Cochat, Pierre

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Journal Article

Garrelfs, Sander F.; Frishberg, Yaacov; Hulton, Sally A.; Koren, Michael J.; O’Riordan, William D.; Cochat, Pierre; Deschênes, Georges; Shasha-Lavsky, Hadas; Saland, Jeffrey M.; van’t Hoff, William G.; Fuster, Daniel G.; Magen, Daniella; Moochhala, Shabbir H.; Schalk, Gesa; Simkova, Eva; Groothoff, Jaap W.; Sas, David J.; Meliambro, Kristin A.; Lu, Jiandong; Sweetser, Marianne T.; ... (2021). Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1. New England journal of medicine NEJM, 384(13), pp. 1216-1226. Massachusetts Medical Society MMS 10.1056/NEJMoa2021712

Allard, Lise; Cochat, Pierre; Leclerc, Anne-Laure; Cachat, François; Fichtner, Christine; De Souza, Vandréa Carla; Garcia, Clotilde Druck; Camoin-Schweitzer, Marie-Christine; Macher, Marie-Alice; Acquaviva-Bourdain, Cécile; Bacchetta, Justine (2015). Renal function can be impaired in children with primary hyperoxaluria type 3. Pediatric nephrology, 30(10), pp. 1807-1813. Springer 10.1007/s00467-015-3090-x

Mansour-Hendili, Lamisse; Blanchard, Anne; Le Pottier, Nelly; Roncelin, Isabelle; Lourdel, Stéphane; Treard, Cyrielle; González, Wendy; Vergara-Jaque, Ariela; Morin, Gilles; Colin, Estelle; Holder-Espinasse, Muriel; Bacchetta, Justine; Baudouin, Véronique; Benoit, Stéphane; Bérard, Etienne; Bourdat-Michel, Guylhène; Bouchireb, Karim; Burtey, Stéphane; Cailliez, Mathilde; Cardon, Gérard; ... (2015). Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1. Human mutation, 36(8), pp. 743-752. Wiley-Blackwell 10.1002/humu.22804

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