Gimenez-Roqueplo AP - Search Results

1

Spectrum of mutations in Gitelman syndrome.

Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Vargas-Poussou R, et al. J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17. J Am Soc Nephrol. 2011. PMID: 21415153 Free PMC article.

2

Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel.

Corvol P, Persu A, Gimenez-Roqueplo AP, Jeunemaitre X. Corvol P, et al. Hypertension. 1999 Jun;33(6):1324-31. doi: 10.1161/01.hyp.33.6.1324. Hypertension. 1999. PMID: 10373210 Review.

3

Angiotensinogen variants and human hypertension.

Jeunemaitre X, Gimenez-Roqueplo AP, Célérier J, Corvol P. Jeunemaitre X, et al. Curr Hypertens Rep. 1999 Feb-Mar;1(1):31-41. doi: 10.1007/s11906-999-0071-0. Curr Hypertens Rep. 1999. PMID: 10981040 Review.

4

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway.

Gimenez-Roqueplo AP, Favier J, Rustin P, Mourad JJ, Plouin PF, Corvol P, Rötig A, Jeunemaitre X. Gimenez-Roqueplo AP, et al. Am J Hum Genet. 2001 Dec;69(6):1186-97. doi: 10.1086/324413. Epub 2001 Oct 16. Am J Hum Genet. 2001. PMID: 11605159 Free PMC article.

5

Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma.

Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Kerlan V, Plouin PF, Rötig A, Jeunemaitre X. Gimenez-Roqueplo AP, et al. J Clin Endocrinol Metab. 2002 Oct;87(10):4771-4. doi: 10.1210/jc.2002-020525. J Clin Endocrinol Metab. 2002. PMID: 12364472

6

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Crespin M, Nau V, Khau Van Kien P, Corvol P, Plouin PF, Jeunemaitre X; COMETE Network. Gimenez-Roqueplo AP, et al. Cancer Res. 2003 Sep 1;63(17):5615-21. Cancer Res. 2003. PMID: 14500403

7

[Genetics and arterial hypertension: 3 approaches to decode a complex disease].

Jeunemaitre X, Gimenez-Roqueplo AP. Jeunemaitre X, et al. Bull Acad Natl Med. 2002;186(9):1595-606; discussion 1606-9. Bull Acad Natl Med. 2002. PMID: 14556576 Review. French.

8

Evidence for carotid and radial artery wall subclinical lesions in renal fibromuscular dysplasia.

Boutouyrie P, Gimenez-Roqueplo AP, Fine E, Laloux B, Fiquet-Kempf B, Plouin PF, Jeunemaitre X, Laurent S. Boutouyrie P, et al. J Hypertens. 2003 Dec;21(12):2287-95. doi: 10.1097/00004872-200312000-00017. J Hypertens. 2003. PMID: 14654749

9

[Genetics and essential hypertension: candidate genes or screening of the whole genome?].

Gimenez-Roqueplo AP, Jeunemaitre X. Gimenez-Roqueplo AP, et al. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1089-95. Arch Mal Coeur Vaiss. 2003. PMID: 14694785 Review. French.

10

Juvenile hemochromatosis HJV-related revealed by cardiogenic shock.

Filali M, Le Jeunne C, Durand E, Grinda JM, Roetto A, Daraio F, Bruneval P, Jeunemaitre X, Gimenez-Roqueplo AP. Filali M, et al. Blood Cells Mol Dis. 2004 Sep-Oct;33(2):120-4. doi: 10.1016/j.bcmd.2004.05.001. Blood Cells Mol Dis. 2004. PMID: 15315789

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