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Muscle & Nerve|February 21, 2013
Sensory chronic inflammatory demyelinating polyneuropathy: an under-recognized entity?Xavier Ayrignac, Karine Viala, Régine Morizot Koutlidis, et al.Journal of the Peripheral Nervous System : JPNS|April 3, 2012
Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4CMarion Yger, Tanya Stojkovic, Sandrine Tardieu, et al.Respiratory Medicine and Research|June 11, 2026
Determinants of diaphragm ultrasound and its diagnostic performance for predicting respiratory status in myotonic dystrophy type 1Abdallah Fayssoil, Marie De Antonio, Helene Prigent, et al.Muscle & Nerve|January 20, 2018
The role of electrodiagnosis with long exercise test in mcardle diseaseClaudio Semplicini, Marianne Hézode-Arzel, Pascal Laforêt, et al.Journal of the Peripheral Nervous System : JPNS|June 22, 2006
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutationsPhilippe Latour, Pierre-Marie Gonnaud, Elisabeth Ollagnon, et al.Muscle & Nerve|August 12, 2009
Permanent muscle weakness in McArdle diseaseAleksandra A Nadaj-Pakleza, Carlo M Vincitorio, Pascal Laforêt, et al.Journal of Neuromuscular Diseases|February 25, 2026
Congenital core myopathy linked to SOX5: Expanding the phenotypical spectrum of Lamb-Shaffer syndromeKatia Staedler, Anna Gerasimenko, Caroline Nava, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 2, 2017
Two-dimensional electrophoresis highlights haptoglobin beta chain as an additional biomarker of congenital disorders of glycosylationArnaud Bruneel, Florence Habarou, Tanya Stojkovic, et al.European Journal of Neurology|March 31, 2025
Disease Trajectories of a Large French Cohort of 142 Congenital Myopathy Patients in Adult AgeMichela Bisciglia, Gianmarco Severa, Norma Beatriz Romero, et al.Medicine|September 3, 2004
Neurologic manifestations in primary Sjögren syndrome: a study of 82 patientsSophie Delalande, Jérôme de Seze, Anne-Laure Fauchais, et al.Pageof 25