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European Journal of Neurology|October 2, 2025
Camptocormia as a Phenotypic Variant of FSHD in the Elderly: Clinical, Genetic, and Imaging FeaturesEleonora Torchia, Patrick Vandeputte, Mauro Monforte, et al.Acta Neuropathologica Communications|October 18, 2023
Muscle fibrosis as a prognostic biomarker in facioscapulohumeral muscular dystrophy: a retrospective cohort studyElvira Ragozzino, Sara Bortolani, Lorena Di Pietro, et al.Cerebellum (London, England)|February 25, 2018
Novel Homozygous KCNJ10 Mutation in a Patient with Non-syndromic Early-Onset Cerebellar AtaxiaFrancesco Nicita, Giorgio Tasca, Marta Nardella, et al.Practical Neurology|July 1, 2026
Oculopharyngeal muscular dystrophy: diagnosis, management and multisystem careWesley Reintjes, Simone Knuijt, Fien Oelbrandt, et al.Frontiers in Psychology|April 18, 2022
Examining Shared Pathways for Eating Disorders and Obesity in a Community Sample of Adolescents: The REAL StudyNicole Obeid, Martine F Flament, Annick Buchholz, et al.Journal of Neurology|January 23, 2018
Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohortMauro Monforte, Guido Primiano, Gabriella Silvestri, et al.BMC Pulmonary Medicine|May 22, 2020
Correction to: Assessment of stigma in patients with cystic fibrosisSmita Pakhale, Michael Armstrong, Crystal Holly, et al.Neuromuscular Disorders : NMD|April 24, 2012
New phenotype and pathology features in MYH7-related distal myopathyGiorgio Tasca, Enzo Ricci, Sini Penttilä, et al.European Journal of Neurology|December 28, 2021
Technology outcome measures in neuromuscular disorders: A systematic reviewSara Bortolani, Chiara Brusa, Enrica Rolle, et al.BMC Pulmonary Medicine|June 3, 2014
Assessment of stigma in patients with cystic fibrosisSmita Pakhale, Michael Armstrong, Crystal Holly, et al.Pageof 16