Filter Filter By date Start date End date By Team Michel Polak Alessandra Pierani Patrick Revy & Erika Brunet Sigolène Meilhac Laurent Abel Jeanne Amiel et Laurence Legeai‑Mallet Antonio Rausell Isabelle André Vincent Cantagrel Jean-Laurent Casanova Nadine Cerf-Bensussan Yanick Crow Olivier Hermine & Thiago Trovati Maciel Alain Hovnanian Edor Kabashi Sylvain Latour Valérie Cormier-Daire Mickaël Ménager Gaël Ménasché et Fernando Sepulveda Annarita Miccio Frédéric Rieux-Laucat Agnès Rötig Jean-Michel Rozet Sophie Saunier et Corinne Antignac Matias Simons Nathalie Boddaert Sabine Sarnacki et Isabelle Bloch Yves Ville Anne DUMAINE Patrick Nitschké Corinne Cordier Meriem Garfa-Traoré Sylvie Fabrega Marie-Alexandra Alyanakian Sophie Berissi Chiara Guerrera Pierre David Nathalie Lefort Claude Besmond Marcelo Simon Sola LEAT Nathalie Boddaert Travail en collaboration : Unité de Recherche clinique-Centre d’investigation clinique (URC-CIC) Travail en collaboration : Département de Biothérapie, Centre d'Investigation Clinique pour les Thérapies Innovantes Salma Kotti Nicolas Garcelon Mickaël Ménager Michela Deleidi Annarita Miccio Annarita Miccio Jean Michel Rozet Sara Bizzotto Elodie Bal Bana Jabri Hossein Khonsari Karim Wahbi Lucile Couronné Denis Jabaudon, Thomas Blauwblomme et Rima Nabbout Bana Jabri Céline GRECO Filter Reset 0 results match your search. Publications Renal Atp6ap2/(Pro)renin Receptor Is Required for Normal Vacuolar H+-ATPase... Publications In utero treatment of congenital cytomegalovirus infection with valacyclovir... Publications A genome wide association study identifies a lncRna as risk factor for... Publications Reticular dysgenesis: international survey on clinical presentation, transplantation,... Publications APOL1-Mediated Cell Injury Involves Disruption of Conserved Trafficking... Publications Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe... Publications Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness... Publications Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrom... Publications Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing... Publications Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Ne... Publications Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Inf... Publications Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Inf... Publications Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause... Publications Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause... Publications Improving a full-text search engine: the importance of negation detection... Pagination First page Previous Page … Page 36 Page 37 Page 38 Page 39 Current page 40 Page 41 Page 42 Page 43 Page 44 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
