Zobrazeno 1 - 10
of 417
pro vyhledávání: '"Dominique, Bremond"'
Autor:
Giulia Marchione, Alejandra Daruich, Matthieu P. Robert, Dominique Bremond-Gignac, Sophie Valleix
Publikováno v:
JFO Open Ophthalmology, Vol 9, Iss , Pp 100147- (2025)
Externí odkaz:
https://doaj.org/article/b004c299f9c34ada814853171a8904c3
Autor:
Dominique Bremond-Gignac
Publikováno v:
Frontiers in Ophthalmology, Vol 4 (2024)
Externí odkaz:
https://doaj.org/article/61801557a3f74db3a5b4217d85a08d7f
Akademický článek
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Autor:
Ariel Beresniak, Christian Napoli, John Oxford, Alejandra Daruich, Laurent Niddam, Gérard Duru, Alberto E. Tozzi, Marta Ciofi degli Atti, Danielle Dupont, Caterina Rizzo, Dominique Bremond-Gignac
Publikováno v:
Cost Effectiveness and Resource Allocation, Vol 21, Iss 1, Pp 1-12 (2023)
Abstract Background The FLURESP project is a public health research funded by the European Commission, with the objective to design a methodological framework to assess the cost-effectiveness of existing public health measures against human influenza
Externí odkaz:
https://doaj.org/article/9d5e2d32e0ff4174a782671a3ccfd9e3
Autor:
Annegret Dahlmann-Noor, Stefano Bonini, Dominique Bremond-Gignac, Steffen Heegaard, Andrea Leonardi, Jesús Montero, Eduardo D. Silva, The EUR-VKC Group
Publikováno v:
Ophthalmology and Therapy, Vol 12, Iss 2, Pp 1207-1222 (2023)
Plain Language Summary Vernal keratoconjunctivitis (VKC) is a rare, underdiagnosed, chronic allergic eye disease that typically occurs in children and adolescents. If left untreated, VKC can significantly damage the eye, potentially leading to long-t
Externí odkaz:
https://doaj.org/article/7a7dde36901b4ce8b1906fce34fe3470
Autor:
Gorka Fernández-Eulate, Gilles C. Martin, Pascal Dureau, Claude Speeg-Spatz, Anais Brassier, Perrine Gillard, Dominique Bremond-Gignac, Dominique Thouvenin, Cecile Pagan, Foudil Lamari, Yann Nadjar
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-6 (2022)
Abstract Background Cerebrotendinous xanthomatosis (CTX) is a rare genetic disorder related to CYP27A1 biallelic mutations, leading to decreased synthesis of bile acids and increased cholestanol. Juvenile bilateral cataracts are one of the most commo
Externí odkaz:
https://doaj.org/article/d3cb3bd6df1b496293971bd9fcb2ed7b
Publikováno v:
Frontiers in Ophthalmology, Vol 3 (2023)
Genetic pediatric eye disease frequently leads to severe vision impairment or blindness. Voretigene neparvovec is the first approved gene therapy for an inherited retinal dystrophy (IRD). Voretigene neparvovec has been shown to be well tolerated and
Externí odkaz:
https://doaj.org/article/3da044043be34162baa65b0e27697a51
Autor:
Malika Foy, Philippe deMazancourt, Dominique Bremond Gignac, Fabrice Gillas, Nawel Trigui, Ahmed Mekki, Robert Carlier, Karelle Benistan
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract We described a novel de novo missense variant of the gene encoding Collagen alpha‐2(V) chain, associated with the classical Ehlers–Danlos syndrome (cEDS) (OMIM#130010), in a 14‐year‐old patient who presented with congenital and sever
Externí odkaz:
https://doaj.org/article/55177b8865a34caf8d28f756301e46df
Autor:
Jodhbir S. Mehta, Wei-Li Chen, Arthur C. K. Cheng, Le Xuan Cung, Ivo J. Dualan, Ramesh Kekunnaya, Nurliza Khaliddin, Tae-Im Kim, Douglas K. Lam, Seo Wei Leo, Florence Manurung, Nattaporn Tesavibul, Dominique Bremond-Gignac
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Vernal keratoconjunctivitis (VKC) is an underdiagnosed and underrecognized ocular surface disease with limited epidemiological data in Asia. It is more prevalent in warm, dry, and windy climates, and often has a substantial impact on a patient’s qu
Externí odkaz:
https://doaj.org/article/6290e9c72e1546ceb7ba372e476f4fd3
Autor:
Olivia Xerri, Federico Bernabei, Elise Philippakis, Cyril Burin-Des-Roziers, Pierre-Olivier Barale, Olivier Laplace, Claire Monin, Dominique Bremond-Gignac, Gilles Guerrier, Sophie Valleix, Antoine Brezin, Pierre-Raphaël Rothschild
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background To compare different clinical and Spectral-Domain Optical Coherence Tomography (SD-OCT) features of high myopic eyes with Stickler syndrome (STL) with matched controls. Methods Patients with genetically confirmed STL with axial le
Externí odkaz:
https://doaj.org/article/7e160eca8d5a449b8c7c234e8b224cb6