Michel Broyer

Delayed renal failure with extensive mesangiolysis following bone marrow transplantation.

G. Leverger, C. Antignac, M. Gubler, 1989, Kidney international.

Haemolytic uraemic syndrome: prognostic factors in children over 3 years of age

P. Niaudet, M. Broyer, R. Habib, 1995, Pediatric Nephrology.

Membranous glomerulonephritis and hepatitis B surface antigen in children.

M. Lévy, M. Broyer, A. Peix, 1979, The Journal of pediatrics.

Evaluation in patients with Alport syndrome of knowledge of the disease and attitudes toward prenatal diagnosis.

B. Boudailliez, Y. Pirson, A. Moynot, 1994, Clinical nephrology.

Alterations of protein metabolism by metabolic acidosis in children with chronic renal failure.

Y. Boirie, P. Niaudet, J. Bresson, 2000, Kidney international.

PAX2 mutations in oligomeganephronia.

S. Lyonnet, M. Gubler, M. Vekemans, 2001, Kidney international.

Collagen type III glomerulopathy: a new type of hereditary nephropathy

M. Gubler, A. Bensman, J. Leroy, 1993, Pediatric Nephrology.