Broyer M - Search Results

1

Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.

Fuchshuber A, Niaudet P, Gribouval O, Jean G, Gubler MC, Broyer M, Antignac C. Fuchshuber A, et al. Among authors: broyer m. Pediatr Nephrol. 1996 Apr;10(2):135-8. doi: 10.1007/BF00862052. Pediatr Nephrol. 1996. PMID: 8703694

2

Cyclosporin in the treatment of idiopathic nephrotic syndrome in children.

Niaudet P, Habib R, Tete MJ, Hinglais N, Broyer M. Niaudet P, et al. Among authors: broyer m. Pediatr Nephrol. 1987 Oct;1(4):566-73. doi: 10.1007/BF00853590. Pediatr Nephrol. 1987. PMID: 3153333

3

Collagen type III glomerulopathy: a new type of hereditary nephropathy.

Gubler MC, Dommergues JP, Foulard M, Bensman A, Leroy JP, Broyer M, Habib R. Gubler MC, et al. Among authors: broyer m. Pediatr Nephrol. 1993 Aug;7(4):354-60. doi: 10.1007/BF00857536. Pediatr Nephrol. 1993. PMID: 8398640

4

Anti-OKT3 response following prophylactic treatment in paediatric kidney transplant recipients.

Niaudet P, Jean G, Broyer M, Chatenoud L. Niaudet P, et al. Among authors: broyer m. Pediatr Nephrol. 1993 Jun;7(3):263-7. doi: 10.1007/BF00853215. Pediatr Nephrol. 1993. PMID: 8518095

5

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

Fuchshuber A, Jean G, Gribouval O, Gubler MC, Broyer M, Beckmann JS, Niaudet P, Antignac C. Fuchshuber A, et al. Among authors: broyer m. Hum Mol Genet. 1995 Nov;4(11):2155-8. doi: 10.1093/hmg/4.11.2155. Hum Mol Genet. 1995. PMID: 8589695

6

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Jean G, Fuchshuber A, Town MM, Gribouval O, Schneider JA, Broyer M, van't Hoff W, Niaudet P, Antignac C. Jean G, et al. Among authors: broyer m. Am J Hum Genet. 1996 Mar;58(3):535-43. Am J Hum Genet. 1996. PMID: 8644713 Free PMC article.

7

Cyclosporine in the therapy of steroid-resistant idiopathic nephrotic syndrome.

Niaudet P, Fuchshuber A, Gagnadoux MF, Habib R, Broyer M. Niaudet P, et al. Among authors: broyer m. Kidney Int Suppl. 1997 Mar;58:S85-90. Kidney Int Suppl. 1997. PMID: 9067953 Review.

8

A controlled study of deflazacort in the treatment of idiopathic nephrotic syndrome.

Broyer M, Terzi F, Lehnert A, Gagnadoux MF, Guest G, Niaudet P. Broyer M, et al. Pediatr Nephrol. 1997 Aug;11(4):418-22. doi: 10.1007/s004670050308. Pediatr Nephrol. 1997. PMID: 9260237 Clinical Trial.

9

Familial juvenile nephronophthisis.

Konrad M, Saunier S, Calado J, Gubler MC, Broyer M, Antignac C. Konrad M, et al. Among authors: broyer m. J Mol Med (Berl). 1998 Apr;76(5):310-6. doi: 10.1007/s001090050222. J Mol Med (Berl). 1998. PMID: 9587065 Review.

10

[Genetics and nephrotic syndrome].

Niaudet P, Broyer M, Gubler MC, Jeanpierre C, Barbaux S, Antignac C. Niaudet P, et al. Among authors: broyer m. Arch Pediatr. 1998;5 Suppl 2:152s-155s. Arch Pediatr. 1998. PMID: 9759244 Review. French. No abstract available.

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