Zobrazeno 1 - 10
of 25
pro vyhledávání: '"K, Guedira"'
Publikováno v:
Neurochirurgie. 64:261
Introduction L’hematome extradural de la fosse cerebrale posterieure est une complication rare des traumatismes crâniens, en particulier en milieu pediatrique. Son pronostic, jadis grave, a ete nettement ameliore depuis l’avenement de la tomoden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f05e48510ca7c5671a6695b10e6503ac
https://doi.org/10.1016/j.neuchi.2018.05.126
https://doi.org/10.1016/j.neuchi.2018.05.126
Publikováno v:
Journal Français d'Ophtalmologie. 27:397-400
The Authors report a case of a 13-Year-old white child who presented a grade I hyphema, anterior chamber inflammation after trauma. He presented a secondary hemorrhage with increased intraocular pressure that was not controlled within 48 h, thus requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03b051cfb17dd73016e96bb1647f0aaf
https://doi.org/10.1016/s0181-5512(04)96148-7
https://doi.org/10.1016/s0181-5512(04)96148-7
Autor:
B, Tnacheri Ouazzani, K, Guedira, H, Dali, M, Laghmari, W, Ibrahimy, R, Daoudi, A, Sefiani, M, Chakir, M, Jiddane, Z, Mohcine
Publikováno v:
Journal francais d'ophtalmologie. 30(8)
Incontinentia pigmenti is a rare hereditary, dominant, X-linked disorder. It involves the skin, the teeth, the eyes and the central nervous system. The case we report is an infant girl aged 2 months. She had typical skin lesions associated with sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f084b4437f1e30bc9cdbf7474a640841
https://pubmed.ncbi.nlm.nih.gov/17978672
https://pubmed.ncbi.nlm.nih.gov/17978672
Publikováno v:
Journal francais d'ophtalmologie. 29(4)
Posterior microphthalmos with papillomacular fold is a rare disorder that involves both eyes without other ocular or systemic abnormalities. It is characterized by a short posterior segment with a normal anterior segment. We report the case of a 3.5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d014b18cc5d296cd2234d50c62ac1c2a
https://pubmed.ncbi.nlm.nih.gov/16885800
https://pubmed.ncbi.nlm.nih.gov/16885800
Publikováno v:
Journal francais d'ophtalmologie. 27(4)
The Authors report a case of a 13-Year-old white child who presented a grade I hyphema, anterior chamber inflammation after trauma. He presented a secondary hemorrhage with increased intraocular pressure that was not controlled within 48 h, thus requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b71c91e395504d9800c9ffd60ed09f0e
https://pubmed.ncbi.nlm.nih.gov/15173649
https://pubmed.ncbi.nlm.nih.gov/15173649
Publikováno v:
Journal francais d'ophtalmologie. 26(6)
Uveitis in children is rare: 3%-8% of all cases. It requires the same diagnostic and etiological processes as uveitis in adults, with additional difficulties at examination and a sometimes insidious progression.Retrospective study of 20 cases of chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::420ec8d358718820a9eedbb1b7c3f65e
https://pubmed.ncbi.nlm.nih.gov/12910201
https://pubmed.ncbi.nlm.nih.gov/12910201
Autor:
K, Guedira, N, Boutimzine, H, Karib, L, Dafrallah, A, Kabbaj, O, Cherkaoui, Z, Mohcine, F, Ezaitouni
Publikováno v:
Journal francais d'ophtalmologie. 23(7)
We describe a case of TINU Syndrome. A 17 year-old girl presented four weeks after an acute tubulo-interstitial nephritis with renal failure a bilateral anterior uveitis. Renal function improved spontaneously. Investigation failed to reveal systemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5c2f0339c71e8294c0e189b4a9d1013
https://pubmed.ncbi.nlm.nih.gov/10992068
https://pubmed.ncbi.nlm.nih.gov/10992068
Publikováno v:
Journal francais d'ophtalmologie. 23(5)
Neuromyelitis optical (NMO) or Devic's disease is an uncommon clinical syndrome associating unilateral or bilateral optic neuritis and transverse myelitis within about 8 weeks. Usually reported in adults, childhood cases constitute a distinctive clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70637b3b98f5fff7e8f3d03a18ac33fc
https://pubmed.ncbi.nlm.nih.gov/10844309
https://pubmed.ncbi.nlm.nih.gov/10844309
Autor:
N, Boutimzine, H, el Moussaif, M, Lezrek, A, Karim, L, Benzekri, K, Guedira, R, Daoudi, Z, Mohcine
Publikováno v:
Journal francais d'ophtalmologie. 21(6)
A 26 year-old woman, whose parents were consanguineously married, was admitted to our center because of bilateral juvenile cataract. The patient exhibited short stature, sclerodermalike appearance of the skin with a typical bird-like facies, thinning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::579c5e5996b6170571fa233a0e0c1f87
https://pubmed.ncbi.nlm.nih.gov/9759441
https://pubmed.ncbi.nlm.nih.gov/9759441
Autor:
Mina Laghmari, M. Chakir, M. Jiddane, K Guedira, W. Ibrahimy, Z. Mohcine, A. Sefiani, H. Dali, Rajae Daoudi, B. Tnacheri Ouazzani
Publikováno v:
Journal Français d'Ophtalmologie. 30:844.e1-844.e7
L’incontinentia pigmenti est une maladie genetique rare, a transmission dominante liee au chromosome X. Elle atteint la peau, les dents, mais aussi l’œil et le systeme nerveux central. Ces deux dernieres atteintes font la gravite de l’affectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac5400eac74b880632802a41d8ce3342
https://doi.org/10.1016/s0181-5512(07)92622-4
https://doi.org/10.1016/s0181-5512(07)92622-4