Zobrazeno 1 - 10
of 105
pro vyhledávání: '"T, Boudhina"'
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
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 de pediatrie : organe officiel de la Societe francaise de pediatrie. 4(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::879e7f55b14042f9893e13f4700d0dac
https://pubmed.ncbi.nlm.nih.gov/9239277
https://pubmed.ncbi.nlm.nih.gov/9239277
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 1(12)
The spectrum of CHARGE association includes coloboma, heart disease, choanal atresia, retarded growth and development and/or CNS anomalies, genital anomalies and/or hypogonadism and ear anomalies and/or deafness.A 4 1/2 month-old boy was admitted suf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::76c0b288e3ddca6a76f40d5f5ed6bd99
https://pubmed.ncbi.nlm.nih.gov/7849898
https://pubmed.ncbi.nlm.nih.gov/7849898
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 1(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71ea4421d83b00eed69d7ff5e66cb4f6
https://pubmed.ncbi.nlm.nih.gov/7951841
https://pubmed.ncbi.nlm.nih.gov/7951841
Publikováno v:
Archives francaises de pediatrie. 50(7)
Proteus syndrome is characterized by a range of various manifestations. The main ones are partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly. Urinary tract abnormalities are exceptional.A 6 year-old boy was examined because he h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a2ec9d76421a01dfd22c0083dbfdde18
https://pubmed.ncbi.nlm.nih.gov/8002726
https://pubmed.ncbi.nlm.nih.gov/8002726
Publikováno v:
Archives francaises de pediatrie. 50(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e499c379b77c2b4f95da6164aad6fe5
https://pubmed.ncbi.nlm.nih.gov/8507142
https://pubmed.ncbi.nlm.nih.gov/8507142
Publikováno v:
Pediatrie. 48(1)
We report on a case of dermatitis herpetiformis in an eight-year-old boy presenting diarrhoea, short stature and characteristic skin rash. Jejunal biopsy showed a partial villous atrophy. The diagnosis was confirmed by immunofluorescence which showed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92f5122282c9698a449ad478d357d19f
https://pubmed.ncbi.nlm.nih.gov/8392692
https://pubmed.ncbi.nlm.nih.gov/8392692
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:
Annales de pediatrie. 39(5)
Tumor-like calcinosis is an infrequent condition whose etiology is poorly understood. Calcifications develop in the subcutaneous tissue neighboring the large joints. All age groups can be affected, although the disease is more common before the age o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::41f4132e7ab16e7336dcca92b70172fd
https://pubmed.ncbi.nlm.nih.gov/1616249
https://pubmed.ncbi.nlm.nih.gov/1616249