi, Yoshito¹ (AUTHOR), Kominami, Taro¹ (AUTHOR), Nishiguchi, Koji M.¹ (AUTHOR), Ueno, Shinji^1,2 (AUTHOR) uenos@hirosaki-u.ac.jp

Publikováno v: Ophthalmic Genetics. Oct2023, Vol. 44 Issue 5, p423-429. 7p.

[Early treatment of idiopathic vasculitis, aneurysms and neuroretinitis (IRVAN). A case report].

Autor: Garcia Vilaro M; Servicio de Oftalmología, Hospital de la Santa Creu i Sant Pau, Barcelona, España. Electronic address: martagvilaro@hotmail.com., Bassaganyas Vilarrassa F; Servicio de Oftalmología, Hospital de la Santa Creu i Sant Pau, Barcelona, España., Vela Segarra JI; Servicio de Oftalmología, Hospital de la Santa Creu i Sant Pau, Barcelona, España., Buil Calvo JA; Servicio de Oftalmología, Hospital de la Santa Creu i Sant Pau, Barcelona, España.

Publikováno v: Archivos de la Sociedad Espanola de Oftalmologia [Arch Soc Esp Oftalmol] 2014 Mar; Vol. 89 (3), pp. 117-20. Date of Electronic Publication: 2012 Oct 23.