Items where Author is "Azizi, Michel"

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Persu, Alexandre and Dobrowolski, Piotr and Gornik, Heather L and Olin, Jeffrey W and Adlam, David and Azizi, Michel and Boutouyrie, Pierre and Bruno, Rosa Maria and Boulanger, Marion and Demoulin, Jean-Baptiste and Ganesh, Santhi K and J. Guzik, Tomasz and Januszewicz, Magdalena and Kovacic, Jason C and Kruk, Mariusz and de Leeuw, Peter and Loeys, Bart L and Pappaccogli, Marco and Perik, Melanie H A M and Touzé, Emmanuel and Van der Niepen, Patricia and Van Twist, Daan J L and Warchoł-Celińska, Ewa and Prejbisz, Aleksander and Januszewicz, Andrzej (2022) Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia. Cardiovascular Research, 118 (1). pp.65-83. ISSN 0008-6363

Georges, Adrien and Yang, Min-Lee and Berrandou, Takiy-Eddine and Bakker, Mark K. and Dikilitas, Ozan and Kiando, Soto Romuald and Ma, Lijiang and Satterfield, Benjamin A. and Sengupta, Sebanti and Yu, Mengyao and Deleuze, Jean-François and Dupré, Delia and Hunker, Kristina L. and Kyryachenko, Sergiy and Liu, Lu and Sayoud-Sadeg, Ines and Amar, Laurence and Brummett, Chad M. and Coleman, Dawn M. and d’Escamard, Valentina and de Leeuw, Peter and Fendrikova-Mahlay, Natalia and Kadian-Dodov, Daniella and Li, Jun Z. and Lorthioir, Aurélien and Pappaccogli, Marco and Prejbisz, Aleksander and Smigielski, Witold and Stanley, James C. and Zawistowski, Matthew and Zhou, Xiang and Zöllner, Sebastian and de Leeuw, Peter and Amouyel, Philippe and De Buyzere, Marc L. and Debette, Stéphanie and Dobrowolski, Piotr and Drygas, Wojciech and Gornik, Heather L. and Olin, Jeffrey W. and Piwonski, Jerzy and Rietzschel, Ernst R. and Ruigrok, Ynte M. and Vikkula, Miikka and Warchol Celinska, Ewa and Januszewicz, Andrzej and Kullo, Iftikhar J. and Azizi, Michel and Jeunemaitre, Xavier and Persu, Alexandre and Kovacic, Jason C. and Ganesh, Santhi K. and Bouatia-Naji, Nabila (2021) Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications, 12 (1). ISSN 2041-1723

Georges, Adrien and Albuisson, Juliette and Berrandou, Takiy and Dupré, Délia and Lorthioir, Aurélien and D’Escamard, Valentina and Di Narzo, Antonio F and Kadian-Dodov, Daniella and Olin, Jeffrey W and Warchol-Celinska, Ewa and Prejbisz, Aleksander and Januszewicz, Andrzej and Bruneval, Patrick and Baranowska, Anna A and Webb, Tom R and Hamby, Stephen E and Samani, Nilesh J and Adlam, David and Fendrikova-Mahlay, Natalia and Hazen, Stanley and Wang, Yu and Yang, Min-Lee and Hunker, Kristina and Combaret, Nicolas and Motreff, Pascal and Chédid, Antoine and Fiquet, Béatrice and Plouin, Pierre-François and Mousseaux, Elie and Azarine, Arshid and Amar, Laurence and Azizi, Michel and Gornik, Heather L and Ganesh, Santhi K and Kovacic, Jason C and Jeunemaitre, Xavier and Bouatia-Naji, Nabila (2021) Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia. Cardiovascular Research, 117 (4). pp.1154-1165. ISSN 0008-6363

This list was generated on Tue Aug 9 12:23:35 2022 AEST.