Gimenez-Roqueplo AP - Search Results

1

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

Benn DE, Gimenez-Roqueplo AP, Reilly JR, Bertherat J, Burgess J, Byth K, Croxson M, Dahia PL, Elston M, Gimm O, Henley D, Herman P, Murday V, Niccoli-Sire P, Pasieka JL, Rohmer V, Tucker K, Jeunemaitre X, Marsh DJ, Plouin PF, Robinson BG. Benn DE, et al. J Clin Endocrinol Metab. 2006 Mar;91(3):827-36. doi: 10.1210/jc.2005-1862. Epub 2005 Nov 29. J Clin Endocrinol Metab. 2006. PMID: 16317055

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

[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.

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

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

7

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

8

[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.

9

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

10

[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.

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