Zobrazeno 1 - 10
of 60
pro vyhledávání: '"N, Laouissi"'
Autor:
M. Belhadji, R. Rachid, N Laouissi, M. Hamdani, D. Lahbil, A. Amraoui, M Wafi, K. Zaghloul, L. Rais
Publikováno v:
Journal Français d'Ophtalmologie. 27:801-804
La hyalopathie asteroide est une degenerescence vitreenne rare. Son association a une retinopathie pigmentaire est exceptionnelle. Nous rapportons le cas d'un homme de 65 ans, qui s'est presente en consultation pour une hemeralopie evoluant depuis l'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b13f8993aa9963e8dcad4a3a6016208
https://doi.org/10.1016/s0181-5512(04)96217-1
https://doi.org/10.1016/s0181-5512(04)96217-1
Autor:
N Laouissi, S. Benamour, K. Zaghloul, O. Benchekroun, D. Lahbil, M. El Belhadji, A. Amraoui, R. Rachid, H. Lamari
Publikováno v:
Journal Français d'Ophtalmologie. 27:154-159
Introduction L’atteinte maculaire n’est pas une manifestation classique de la maladie de Behcet ; cependant, son pronostic reserve justifie son interet. But du travail Le but de ce travail est de determiner la frequence de ces maculopathies, de d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4df873a075e2bbcc29a1c3d4de4ecfbf
https://doi.org/10.1016/s0181-5512(04)96110-4
https://doi.org/10.1016/s0181-5512(04)96110-4
Autor:
M, Wafi, L, Raïs, D, Lahbil, M, Hamdani, R, Rachid, M, Belhadji, N, Laouissi, K, Zaghloul, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 27(7)
Asteroid hyalosis is a rare degenerative condition of the vitreous. No causal relationship between retinitis pigmentosa and asteroid hyalosis has been established. We report a case of a 65-year-old male admitted for progressive hemeralopia. Visual ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d7d89fb893339633342eed0e441192c0
https://pubmed.ncbi.nlm.nih.gov/15499279
https://pubmed.ncbi.nlm.nih.gov/15499279
Autor:
O, Benchekroun, D, Lahbil, H, Lamari, R, Rachid, M, El Belhadji, N, Laouissi, K, Zaghloul, S, Benamour, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 27(2)
The macular damage in Behçet's disease requires particular attention because of its poor prognosis.The purpose of our study was to specify the frequency of macular alterations in Behçet's disease and discuss the clinical, physiopathological and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cae03cb7a186bb3e88604d08f7d455e5
https://pubmed.ncbi.nlm.nih.gov/15029043
https://pubmed.ncbi.nlm.nih.gov/15029043
Autor:
L, Rais, M, Wafi, D, Lahbil, M, Iraki, J, Fekkak, M, Hamdani, W, Benchekroun, R, Rachid, M, Belhadji, N, Laouissi, K, Zaghloul, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 26(10)
Homocystinuria is an autosomal recessive disorder of methionine metabolism due to cystathionine B-synthetase deficiency. It is the second most common inborn error of amino acid metabolism after phenylketonuria. In addition to the eyes, the skeletal,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::521c7a08e4569477529bd90cb5de4df3
https://pubmed.ncbi.nlm.nih.gov/14691398
https://pubmed.ncbi.nlm.nih.gov/14691398
Publikováno v:
Journal francais d'ophtalmologie. 25(9)
Membranoproliferative glomerulonephritis type II (MPGN) is characterized by dense deposits within glomerular basal membrane and Bruch's membrane which result in retinal lesions similar to drusens. We observed a 50-year-old patient with chronic renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c167960640b3f8390ab4c1d90827f3b
https://pubmed.ncbi.nlm.nih.gov/12515943
https://pubmed.ncbi.nlm.nih.gov/12515943
Autor:
A, el Kettani, M, Hamdani, L, Rais, M, el Belhadji, R, Rachid, N, Laouissi, K, Zaghloul, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 24(9)
Weill Marchesani syndrome is a congenital disease that combines microspherophakia and skeletal abnormalities. The authors report a 19-year-old male, born of a consanguineous marriage, with a progressive decrease in visual acuity. The general examinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c0d3ac94dc59120f8343fcc6cd0829f
https://pubmed.ncbi.nlm.nih.gov/11912838
https://pubmed.ncbi.nlm.nih.gov/11912838
Autor:
M, Hamdani, A, El Kettani, L, Rais, M, El Belhadji, R, Rachid, N, Laouissi, K, Zaghloul, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 23(8)
Juvenile xanthogranuloma (JXG) is a rare and usually benign disease occurring in early childhood. It causes skin and deep seated lesions, notably in the eye. We report a case of JXG in the iris of a 9-month-old infant. Examination under general anest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc820bf13ee00a3cf41ab44ec93708e4
https://pubmed.ncbi.nlm.nih.gov/11033505
https://pubmed.ncbi.nlm.nih.gov/11033505
Autor:
D, Lahbil, M, Hamdani, M, D'khissy, M, El Belhadji, R, Rachid, N, Laouissi, K, Zaghloul, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 23(8)
Gyrate atrophy of the retina and choroid is a rare disease, with recessive autosomal transmission, characterized by progressive chorioretinal atrophy causing blindness. It results from a congenital deficit in aminotransferase ornithine.The authors pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5a46ca5f5670a72b08dce1193dc4847
https://pubmed.ncbi.nlm.nih.gov/11033500
https://pubmed.ncbi.nlm.nih.gov/11033500
Autor:
Y, El Mansouri, F H, Kadiri, A, Saidi, N, Laouissi, K, Zaghloul, A, Idrissi Chekkoury, Y, Benchakroun, A, Amraoui
Publikováno v:
Journal francais d'ophtalmologie. 23(5)
Fractures of the orbit floor have very disabling oculomotor after effects. The objective of this study was to report that close collaboration between the maxillo-facial specialist and ophthalmologist is necessary to avoid oculomotor after effects.Our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2b3140c37463581b50dd81b9a762d09
https://pubmed.ncbi.nlm.nih.gov/10844302
https://pubmed.ncbi.nlm.nih.gov/10844302