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Vox Sanguinis|December 13, 2021
COVID-19 convalescent plasma: Evolving strategies for serological screening in FrancePierre Gallian, Sophie Le Cam, Nadège Brisbarre, et al.
Vox Sanguinis|May 15, 2023
Evolving deferral criteria for blood donation in France: Plasma donation by men who have sex with menPierre Tiberghien, Sophie Lecam, Julie Huet, et al.
Blood Transfusion = Trasfusione Del Sangue|August 15, 2022
Seven years (2015-2021) of blood donor screening for HEV-RNA in France: lessons and perspectivesSyria Laperche, Claude Maugard, Sébastien Lhomme, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
EMBO Reports|February 25, 2006
A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathyValérie Allamand, Pascale Richard, Alain Lescure, et al.
Viruses|November 24, 2022
Insights on 21 Years of HBV Surveillance in Blood Donors in FrancePierre Cappy, Laure Boizeau, Daniel Candotti, et al.
Plos One|August 3, 2017
Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasiaJoel Fedida, Veronique Fressart, Philippe Charron, et al.
Frontiers in Aging Neuroscience|September 6, 2014
Aggresome-Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 GenePatrizia Sabatelli, Silvia Castagnaro, Francesca Tagliavini, et al.
Iscience|February 23, 2023
SARS-CoV-2 IgG seroprevalence surveys in blood donors before the vaccination campaign, France 2020-2021Pierre Gallian, Nathanaël Hozé, Nadège Brisbarre, et al.
Neuromuscular Disorders : NMD|December 9, 2003
Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutationEriko Yasaki, Cassandra Prioleau, Julien Barbier, et al.
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