Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Line Chevrette"'
Autor:
Rosanne Superstein, Ariane Milet, Julie Powell, Nicole Fallaha, François Codère, Line Chevrette, Rola Al Dhaybi, Patrick Hamel, Josée Dubois, Afshin Hatami, Catherine McCuaig, Luis H. Ospina
Publikováno v:
Ophthalmology. 118:1184-1188
Purpose To study the efficacy of propranolol in the treatment of periocular infantile hemangiomas (IHs). Design Retrospective interventional case series. Participants Eighteen children presenting periocular IH with occlusion of the pupil, anisometrop
Autor:
Line Chevrette, Magda Barsoum-Homsy, Barbara K. Teboul, Jean Milot, Isabelle Brunette, Michael G. Quigley, Jean-Louis Jacob, Robert C. Polomeno, Jacqueline Orquin
Publikováno v:
Ophthalmology. 102:1646-1653
Purpose: The purpose of this study is to determine the incidence of secondary hemorrhage after traumatic hyphema in children and to evaluate the efficacy of epsilon aminocaproic acid in reducing this incidence. Methods: In a prospective, randomized,
Autor:
Altaf Hossain, Mansoor Sarfarazi, M. Erol Turaçli, S. Gulderen Aktan, B. Sitki Sayli, Magda Barsoum-Homsy, Line Chevrette, A. Nurten Akarsu
Publikováno v:
American Journal of Medical Genetics. 61:290-292
Primary congenital glaucoma (gene symbol: GLC3) is characterized by an improper development of the aqueous outflow system. The reduced outflow of fluid results in an increased intraocular pressure leading to buphthalmos, optic nerve damage, and event
Autor:
Trushna Desai, Nehir Özdemir, Line Chevrette, D Stoilova, G Brice, R. Pitts Crick, A H Child, Mansoor Sarfarazi, M F Adam, Magda Barsoum-Homsy, H J Garchon
Publikováno v:
Journal of medical genetics. 35(12)
Mutations in the trabecular meshwork induced glucocorticoid response protein (TIGR) or myocilin (MYOC) has recently been shown to cause juvenile onset primary open angle glaucoma (JOAG). In this study, we identified two new mutations (Asp380Ala and S
Autor:
M E Turacli, M Or, G Brice, Miguel Coca-Prados, S G Aktan, Line Chevrette, R A Lewis, Anne H. Child, Ivaylo Stoilov, I Alozie, A N Akarsu, Magda Barsoum-Homsy, Mansoor Sarfarazi, Nehir Özdemir
PubMedID: 9497261 We recently reported three truncating mutations of the cytochrome P4501B1 gene (CYP1B1) in five families with primary congenital glaucoma (PCG) linked to the GLC3A locus on chromosome 2p21. This could be the first direct evidence su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f2db4b100f37152222081de0ec0e390
https://avesis.gazi.edu.tr/publication/details/9dbf4e30-6ee3-41a3-9035-c37d2b2d629f/oai
https://avesis.gazi.edu.tr/publication/details/9dbf4e30-6ee3-41a3-9035-c37d2b2d629f/oai
Publikováno v:
Ophthalmology. 104(12)
Objective: The authors investigated the temporal and spatial characteristics of pattern electroretinogram (PERG) and spatial contrast sensitivity (CS) in primary congenital glaucoma (PCG) to determine whether the PERG and CS could be useful tools in
Autor:
B. Sitki Sayli, A. Nurten Akarsu, S. Gulderen Aktan, Magda Barsoum-Homsy, Mansoor Sarfarazi, M. Erol Turaçli, Line Chevrette
Publikováno v:
Human molecular genetics. 5(8)
Primary congenital glaucoma (gene symbol: GLC3) is an ocular disorder that occurs for 0.01-0.04% of blind people. In the majority of familial cases reported so far, this condition is inherited as an autosomal recessive trait. We have recently used a
Autor:
A Hossain, Magda Barsoum-Homsy, Line Chevrette, B S Sayli, Mansoor Sarfarazi, S G Aktan, M E Turacli, A N Akarsu
Publikováno v:
Genomics. 30(2)
Primary congenital glaucoma (GLC3) is an inherited eye disorder that accounts for 0.01-0.04% of total blindness. Although a large number of chromosomal abnormalities have already been reported in patients with congenital glaucoma, the precise locatio
Autor:
Line Chevrette, Magda Barsoum-Homsy
Publikováno v:
Ophthalmology. 93:1323-1327
Sixty-three consecutive cases (95 eyes) of glaucoma in children were studied. Glaucoma associated with congenital anomalies (group II) formed the largest group in this study. This accounted for 46% of the cases compared to primary congenital glaucoma
Autor:
J. Navratil, Jean-Louis Jacob, Jacqueline Orquin, Jean Milot, Magda Barsoum-Homsy, Line Chevrette
Publikováno v:
American Orthoptic Journal. 38:135-141
The forced-preferential looking test has been shown to be an accurate method for assessment of monocular grating acuity in mentally retarded children. The current study seeks to validate the proced...