France (FR)

LHX2 haploinsufficiency causes a variable neurodevelopmental disorder (2023) Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, et al. Journal article M cell maturation and cDC activation determine the onset of adaptive immune priming in the neonatal Peyer's patch (2023) Torow N, Li R, Hitch TCA, Mingels C, Al Bounny S, van Best N, Stange EL, et al. Journal article Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy (2023) Khoshkhoo S, Wang Y, Chahine Y, Erson-Omay EZ, Robert SM, Kiziltug E, Damisah EC, et al. Journal article Using continuous electrical conductivity measurements to derive major solute concentrations in karst systems (2023) Richieri B, Bittner D, Hartmann A, Benettin P, van Breukelen BM, Labat D, Chiogna G Journal article Effect of the COVID-19 pandemic on surgery for indeterminate thyroid nodules (THYCOVID): a retrospective, international, multicentre, cross-sectional study (2023) Medas F, Dobrinja C, Al-Suhaimi EA, Altmeier J, Anajar S, Arikan AE, Azaryan I, et al. Journal article Splitting probabilities for dynamics in corrugated channels: Passive vs. active Brownian motion (a) (2023) Malgaretti P, Nizkaia T, Oshanin G Journal article Standardization of the Definition and Surgical Management of Splenic Flexure Carcinoma by an International Expert Consensus Using the Delphi Technique: Room for Improvement? (2023) Benlice C, Parvaiz A, Baca B, Hohenberger W, Miskovic D, Stocchi L, Steele S, et al. Journal article Impact of the COVID-19 pandemic on clinical autonomic practice in Europe: a survey of the European Academy of Neurology and the European Federation of Autonomic Societies (2023) Fanciulli A, Leys F, Krbot Skorić M, Reis Carneiro D, Calandra-Buonaura G, Camaradou J, Chiaro G, et al. Journal article Competition and moral behavior: A meta-analysis of forty-five crowd-sourced experimental designs (2023) Huber C, Dreber A, Huber J, Johannesson M, Kirchler M, Weitzel U, Abellán M, et al. Journal article Germline C1GALT1C1 mutation causes a multisystem chaperonopathy (2023) Erger F, Aryal RP, Reusch B, Matsumoto Y, Meyer R, Zeng J, Knopp C, et al. Journal article