Centre Hospitalier Universitaire (CHU) de Toulouse

Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy (2022) Luppe J, Sticht H, Lecoquierre F, Goldenberg A, Gorman KM, Molloy B, Agolini E, et al. Journal article Clinical autonomic nervous system laboratories in Europe A joint survey of the European Academy of Neurology and the European Federation of Autonomic Societies (2022) Habek M, Leys F, Skoric MK, Carneiro DR, Calandra-Buonaura G, Camaradou J, Chiaro G, et al. Journal article The European Network of Autonomic Nervous System laboratories: an EAN-EFAS survey (2022) Habek M, Reis Carneiro D, Leys F, Buonaura GC, Camaradou J, Chiaro G, Cortelli P, et al. Conference contribution EAN-EFAS Survey on cardiovascular ANS disturbances following a SARS-CoV2 infection or COVID-19 vaccination (2022) Fanciulli A, Reis Carneiro D, Leys F, Buonaura GC, Camaradou J, Chiaro G, Cortelli P, et al. Conference contribution Multicomponent intervention to prevent mobility disability in frail older adults: randomised controlled trial (SPRINTT project) (2022) Bernabei R, Landi F, Calvani R, Cesari M, Del Signore S, Anker SD, Bejuit R, et al. Journal article LocoMMotion: a prospective, non-interventional, multinational study of real-life current standards of care in patients with relapsed and/or refractory multiple myeloma (2022) Mateos MV, Weisel K, De Stefano V, Goldschmidt H, Delforge M, Mohty M, Cavo M, et al. Journal article Definition and Diagnostic Criteria for Sarcopenic Obesity: ESPEN and EASO Consensus Statement (2022) Donini LM, Busetto L, Bischoff SC, Cederholm T, Ballesteros-Pomar MD, Batsis JA, Bauer JM, et al. Journal article Salvage total glossectomy and total glosso-laryngectomy: Are they worth it? A GETTEC French multicenter study. (2022) Mazerolle P, Fuchsmann C, Schultz P, Benmoussa N, Malard O, Bozec A, Deneuve S, et al. Journal article Definition and diagnostic criteria for sarcopenic obesity: ESPEN and EASO consensus statement. (2022) Donini LM, Busetto L, Bischoff SC, Cederholm T, Ballesteros-Pomar MD, Batsis JA, Bauer JM, et al. Journal article Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder (2022) Cuinat S, Nizon M, Isidor B, Stegmann A, van Jaarsveld RH, van Gassen KL, van der Smagt JJ, et al. Journal article