Gimenez-Roqueplo AP - Search Results

1

TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma.

Abermil N, Guillaud-Bataille M, Burnichon N, Venisse A, Manivet P, Guignat L, Drui D, Chupin M, Josseaume C, Affres H, Plouin PF, Bertherat J, Jeunemaître X, Gimenez-Roqueplo AP. Abermil N, et al. J Clin Endocrinol Metab. 2012 May;97(5):E805-9. doi: 10.1210/jc.2011-3360. Epub 2012 Mar 14. J Clin Endocrinol Metab. 2012. PMID: 22419703

2

Selective recognition of M235T angiotensinogen variants and their determination in human plasma by monoclonal antibody-based immunoanalysis.

Cohen P, Badouaille G, Gimenez-Roqueplo AP, Mani JC, Guyene TT, Jeunemaitre X, Menard J, Corvol P, Pau B, Simon D. Cohen P, et al. J Clin Endocrinol Metab. 1996 Oct;81(10):3505-12. doi: 10.1210/jcem.81.10.8855793. J Clin Endocrinol Metab. 1996. PMID: 8855793

3

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.

4

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.

5

[Recent progress in the diagnosis, prognostic evaluation and treatment of pheochromocytomas].

Plouin PF, Gimenez-Roqueplo AP, La Batide Alanore A, Salenave S, Duclos JM. Plouin PF, et al. Rev Med Interne. 2000 Dec;21(12):1075-85. doi: 10.1016/s0248-8663(00)00268-x. Rev Med Interne. 2000. PMID: 11191675 Review. French.

6

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.

7

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

8

Effects of slow-release octreotide on urinary metanephrine excretion and plasma chromogranin A and catecholamine levels in patients with malignant or recurrent phaeochromocytoma.

Lamarre-Cliche M, Gimenez-Roqueplo AP, Billaud E, Baudin E, Luton JP, Plouin PF. Lamarre-Cliche M, et al. Clin Endocrinol (Oxf). 2002 Nov;57(5):629-34. doi: 10.1046/j.1365-2265.2002.01658.x. Clin Endocrinol (Oxf). 2002. PMID: 12390337

9

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

10

[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.

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