Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Estefania Cobos"'
Autor:
Anna Esteve-Garcia, Estefania Cobos, Cristina Sau, Ariadna Padró-Miquel, Jaume Català-Mora, Pilar Barberán-Martínez, José M. Millán, Gema García-García, Cinthia Aguilera
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction:TULP1 exemplifies the remarkable clinical and genetic heterogeneity observed in inherited retinal dystrophies. Our research describes the clinical and molecular characteristics of a patient manifesting an atypical retinal dystrophy patte
Externí odkaz:
https://doaj.org/article/7498f0855a6149f8b650b1741e4a7da2
Autor:
Javier Obis, Luis Arias, Daniel Lorenzo, Noel Padron-Perez, Pere Garcia-Bru, Estefania Cobos, Rahul Morwani, Jose Caminal
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background The purpose of this study is to assess the effectiveness of topical nonsteroidal anti-inflammatory drugs (NSAIDs) and corticosteroids (intravitreal dexamethasone and peribulbar triamcinolone) in treating pseudophakic macular edema
Externí odkaz:
https://doaj.org/article/9b0b0f0784304ceb901c1272c5d82cb7
Autor:
Josep Maria Caminal, Daniel Lorenzo, Cristina Gutierrez, Andrea Slocker, Josep Maria Piulats, Estefania Cobos, Pere Garcia-Bru, Rahul Morwani, Juan Francisco Santamaria, Luis Arias
Publikováno v:
Journal of clinical medicine. 11(23)
Surgical resection is widely used to treat small tumours located in the iris and the ciliary body, due to the accessibility of these sites. By contrast, surgical removal of choroidal tumours is substantially more challenging, which is why this proced
Autor:
Jose Luis Manzano Mozo, Bibiana Quirant Sánchez, Aram Boada Garcia, Sandra Gomez Sanchez, Estefania Cobos Martin, Nina A. Richarz
Publikováno v:
Australasian Journal of Dermatology. 61:70-72
Autor:
Alba Gómez-Benlloch, Xavier Garrell-Salat, Estefanía Cobos, Elena López, Anna Esteve-Garcia, Sergi Ruiz, Meritxell Vázquez, Laura Sararols, Marc Biarnés
Publikováno v:
Diagnostics, Vol 14, Iss 9, p 878 (2024)
Macular dystrophies (MDs) constitute a collection of hereditary retina disorders leading to notable visual impairment, primarily due to progressive macular atrophy. These conditions are distinguished by bilateral and relatively symmetrical abnormalit
Externí odkaz:
https://doaj.org/article/06eb48e077c146d988cece4074becf24