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 Evolution of disease activity and biomarkers on and off rapamycin in 28... Publications Basal exon skipping and nonsense-associated altered splicing allows bypassing... Publications Basal exon skipping and nonsense-associated altered splicing allows bypassing... Publications Epithelial barrier dysfunction in desmoglein-1 deficiency. Publications Basal exon skipping and nonsense-associated altered splicing allows bypassing... Publications Cortical developmental death: selected to survive or fated to die. Publications Hemophagocytic syndrome: primary forms and predisposing conditions. Publications What's up in the ALPS. Publications Whole-genome sequencing in patients with ciliopathies uncovers a novel... Publications Loss of function IFT27 variants associated with an unclassified lethal... Publications A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency... Publications Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli... Publications Enhanced Abventricular Proliferation Compensates Cell Death in the Embryonic... Publications Next Generation Phenotyping Using Narrative Reports in a Rare Disease Clinical... Publications A human patient-derived cellular model of Joubert syndrome reveals ciliary... Pagination First page Previous Page … Page 30 Page 31 Page 32 Page 33 Current page 34 Page 35 Page 36 Page 37 Page 38 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
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