Bacri Jl

[Renal botryomycosis. Clinicopathologic study of a case].

Arnaud François, Bacri Jl, J. P. Métayer, Jacques Hémet

Botryomycosis is a chronic bacterial infection characterized histologically by granules containing bacteria in microabscesses. Although Staphylococcus aureus is the most common causative agent, other bacteria have been reported to cause botryomycosis. Several factors have been hypothesized to be important in the pathogenesis …

fr (code pays fourni par la source)

[Intrafamilial renal transplantation in children after donor blood transfusions].

C. Kaplan, Patrick Niaudet, Gagnadoux Mf, Bacri Jl et autres

This article represents an update of our experience with deliberate donor specific blood transfusions (D.S.T.) prior to living-related renal transplantation in children. Eighteen recipients with a negative cross- match to donor T and B cells entered the D.S.T. protocol without regard to …

[Captopril treatment of arterial hypertension in children after renal transplantation].

Gagnadoux Mf, Corinne Antignac, Bacri Jl, Genevi�ve Guest et autres

52 children with renal allograft received captopril during 56 periods of treatment. High blood pressure (BP) was due to renal artery stenosis in 22 patients, to diffuse vascular lesions (mainly due to chronic rejection) in 13, to high-dose corticosteroid treatment in the …

[Results of kidney transplantation in children. Apropos of 213 grafts].

M Broyer, Gagnadoux Mf, D Beurton, D Gonthiez et autres

[Current aspects of the medical management of arterial hypertension in children].

Bacri Jl

[Is it necessary to biopsy the transplanted kidney as a rule?].

Micheline Lévy, Rocío López-García-Torres, AGNÈS BEZIAU, M Lacoste et autres

Aluminium encephalopathy: a potential risk of aluminium gels in children with chronic renal failure.

G Pillion, Chantel Loirat, Conrad B. Blum, Michel Poisson et autres

[Thyroid dysgenesis in mother and daughter].

Bacri Jl, GoT D, Job Jc

A case of congenital hypothyroidism with lingual thyroid in a woman and her daughter is presented. The scarcity of familial cases of thyroid malformations leads to discuss the genetic factors involved.