Persu A - Search Results

1

Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an update.

Persu A, Lannoy N, Maiter D, Mendola A, Montigny P, Oriot P, Vinck W, Garin P, Hamoir M, Vikkula M. Persu A, et al. Horm Metab Res. 2012 May;44(5):349-53. doi: 10.1055/s-0032-1311610. Epub 2012 May 7. Horm Metab Res. 2012. PMID: 22566194

2

Hereditary paraganglioma.

Lemaire M, Persu A, Hainaut P, De Plaen JF. Lemaire M, et al. Among authors: persu a. J Intern Med. 1999 Jul;246(1):113-6. doi: 10.1046/j.1365-2796.1999.00519.x. J Intern Med. 1999. PMID: 10447233 Free article.

3

CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease.

Persu A, Devuyst O, Lannoy N, Materne R, Brosnahan G, Gabow PA, Pirson Y, Verellen-Dumoulin C. Persu A, et al. J Am Soc Nephrol. 2000 Dec;11(12):2285-2296. doi: 10.1681/ASN.V11122285. J Am Soc Nephrol. 2000. PMID: 11095651

4

Influence of the endothelial nitric oxide synthase gene on conventional and ambulatory blood pressure: sib-pair analysis and haplotype study.

Persu A, Vinck WJ, El Khattabi O, Janssen RG, Paulussen AD, Devuyst O, Vlietinck R, Fagard RH. Persu A, et al. J Hypertens. 2005 Apr;23(4):759-65. doi: 10.1097/01.hjh.0000163144.74588.ad. J Hypertens. 2005. PMID: 15775780

5

Cardiovascular risk assessment in hypertensive patients: major discrepancy according to ESH and SCORE strategies.

Lengelé JP, Vinck WJ, De Plaen JF, Persu A. Lengelé JP, et al. Among authors: persu a. J Hypertens. 2007 Apr;25(4):757-62. doi: 10.1097/HJH.0b013e328017f6fa. J Hypertens. 2007. PMID: 17351366

6

High prevalence of SDHB mutations in head and neck paraganglioma in Belgium.

Persu A, Hamoir M, Grégoire V, Garin P, Duvivier E, Reychler H, Chantrain G, Mortier G, Mourad M, Maiter D, Vikkula M. Persu A, et al. J Hypertens. 2008 Jul;26(7):1395-401. doi: 10.1097/HJH.0b013e3282ffdc54. J Hypertens. 2008. PMID: 18551016

7

Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity.

Persu A, Amyere M, Gutierrez-Roelens I, Rustin P, Sempoux C, Lecouvet FE, Van Beers BE, Horsmans Y, De Plaen JF, MarcHamoir, Vikkula M. Persu A, et al. J Hypertens. 2009 Jan;27(1):76-82. doi: 10.1097/hjh.0b013e328317a777. J Hypertens. 2009. PMID: 19145771

8

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

Yao L, Schiavi F, Cascon A, Qin Y, Inglada-Pérez L, King EE, Toledo RA, Ercolino T, Rapizzi E, Ricketts CJ, Mori L, Giacchè M, Mendola A, Taschin E, Boaretto F, Loli P, Iacobone M, Rossi GP, Biondi B, Lima-Junior JV, Kater CE, Bex M, Vikkula M, Grossman AB, Gruber SB, Barontini M, Persu A, Castellano M, Toledo SP, Maher ER, Mannelli M, Opocher G, Robledo M, Dahia PL. Yao L, et al. Among authors: persu a. JAMA. 2010 Dec 15;304(23):2611-9. doi: 10.1001/jama.2010.1830. JAMA. 2010. PMID: 21156949 Free article.

9

A genome-wide association study-derived candidate gene seeks replication: STK39.

Persu A, Vikkula M. Persu A, et al. J Hypertens. 2011 Mar;29(3):434-6. doi: 10.1097/HJH.0b013e328344b6b3. J Hypertens. 2011. PMID: 21317723 No abstract available.

10

Two-site automated chemiluminescent assay for measurement of immunoreactive renin.

Gruson D, Maisin D, Lison P, Maiter D, Persu A. Gruson D, et al. Among authors: persu a. Biomarkers. 2011 Nov;16(7):605-9. doi: 10.3109/1354750X.2011.614015. Biomarkers. 2011. PMID: 22022827

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