Zobrazeno 1 - 10
of 49
pro vyhledávání: '"L, Lasram"'
Autor:
R, Anane Touzri, B, Ben Romdhane, I, Mili Boussen, L, Kriaa, M, Ghattas, L, Lasram, R, Zhioua, A, Ouertani
Publikováno v:
La Tunisie medicale. 78(10)
The purpose of this study is to show the result of outpatient cataract surgery and its differences or advantages with inpatient cataract surgery.The retrospective study concern 722 consecutives patients collected from June 1995 till May 1997; 388 und
Publikováno v:
Nephrologie. 18(2)
We report on 24 children (10 girls) presenting with primary hyperoxaluria. The mean age at diagnosis was 6.3 years (range: 3 months-14.8 years). The mean interval between initial symptom and diagnosis was 1.3 year. The average follow-up period was 22
Publikováno v:
Journal francais d'ophtalmologie. 20(4)
To report the results of ophthalmological examination of 14 patients with primary oxalosis of type I, and to appreciate the diagnostic value of these signs.Fourteen patients, 7 girls and 7 boys with an average age of 8-35 years (3 months - 15 years).
Publikováno v:
Journal francais d'ophtalmologie. 17(5)
Leaking filtering blebs must be repaired immediately to avoid major complications such as hypotony and endophtalmitis. We report four cases of leaking filtering blebs occurring between one to six years after trabeculectomy. Revealing signs were hypot
Publikováno v:
Journal francais d'ophtalmologie. 17(4)
The authors reported ten cases of familial nephropathy (two cystinosis, three Senior and Loken syndrome, one Alport's syndrome and four Oxalosis) associated to ocular manifestations. Aetiologic diagnosis was known from ocular symptoms in five cases (
Publikováno v:
Journal francais d'ophtalmologie. 17(1)
Gelatinous drop-like corneal dystrophy is a rare disease, described for the first time by Nakaizumi (Japan) in 1914. We report 5 cases of this primary corneal amyloidosis. Three of our patients are brothers, the two other cases are isolated cases. Ph
Publikováno v:
Annales de dermatologie et de venereologie. 121(2)
A multidisciplinary transversal descriptive study was conducted from June to October 1992 to determine the clinical manifestations and laboratory findings observed in 66 patients with type 1 neurofibromatosis. Diagnostic criteria were those of the Na
Publikováno v:
La Tunisie medicale. 71(2)
Publikováno v:
La Tunisie medicale. 70(12)
Publikováno v:
Journal francais d'ophtalmologie. 15(2)
Aphthosis in Behçet's disease is usually located in the oro-genital areas, but other locations have been described. The authors report the case of a 45 year old woman who presented with an ocular conjunctival aphthous ulcer. This was the initial pre