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Items: 5

1.

A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.

Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, B├╝chler M, Cochat P, Cosyns JP, Mougenot B, Rider MH, Antignac C, Verellen-Dumoulin C, Pirson Y.

J Am Soc Nephrol. 2003 Nov;14(11):2883-93.

2.

Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: two facets of the same disease?

Dahan K, Fuchshuber A, Adamis S, Smaers M, Kroiss S, Loute G, Cosyns JP, Hildebrandt F, Verellen-Dumoulin C, Pirson Y.

J Am Soc Nephrol. 2001 Nov;12(11):2348-57.

3.

Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindreds.

Walon C, Kartheuser A, Michils G, Smaers M, Lannoy N, Ngounou P, Mertens G, Verellen-Dumoulin C.

Hum Genet. 1997 Oct;100(5-6):601-5.

PMID:
9341879
4.

The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screening.

Kartheuser A, West S, Walon C, Curtis A, Hamzehloei T, Lannoy N, Michiels G, Smaers M, Chapman P, Burn J, et al.

Acta Gastroenterol Belg. 1995 Sep-Dec;58(5-6):433-51. Review.

PMID:
8776001
5.

[Socioeconomic aspects of renal transplantation].

Kinnaert P, Van Haelewyck B, Smaers M, Vanherweghem JL, Vereerstraeten P, Toussaint C.

Rev Med Brux. 1984 May;5(5):339-42. French. No abstract available.

PMID:
6379808

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