Zobrazeno 1 - 10
of 223
pro vyhledávání: '"F. Hayem"'
Autor:
F., Hayem
Publikováno v:
In Archives de pédiatrie 2002 9(6):638-643
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology. 78:594-598
Diffuse sclerosing osteomyelitis of the mandible has been described as a localized disease of unknown origin. We offer evidence that mandibular involvement in the recently described synovitis acne pustulosis hyperostosis osteitis syndrome exactly fit
Publikováno v:
Journal de Pédiatrie et de Puériculture. 13:287-289
Les arthrites chroniques juveniles (ACJ) forment un groupe clinique heterogene dont la prevalence est estimee en France de 7 a 10/100 000 [11]. L'atteinte articulaire, denominateur commun aux differentes formes de la maladie, reste l'element principa
Autor:
F, Hayem
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9(6)
Periodic fever is defined as a series of unexplained febrile episodes, most often starting during childhood. The febrile episodes last usually few days, are of fixed or variable duration, and regress spontaneously, the intervals between episodes bein
Autor:
F, Hayem
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 7(8)
Autor:
F, Hayem
Publikováno v:
Revue du rhumatisme (English ed.). 66(10)
Publikováno v:
The Journal of rheumatology. 23(7)
Publikováno v:
Revue du rhumatisme (English ed.). 63(1)
Long term prognosis of systemic juvenile chronic arthritis range from full recovery to extremely severe crippling polyarthritis. An association between HLA-DR4 and a poor articular outcome has been reported. We studied the frequencies of class I, cla
Publikováno v:
Annales de dermatologie et de venereologie. 123(1)
Blau syndrome is a granulomatous disease with dominant autosomal transmission. Skin, joint and ocular manifestations usually appear in childhood.A father and his son had granulomatous disease with skin and joint manifestations beginning in childhood.
Publikováno v:
Revue du rhumatisme (Ed. francaise : 1993). 61(9)
The objective of this work was to evaluate the course of hip disease in patients with systemic-onset juvenile chronic arthritis. 59 patients with systemic-onset juvenile chronic arthritis followed-up for a mean of 15 years (+/- 6 years) were studied