Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Sandrine, Boutboul"'
Publikováno v:
European journal of ophthalmology. 31(5)
Purpose: To describe the management and multimodal imaging of lattice corneal dystrophy type II (LCD-II) complicated by an infectious keratitis due to a bandage contact lens and to review current literature. Observation: A 50-year-old female was diag
Autor:
Olivier Touzeau, Vincent Borderie, Laurent Laroche, Cécile Allouch, Sandrine Boutboul, Pierre-Yves Boëlle
Publikováno v:
Ophthalmology. 116:2354-2360
Objective To analyze graft survival and the outcome of the corneal endothelium after corneal transplantation in a single model to predict the long-term prognosis of these grafts. Design Cohort study. Data were recorded prospectively and then analyzed
Autor:
Christine Chaumeil, Claudia Costa Ferreira, Laurent Laroche, L. Batellier, Sandrine Degorge, Sandrine Boutboul, Djida Benallaoua, Pablo Goldschmidt
Publikováno v:
British Journal of Ophthalmology. 93:258-262
Background:Propionibacteriaceae (Propioni) are anaerobic bacteria associated with human and animal infections. Present-day methods of diagnosis for Propioni are unsatisfactory due to a lack of sensitivity of culture, time required for culture results
Autor:
F Thomas, Sandrine Boutboul, Laurent Laroche, Vincent Borderie, Marie Baudrimont, Tristan Bourcier
Publikováno v:
Journal of Cataract and Refractive Surgery. 30:921-924
A 70-year-old man was referred to us with a 2-year, progressive, painless decrease in visual acuity in the right eye. Ocular history included extraction of a traumatic cataract with a transclerally fixated posterior chamber intraocular lens. Slitlamp
Publikováno v:
EMC - Ophtalmologie. 1:1-18
Publikováno v:
Acta Ophthalmologica. 90
Purpose A 38-year-old Egyptian man was referred to our department due to bilateral loss of vision over a six-year period.Slit lamp examination revealed extensive bilateral corneal opacitiesBlood analysis revealed lipid metabolism abnormalities with a
Autor:
Cécile Allouch, Elena Basli, Sandrine Degorge, L. Batellier, Sandrine Boutboul, Pablo Goldschmidt, Christine Chaumeil, Vincent Borderie, Djida Benallaoua, Laurent Laroche
Publikováno v:
British Journal of Ophthalmology
British Journal of Ophthalmology, BMJ Publishing Group, 2009, 93 (8), pp.1089-n/a. ⟨10.1136/bjo.2008.152181⟩
British Journal of Ophthalmology, BMJ Publishing Group, 2009, 93 (8), pp.1089-n/a. ⟨10.1136/bjo.2008.152181⟩
Diagnosis of bacterial endophthalmitis (BE) often fails due to: (1) insufficient volumes of vitreous fluid (VF) and aqueous humour (AH); (2) lack of sensitivity of culture; (3) antibiotic treatments; (4) polymerase chain reaction (PCR) cross-contamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe6a51593d4063f2723447193f21b49d
https://hal.archives-ouvertes.fr/hal-00477830/document
https://hal.archives-ouvertes.fr/hal-00477830/document
Autor:
Sandrine Boutboul, Vincent Borderie, Imène Letaief, M. Puech, Franck Lalloum, Laurent Laroche
Publikováno v:
Journal of cataract and refractive surgery. 34(9)
After uneventful phacoemulsification and in-the-bag implantation of an AcrySof SA60AT (Alcon) intraocular lens (IOL), a 52-year-old black man developed pigmentary glaucoma. Slitlamp examination, anterior segment optical coherence tomography, and ultr
Autor:
Veronique, Vieira, Gabriel, David, Olivier, Roche, Guillaume, de la Houssaye, Sandrine, Boutboul, Laurence, Arbogast, Alexandra, Kobetz, Christophe, Orssaud, Olivier, Camand, Daniel F, Schorderet, Francis, Munier, Annick, Rossi, Anne Lise, Delezoide, Cecile, Marsac, Daniel, Ricquier, Jean-Louis, Dufier, Maurice, Menasche, Marc, Abitbol
Publikováno v:
Molecular vision. 12
Axenfeld Rieger syndrome (ARS) is an autosomal dominant inherited disorder affecting development of the ocular anterior chamber, abdomen, teeth and facial structures. The PITX2 gene is a major gene encoding a major transcription factor associated wit
Autor:
Daniel F. Schorderet, Maurice Menasche, Francis L. Munier, Johnny Moore, Marc Abitbol, Laurent Laroche, Sandrine Boutboul, Janet Sinton, Graeme C.M. Black
Publikováno v:
Human mutation. 27(6)
Epithelial basement membrane corneal dystrophy (EBMD), also known as Cogan microcystic epithelial dystrophy or map-dot-fingerprint dystrophy, is a common bilateral epithelial dystrophy. Usually, this disease is not considered to be inherited although