The variety of genetic defects explains the phenotypic heterogeneity of Familial Hyperkalemic Hypertension

por Hureaux, Marguerite, Mazurkiewicz, Stephani, Boccio, Valerie, Vargas-Poussou, Rosa, Jeunemaitre, Xavier
Publicado 2021

Pathophysiology of carotid-cavernous fistulas in vascular Ehlers-Danlos syndrome: a retrospective cohort and comprehensive review

por Adham, Salma, Trystram, Denis, Albuisson, Juliette, Domigo, Valérie, Legrand, Anne, Jeunemaitre, Xavier, Frank, Michael
Publicado 2018

Epigenetic control of vascular smooth muscle cells in Marfan and non-Marfan thoracic aortic aneurysms

por Gomez, Delphine, Coyet, Aurélie, Ollivier, Véronique, Jeunemaitre, Xavier, Jondeau, Guillaume, Michel, Jean-Baptiste, Vranckx, Roger
Publicado 2011

A New Methodology for Quantification of Alternatively Spliced Exons Reveals a Highly Tissue-Specific Expression Pattern of WNK1 Isoforms

por Vidal-Petiot, Emmanuelle, Cheval, Lydie, Faugeroux, Julie, Malard, Thierry, Doucet, Alain, Jeunemaitre, Xavier, Hadchouel, Juliette
Publicado 2012

Liddle Syndrome: Review of the Literature and Description of a New Case

por Tetti, Martina, Monticone, Silvia, Burrello, Jacopo, Matarazzo, Patrizia, Veglio, Franco, Pasini, Barbara, Jeunemaitre, Xavier, Mulatero, Paolo
Publicado 2018

Fibromuscular dysplasia

por Plouin, Pierre-François, Perdu, Jérôme, La Batide-Alanore, Agnès, Boutouyrie, Pierre, Gimenez-Roqueplo, Anne-Paule, Jeunemaitre, Xavier
Publicado 2007

Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse

por Perrocheau, Maëlle, Kiando, Soto Romuald, Vernerey, Déwi, Dina, Christian, Galan, Pilar, Hagege, Albert, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2015

Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling

por Kouranti, Ilektra, Abdel Khalek, Waed, Mazurkiewicz, Stephani, Loisel-Ferreira, Irmine, Gautreau, Alexis M., Pintard, Lionel, Jeunemaitre, Xavier, Clauser, Eric
Publicado 2022

POLYMORPHISMS IN THE SERUM- AND GLUCOCORTICOID-INDUCIBLE KINASE 1 GENE ARE ASSOCIATED WITH BLOOD PRESSURE AND RENIN RESPONSE TO DIETARY SALT INTAKE

por Rao, Ajay D, Sun, Bei, Saxena, Aditi, Hopkins, Paul N, Jeunemaitre, Xavier, Brown, Nancy J, Adler, Gail K, Williams, Jonathan S
Publicado 2012

A pseudo-dominant form of Gitelman’s syndrome

por de La Faille, Renaud, Vallet, Marion, Venisse, Annabelle, Nau, Valérie, Collet-Gaudillat, Carole, Houillier, Pascal, Jeunemaitre, Xavier, Vargas-Poussou, Rosa
Publicado 2011

The collαgen III fibril has a “flexi-rod” structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic roles

por Parkin, J. Des, San Antonio, James D., Persikov, Anton V., Dagher, Hayat, Dalgleish, Raymond, Jensen, Shane T., Jeunemaitre, Xavier, Savige, Judy
Publicado 2017

Carotid Stiffness Assessment With Ultrafast Ultrasound Imaging in Case of Bicuspid Aortic Valve

por Goudot, Guillaume, Mirault, Tristan, Khider, Lina, Pedreira, Olivier, Cheng, Charles, Porée, Jonathan, Gruest, Maxime, Jeunemaître, Xavier, Pernot, Mathieu, Messas, Emmanuel
Publicado 2019

Assessment of arterial damage in vascular Ehlers-Danlos syndrome: A retrospective multicentric cohort

por Adham, Salma, Legrand, Anne, Bruno, Rosa-Maria, Billon, Clarisse, Dalens, Violaine, Boutouyrie, Pierre, Mazzella, Jean-Michaël, Gueguen, Sonia, Frank, Michael, Mirault, Tristan, Jeunemaitre, Xavier
Publicado 2022

Oral phenotype and scoring of vascular Ehlers–Danlos syndrome: a case–control study

por Ferré, François Côme, Frank, Michael, Gogly, Bruno, Golmard, Lisa, Naveau, Adrien, Chérifi, Hafida, Emmerich, Joseph, Gaultier, Frédérick, Berdal, Ariane, Jeunemaitre, Xavier, Fournier, Benjamin P J
Publicado 2012

Comparative therapeutic strategies for preventing aortic rupture in a mouse model of vascular Ehlers-Danlos syndrome

por Legrand, Anne, Guery, Charline, Faugeroux, Julie, Fontaine, Erika, Beugnon, Carole, Gianfermi, Amélie, Loisel-Ferreira, Irmine, Verpont, Marie-Christine, Adham, Salma, Mirault, Tristan, Hadchouel, Juliette, Jeunemaitre, Xavier
Publicado 2022

CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism

por Daniil, Georgios, Fernandes-Rosa, Fabio L, Chemin, Jean, Blesneac, Iulia, Beltrand, Jacques, Polak, Michel, Jeunemaitre, Xavier, Boulkroun, Sheerazed, Amar, Laurence, Strom, Tim M, Lory, Philippe, Zennaro, Maria-Christina
Publicado 2016

A severe case of PLOD1 ‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report

por Foy, Malika, Métay, Corinne, Frank, Michael, Denarié, Nicolas, Adham, Salma, Billon, Clarisse, Legrand, Anne, Jeunemaitre, Xavier, Gillas, Fabrice, Gaudon, Karen, De Mazancourt, Philippe, Mekki, Ahmed, Carlier, Robert, Benistan, Karelle
Publicado 2023

Interplay Between Statins, Cav1 (Caveolin-1), and Aldosterone

por Haas, Andrea V., Baudrand, Rene, Easly, Rebecca M., Murray, Gillian R., Touyz, Rhian M., Pojoga, Luminita H., Jeunemaitre, Xavier, Hopkins, Paul N., Rosner, Bernard, Williams, Jonathan S., Williams, Gordon H., Adler, Gail K.
Publicado 2020

Caveolin 1 Modulates Aldosterone‐Mediated Pathways of Glucose and Lipid Homeostasis

por Baudrand, Rene, Gupta, Nidhi, Garza, Amanda E., Vaidya, Anand, Leopold, Jane A., Hopkins, Paul N., Jeunemaitre, Xavier, Ferri, Claudio, Romero, Jose R., Williams, Jonathan, Loscalzo, Joseph, Adler, Gail K., Williams, Gordon H., Pojoga, Luminita H.
Publicado 2016

Male Sex Is Associated With Cervical Artery Dissection in Patients With Fibromuscular Dysplasia

por Arnaud, Charlotte, Boulanger, Marion, Lorthioir, Aurélien, Amar, Laurence, Azarine, Arshid, Boyer, Louis, Chatellier, Gilles, Di Monaco, Silvia, Jeunemaitre, Xavier, Kastler, Adrian, Mousseaux, Elie, Oppenheim, Catherine, Thony, Frédéric, Persu, Alexandre, Olin, Jeffrey W., Azizi, Michel, Touzé, Emmanuel
Publicado 2021