Antignac C - Search Results

1

A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS.

Huynh Cong E, Bizet AA, Boyer O, Woerner S, Gribouval O, Filhol E, Arrondel C, Thomas S, Silbermann F, Canaud G, Hachicha J, Ben Dhia N, Peraldi MN, Harzallah K, Iftene D, Daniel L, Willems M, Noel LH, Bole-Feysot C, Nitschké P, Gubler MC, Mollet G, Saunier S, Antignac C. Huynh Cong E, et al. Among authors: antignac c. J Am Soc Nephrol. 2014 Nov;25(11):2435-43. doi: 10.1681/ASN.2013101126. Epub 2014 May 29. J Am Soc Nephrol. 2014. PMID: 24876116 Free PMC article.

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

[Congenital or childhood nephrotic syndrome with diffuse mesangial sclerosis].

Habib R, Gubler MC, Antignac C, Loirat C, Gangnadoux MF. Habib R, et al. Among authors: antignac c. Ann Pediatr (Paris). 1990 Feb;37(2):73-7. Ann Pediatr (Paris). 1990. PMID: 2157355 Review. French.

4

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.

5

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

6

Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.

Gubler MC, Knebelmann B, Beziau A, Broyer M, Pirson Y, Haddoum F, Kleppel MM, Antignac C. Gubler MC, et al. Among authors: antignac c. Kidney Int. 1995 Apr;47(4):1142-7. doi: 10.1038/ki.1995.163. Kidney Int. 1995. PMID: 7783412 Free article.

7

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

Medhioub M, Cherif D, Benessy F, Silbermann F, Gubler MC, Le Paslier D, Cohen D, Weissenbach J, Beckmann J, Antignac C. Medhioub M, et al. Among authors: antignac c. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

8

A specific glomerular lesion of the graft: allograft glomerulopathy.

Habib R, Zurowska A, Hinglais N, Gubler MC, Antignac C, Niaudet P, Broyer M, Gagnadoux MF. Habib R, et al. Among authors: antignac c. Kidney Int Suppl. 1993 Jul;42:S104-11. Kidney Int Suppl. 1993. PMID: 8361120

9

Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

Habib R, Gubler MC, Antignac C, Gagnadoux MF. Habib R, et al. Among authors: antignac c. Adv Nephrol Necker Hosp. 1993;22:43-57. Adv Nephrol Necker Hosp. 1993. PMID: 8381254 Review. No abstract available.

10

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.

Gubler MC, Antignac C, Deschênes G, Knebelmann B, Hors-Cayla MC, Grünfeld JP, Broyer M, Habib R. Gubler MC, et al. Among authors: antignac c. Adv Nephrol Necker Hosp. 1993;22:15-35. Adv Nephrol Necker Hosp. 1993. PMID: 8427057 Review. No abstract available.

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