Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gaelle Rey"'
Autor:
Eléonore Kaphan, François Bettega, Edouard Forcade, Hélène Labussière-Wallet, Nathalie Fegueux, Marie Robin, Régis Peffault De Latour, Anne Huynh, Léopoldine Lapierre, Ana Berceanu, Ambroise Marcais, Pierre-Edouard Debureaux, Nicolas Vanlangendonck, Claude-Eric Bulabois, Leonardo Magro, Adrien Daniel, Jean Galtier, Bruno Lioure, Patrice Chevallier, Chloé Antier, Michael Loschi, Gaelle Guillerm, Jean-Baptiste Mear, Sylvain Chantepie, Jérome Cornillon, Gaelle Rey, Xavier Poire, Ali Bazarbachi, Marie-Thérèse Rubio, Nathalie Contentin, Corentin Orvain, Rémy Dulery, Jacques Olivier Bay, Carolyne Croizier, Yves Beguin, Aude Charbonnier, Caroline Skrzypczak, Déborah Desmier, Alban Villate, Martin Carré, Anne Thiebaut-Bertrand
Publikováno v:
Transplantation and Cellular Therapy. 29:362.e1-362.e12
Autor:
Alexandre Janin, Thomas Perouse de Montclos, Karine Nguyen, Emilie Consolino, Gwenael Nadeau, Gaelle Rey, Océane Bouchot, Patricia Blanchet, Quentin Sabbagh, Cécile Cazeneuve, Rajae El-Malti, Elodie Morel, Antoine Delinière, Philippe Chevalier, Gilles Millat
Publikováno v:
Molecular diagnosistherapy. 26(5)
Pediatric cardiomyopathies are clinically heterogeneous heart muscle disorders associated with significant morbidity and mortality for which substantial evidence for a genetic contribution was previously reported. We present a detailed molecular inve
Autor:
Andreea Apetrei, Arnaud Molin, Nicolas Gruchy, Manon Godin, Claire Bracquemart, Antoine Resbeut, Gaëlle Rey, Gwenaël Nadeau, Nicolas Richard
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 101073- (2021)
Introduction: Pseudohypoparathyroidism type 1A (PHP1A) and pseudopseudohypoparathyroidism (PPHP) (Inactivating PTH/PTHrP Signaling Disorders type 2, IPPSD2) are two rare autosomal disorders caused by loss-of-function mutations on either maternal or p
Externí odkaz:
https://doaj.org/article/06afffac08b845edbeaae027d8bd8669