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Orphanet Journal of Rare Diseases|March 3, 2022
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral DystrophyBenoît Sanson, Caroline Stalens, Céline Guien, et al.
Revue Neurologique|April 5, 2023
Current clinical management of CIDP with immunoglobulins in France: An expert opinionP Cintas, F Bouhour, C Cauquil, et al.
Heart Rhythm|July 13, 2014
Prevalence of type 1 Brugada ECG pattern after administration of Class 1C drugs in patients with type 1 myotonic dystrophy: Myotonic dystrophy as a part of the Brugada syndromePhilippe Maury, Mathieu Audoubert, Pascal Cintas, et al.
Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.
Molecular Cancer Therapeutics|September 23, 2021
Phosphoproteomics Identifies PI3K Inhibitor-selective Adaptive Responses in Pancreatic Cancer Cell Therapy and ResistanceCélia Cintas, Thibault Douche, Zahra Dantes, et al.
Journal of Fungi (Basel, Switzerland)|January 22, 2021
Utility of 1,3 β-d-Glucan Assay for Guidance in Antifungal Stewardship Programs for Oncologic Patients and Solid Organ Transplant RecipientsMarina Machado, Esther Chamorro de Vega, María Del Carmen Martínez-Jiménez, et al.
Journal of Neuromuscular Diseases|July 8, 2025
REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in FranceLamiae Grimaldi, Rocio Garcia-Uzquiano, Marta Gomez-Garcia de la Banda, et al.
European Journal of Neurology|November 1, 2008
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective studyJ Gil, B Funalot, A Verschueren, et al.
Neuromuscular Disorders : NMD|March 7, 2023
A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapyR Barrois, C Barnerias, E Deladrière, et al.
Journal of Inherited Metabolic Disease|January 8, 2026
MRPS Genes Causing Leukoencephalopathy With Profound Cerebral Folate Deficiency in AdultsDaniele Mandia, Metodi D Metodiev, Jean-François Benoist, et al.
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