1. 1A.01: MUTATIONS AFFECTING THE CONSERVED ACIDIC MOTIF OF WNK1 CAUSE INHERITED NORMOTENSIVE HYPERKALEMIC ACIDOSIS. (June 2015) Authors: Picard, H. Louis Dit; Thurairajasingam, N.; Decramer, S.; Girerd, X.; Oshaugnessy, K.; Mulatero, P.; Roussey, G.; Tack, I.; Unwin, R.; Vargas-Poussou, R.; Jeunemaitre, X. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 43 THYROID FUNCTION AFFECTS BLOOD PRESSURE HOMEOSTASIS IN EUTHYROID HUMANS. (1st March 2004) Authors: Gumieniak, O.; Perlstein, T. S.; Hopkins, P.; Brown, N. J.; Jeunemaitre, X.; Williams, G. H. Journal: Journal of investigative medicine Issue: Volume 52(2004)Supplement 2 Page Start: S384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 49 INFLUENCE OF DIETARY SODIUM ON THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM AND PREVALENCE OF LEFT VENTRICULAR HYPERTROPHY BY EKG CRITERIA. (1st March 2004) Authors: Williams, J. S.; Williams, G. H.; Jeunemaitre, X.; Hopkins, P. N.; Conlin, P. R. Journal: Journal of investigative medicine Issue: Volume 52(2004)Supplement 2 Page Start: S385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 6C.01: CULLIN-3 MUTATIONS LEADING TO SKIPPING OF EXON 9 ARE RESPONSIBLE FOR SEVERE CASES OF FAMILIAL HYPERKALAEMIC HYPERTENSION. (June 2015) Authors: Picard, H. Louis Dit; Latreche, S.; Thurairajasingam, N.; Auzan, C.; Fiquet, B.; Frayssinet, R.; Garnier, A.; Jendruchova, V.; Lobbedez, T.; Martorell, L.; Mortier, G.; Pela, I.; Taque, S.; Vargas-Poussou, R.; Clauser, E.; Jeunemaitre, X. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA. (June 2015) Authors: Kiando, S.; Plouin, P.F.; Barlassina, M.C.; Cusi, D.; Galan, P.; Lathrop, M.; Jeunemaitre, X.; Bouatia-Naji, N. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 6D.03: FLOW-MEDIATED DILATATION (FMD) AND ENDOTHELIUM-INDEPENDENT DILATATION (EID) IN PATIENTS WITH MULTIFOCAL FIBROMUSCULAR DYSPLASIA. (June 2015) Authors: Khettab, H.; Lorthior, A.; Niarra, R.; Chambon, Y.; Jeunemaitre, X.; Plouin, P.F.; Laurent, S.; Boutouyrie, P.; Azizi, M. Journal: Journal of hypertension Issue: Volume 33(2015)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. [OP.1C.04] STRUCTURAL AND FUNCTIONAL ARTERIAL ABNORMALITIES IN FIBROMUSCULAR DYSPLASIA ARE IN THE CONTINUUM OF HYPERTENSION: AN IMAGING AND BIOMECHANICAL STUDY. (September 2016) Authors: Marais, L.; Boutouyrie, P.; Khettab, H.; Boulanger, C.; Lorthiroir, A.; Frank, M.; Niarra, R.; Renard, J.; Chambon, Y.; Jeunemaitre, X.; Zidi, M.; Plouin, P.-F.; Laurent, S.; Azizi, M. Journal: Journal of hypertension Issue: Volume 34:(2016) Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. [OP.7C.04] GENETIC ASSOCIATION STUDY IDENTIFIES COMMON VARIATION IN PHACTR1 TO ASSOCIATE WITH FIBROMUSCULAR DYSPLASIA. (September 2016) Authors: Kiando, S.; Tucker, N.; Castro-vega, L.; Cusi, D.; Galan, P.; J.-P., Empana; Olin, J.; Gornik, H.; Plouin, P.-F.; Kullo, I.; Milan, D.; Ganesh, S.; Boutouyrie, P.; Kovacic, J.; Jeunemaitre, X.; Bouatia-naji, N. Journal: Journal of hypertension Issue: Volume 34:(2016) Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. [OP.LB01.10] THE SKIPPING OF EXON 9 IN CULLIN-3 CAUSES A SEVERE FORM OF FAMILIAL HYPERKALEMIC HYPERTENSION IN MICE. (September 2016) Authors: Rafael, C.; Khalek, W. Abdel; Kouranti, I.; Clauser, E.; Jeunemaitre, X.; Hadchouel, J. Journal: Journal of hypertension Issue: Volume 34:(2016) Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. [OP.LB01.12] CACNA1H MUTATIONS ARE ASSOCIATED WITH YOUNG ONSET AND FAMILIAL FORMS OF PRIMARY ALDOSTERONISM. (September 2016) Authors: Daniil, G.; Fernandes-Rosa, F.L.; Chemin, J.; Jeunemaitre, X.; Polak, M.; Boulkroun, S.; Amar, L.; Strom, T.M.; Lory, P.; Zennaro, M.C. Journal: Journal of hypertension Issue: Volume 34:(2016) Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗