Zobrazeno 1 - 10
of 33
pro vyhledávání: '"N. Ghram"'
Publikováno v:
Archives de Pédiatrie. 6:1048-1052
Resume Ce travail a pour objectif de preciser la prevalence hospitaliere de cette maladie et de degager ses particularites cliniques et evolutives dans notre pays. Population Nous rapportons une etude retrospective de 15 cas de choree de Sydenham, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e7373807814461f8712f160880e9aff
https://doi.org/10.1016/s0929-693x(00)86977-8
https://doi.org/10.1016/s0929-693x(00)86977-8
Autor:
Azza Hammou, S. Ben Becher, T. Boudhina, Mondher Cheour, N. Ghram, S Hlioui, L. Ben Hassine, F. Houas
Publikováno v:
Archives de Pédiatrie. 4:1107-1110
Resume Les localisations cerebrales du kyste hydatique sont rares et s'observent surtout chez l'enfant en zone d'infestation endemique. Patients. — Six enfants âges de 4 a 8 ans et demi (âge moyen: 5 ans et demi) ont ete admis entre 1989 et 1994
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f671076bb7af6bfff108be23d0571334
https://doi.org/10.1016/s0929-693x(97)88979-8
https://doi.org/10.1016/s0929-693x(97)88979-8
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 6(10)
Sydenham's chorea was the most common form of acquired chorea in childhood. Its incidence has declined since the use of antibiotics. The aim of our study was to determine the hospital incidence of this disease and to illustrate the clinical character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::451be15dfcc9d68ca95c8f4706f38e2e
https://pubmed.ncbi.nlm.nih.gov/10544778
https://pubmed.ncbi.nlm.nih.gov/10544778
Autor:
S, Ben Becher, M, Cheour, L, Ben Hassine, S, Hlioui, F, Houas, N, Ghram, A, Hammou, T, Boudhina
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 4(11)
Brain cysts caused by Echinococcus granulosus are rare; they occur during childhood in endemic areas.Six children, aged to 8.5-years old (mean age: 5.5 years) were admitted from 1989 to 1994 because they suffered from progressive intracranial hyperte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5452f7bdaa94b04f78eb44c745a64b6
https://pubmed.ncbi.nlm.nih.gov/9488746
https://pubmed.ncbi.nlm.nih.gov/9488746
Publikováno v:
Archives francaises de pediatrie. 49(9)
Schwartz-Jampel syndrome is a rare disorder inherited as an autosomal recessive trait and characterized by growth retardation, multiple skeletal abnormalities, myotonia-like muscle disorders and unusual facies.Case n. 1: A boy, aged 3 years 4 months,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d238cb89a0049ae8f6f56190cf93dc7
https://pubmed.ncbi.nlm.nih.gov/1300968
https://pubmed.ncbi.nlm.nih.gov/1300968
Publikováno v:
Medecine tropicale : revue du Corps de sante colonial. 51(3)
The authors report the cases of five children in whom kala-azar was undiagnosed at first instance. In these cases, the diagnosis was misled because of incomplete features (lack of fever, splenomegaly or hypergammaglobulinemia) an associated disease (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5042338e4f8acb016fdf2bdc8ac6c082
https://pubmed.ncbi.nlm.nih.gov/1943639
https://pubmed.ncbi.nlm.nih.gov/1943639
Autor:
T, Boudhina, N, Ghram, S, Ben Becher, R, Lakhoua, R, Ayachi, A, Hammou-Jeddi, K, Ben Ghachem, B, Bennaceur, M, Hamza
Publikováno v:
Archives francaises de pediatrie. 48(4)
Seven cases of Budd-Chiari syndrome are reported in children. The mode of onset was fulminant in one case with rapidly lethal liver failure, acute in 5 cases with rapid appearance of hepatomegaly and ascites and insidious in one case, with isolated h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94029c63f38627b6303df8ba4a0bdf5c
https://pubmed.ncbi.nlm.nih.gov/2069474
https://pubmed.ncbi.nlm.nih.gov/2069474
Publikováno v:
Annales de pediatrie. 37(6)
We report the observations of three sisters with the same autosomal recessive syndrome characterized by growth retardation, microcephaly, mental deficiency, seizures, sensorineural hearing loss, and skin lesions. The congenital nature of these sympto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c04a8aed2076636c1f96effad287800e
https://pubmed.ncbi.nlm.nih.gov/2400194
https://pubmed.ncbi.nlm.nih.gov/2400194
Publikováno v:
La Tunisie medicale. 68(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b03dbf7f30d381e0c284baad3059e496
https://pubmed.ncbi.nlm.nih.gov/2309343
https://pubmed.ncbi.nlm.nih.gov/2309343
Publikováno v:
La Tunisie medicale. 66(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::febe1769fb0dc5b45a183701b8c546e5
https://pubmed.ncbi.nlm.nih.gov/3238781
https://pubmed.ncbi.nlm.nih.gov/3238781