Antignac C - Search Results

1

A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.

Antignac C, Arduy CH, Beckmann JS, Benessy F, Gros F, Medhioub M, Hildebrandt F, Dufier JL, Kleinknecht C, Broyer M, et al. Antignac C, et al. Nat Genet. 1993 Apr;3(4):342-5. doi: 10.1038/ng0493-342. Nat Genet. 1993. PMID: 7981755

2

Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragments.

Knebelmann B, Deschenes G, Gros F, Hors MC, Grünfeld JP, Zhou J, Tryggvason K, Gubler MC, Antignac C. Knebelmann B, et al. Among authors: antignac c. Am J Hum Genet. 1992 Jul;51(1):135-42. Am J Hum Genet. 1992. PMID: 1376965 Free PMC article.

3

Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen gene.

Antignac C, Zhou J, Sanak M, Cochat P, Roussel B, Deschênes G, Gros F, Knebelmann B, Hors-Cayla MC, Tryggvason K, et al. Antignac C, et al. Kidney Int. 1992 Nov;42(5):1178-83. doi: 10.1038/ki.1992.402. Kidney Int. 1992. PMID: 1453602 Free article.

4

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

Beckmann JS, Richard I, Hillaire D, Broux O, Antignac C, Bois E, Cann H, Cottingham RW Jr, Feingold N, Feingold J, et al. Beckmann JS, et al. Among authors: antignac c. C R Acad Sci III. 1991;312(4):141-8. C R Acad Sci III. 1991. PMID: 1901754

5

Renal functional reserve in children with reduced renal mass: study by two dietary periods.

Antignac C, Kindermans C, Dartois AM, Dechaux M, Broyer M, Kleinknecht C. Antignac C, et al. Pediatr Nephrol. 1990 Nov;4(6):607-13. doi: 10.1007/BF00858634. Pediatr Nephrol. 1990. PMID: 2088462 Clinical Trial.

6

[Kidney functional reserve. Studies in humans].

Kleinknecht C, Antignac C, Dechaux M, Dartois AM. Kleinknecht C, et al. Among authors: antignac c. Ann Pediatr (Paris). 1990 Feb;37(2):105-8. Ann Pediatr (Paris). 1990. PMID: 2181912 Review. French.

7

Delayed renal failure with extensive mesangiolysis following bone marrow transplantation.

Antignac C, Gubler MC, Leverger G, Broyer M, Habib R. Antignac C, et al. Kidney Int. 1989 Jun;35(6):1336-44. doi: 10.1038/ki.1989.132. Kidney Int. 1989. PMID: 2671466 Free article.

8

De novo membranous glomerulonephritis in renal allografts in children.

Antignac C, Hinglais N, Gubler MC, Gagnadoux MF, Broyer M, Habib R. Antignac C, et al. Clin Nephrol. 1988 Jul;30(1):1-7. Clin Nephrol. 1988. PMID: 3061691

9

Clinicopathological quiz. De novo membranous glomerulonephritis (MGN).

Antignac C, Broyer M, Hinglais N, Habib R. Antignac C, et al. Pediatr Nephrol. 1987 Oct;1(4):673-5. doi: 10.1007/BF00853608. Pediatr Nephrol. 1987. PMID: 3153350 No abstract available.

10

Toward the identification of a gene for familial juvenile nephronophthisis (autosomal recessive medullary cystic kidney disease).

Antignac C, Kleinknecht C, Habib R. Antignac C, et al. Adv Nephrol Necker Hosp. 1995;24:379-93. Adv Nephrol Necker Hosp. 1995. PMID: 7572421 Review. No abstract available.

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