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La Revue Du Praticien|January 23, 2009
[Dysimmune neuropathies: current diagnosis and therapy]Jean-Marc Léger, Sandrine Larue, Florian DashiBMC Musculoskeletal Disorders|November 22, 2014
Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) presenting as diffuse myositisMarc-Etienne Parent, Sandrine Larue, Benjamin EllezamThe Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 2, 2006
A case of familial Creutzfeldt-Jakob disease presenting with dry coughSandrine Larue, Steve Verreault, Peter Gould, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Distal muscle involvement in granulomatous myositis can mimic inclusion body myositisSandrine Larue, Thierry Maisonobe, Olivier Benveniste, et al.Neurology. Genetics|April 28, 2020
Molecular diagnosis of muscular diseases in outpatient clinics: A Canadian perspectiveFanny Thuriot, Elaine Gravel, Caroline Buote, et al.Orphanet Journal of Rare Diseases|January 27, 2016
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencingSébastien Lévesque, Christiane Auray-Blais, Elaine Gravel, et al.Neuromuscular Disorders : NMD|January 17, 2023
Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositisAlain Meyer, Yves Troyanov, Pat Korathanakhun, et al.Arthritis Research & Therapy|January 10, 2020
Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patientsAlain Meyer, Yves Troyanov, Julie Drouin, et al.Pageof 1