Clément K - Search Results

1

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction.

Clément K, Vaisse C, Lahlou N, Cabrol S, Pelloux V, Cassuto D, Gourmelen M, Dina C, Chambaz J, Lacorte JM, Basdevant A, Bougnères P, Lebouc Y, Froguel P, Guy-Grand B. Clément K, et al. Nature. 1998 Mar 26;392(6674):398-401. doi: 10.1038/32911. Nature. 1998. PMID: 9537324

2

Primary pancreatic beta-cell secretory defect caused by mutations in glucokinase gene in kindreds of maturity onset diabetes of the young.

Velho G, Froguel P, Clement K, Pueyo ME, Rakotoambinina B, Zouali H, Passa P, Cohen D, Robert JJ. Velho G, et al. Among authors: clement k. Lancet. 1992 Aug 22;340(8817):444-8. doi: 10.1016/0140-6736(92)91768-4. Lancet. 1992. PMID: 1354782

3

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.

Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, et al. Froguel P, et al. Among authors: clement k. Nature. 1992 Mar 12;356(6365):162-4. doi: 10.1038/356162a0. Nature. 1992. PMID: 1545870

4

Genetic variation in the beta 3-adrenergic receptor and an increased capacity to gain weight in patients with morbid obesity.

Clément K, Vaisse C, Manning BS, Basdevant A, Guy-Grand B, Ruiz J, Silver KD, Shuldiner AR, Froguel P, Strosberg AD. Clément K, et al. N Engl J Med. 1995 Aug 10;333(6):352-4. doi: 10.1056/NEJM199508103330605. N Engl J Med. 1995. PMID: 7609752 Free article.

5

[Lipo-atrophic diabetes, "a rare disease of adipocytes?"].

Clément K, Basdevant A, Guy-Grand B. Clément K, et al. Rev Prat. 1994 May 15;44(10):1329-32. Rev Prat. 1994. PMID: 7939193 French. No abstract available.

6

Arginine-induced insulin release in glucokinase-deficient subjects.

Pueyo ME, Clement K, Vaxillaire M, Passa P, Froguel P, Robert JJ, Velho G. Pueyo ME, et al. Among authors: clement k. Diabetes Care. 1994 Sep;17(9):1015-21. doi: 10.2337/diacare.17.9.1015. Diabetes Care. 1994. PMID: 7988299

7

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.

Velho G, Byrne MM, Clément K, Sturis J, Pueyo ME, Blanché H, Vionnet N, Fiet J, Passa P, Robert JJ, Polonsky KS, Froguel P. Velho G, et al. Among authors: clement k. Diabetes. 1996 Apr;45(4):478-87. doi: 10.2337/diab.45.4.478. Diabetes. 1996. PMID: 8603770

8

Indication for linkage of the human OB gene region with extreme obesity.

Clement K, Garner C, Hager J, Philippi A, LeDuc C, Carey A, Harris TJ, Jury C, Cardon LR, Basdevant A, Demenais F, Guy-Grand B, North M, Froguel P. Clement K, et al. Diabetes. 1996 May;45(5):687-90. doi: 10.2337/diab.45.5.687. Diabetes. 1996. PMID: 8621024

9

Candidate gene approach of familial morbid obesity: linkage analysis of the glucocorticoid receptor gene.

Clément K, Philippi A, Jury C, Pividal R, Hager J, Demenais F, Basdevant A, Guy-Grand B, Froguel P. Clément K, et al. Int J Obes Relat Metab Disord. 1996 Jun;20(6):507-12. Int J Obes Relat Metab Disord. 1996. PMID: 8782725

10

Additive effect of A-->G (-3826) variant of the uncoupling protein gene and the Trp64Arg mutation of the beta 3-adrenergic receptor gene on weight gain in morbid obesity.

Clément K, Ruiz J, Cassard-Doulcier AM, Bouillaud F, Ricquier D, Basdevant A, Guy-Grand B, Froguel P. Clément K, et al. Int J Obes Relat Metab Disord. 1996 Dec;20(12):1062-6. Int J Obes Relat Metab Disord. 1996. PMID: 8968850

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