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M Mode Ultrasound and Tissue Doppler Imaging to Assess Diaphragm Feature in Late Onset Pompe Disease
Meng P, Ogna A, Fayssoil A
Neurology International, 2020, 12, 3, p 55
Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine
Durmus H, Sticht H, Ceylaner S, et al.
Acta neurologica Belgica, 2020
Electrodiagnostic accuracy in polyneuropathies: supervised learning algorithms as a tool for practitioners
Uncini A, Aretusi G, Manganelli F, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Pediatric anti-HMGCR necrotizing myopathy: diagnostic challenges and literature review
Velardo D, Faravelli I, Cinnante C, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Social, professional and neuropsychiatric outcomes in patients with myasthenia gravis
Vitturi BK, Kim AIH, Mitre LP, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A
Bjelica B, Peric S, Bozovic I, et al.
Acta neurologica Belgica, 2020
Ventral tegmental area dysfunction affects decision-making in patients with myotonic dystrophy type-1
Serra L, Scocchia M, Meola G, et al.
Cortex; a journal devoted to the study of the nervous system and behavior, 2020, 128, p 192
Anoctamin 5 (ANO5) muscular dystrophy-three different phenotypes and a new histological pattern
Segui F, Gonzalez-Quereda L, Sanchez A, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Psychosocial impact of sport activity in neuromuscular disorders
Vita GL, Stancanelli C, La Foresta S, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Recognition of emotions conveyed by facial expression and body postures in myotonic dystrophy (DM)
Lenzoni S, Bozzoni V, Burgio F, et al.
Cortex; a journal devoted to the study of the nervous system and behavior, 2020, 127, p 58
Neuromuscular diseases rehabilitation in the era of gene therapy
Trabacca A
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
One year in review 2019: idiopathic inflammatory myopathies
Tripoli A, Marasco E, Cometi L, et al.
Clinical and experimental rheumatology, 2020, 38, 1, p 1
Accumulation of autophagosome cargo protein p62 is common in idiopathic inflammatory myopathies
Milisenda JC, Pinal-Fernández I, Lloyd TE, et al.
Clinical and experimental rheumatology, 2020
The International Classification of Functioning, Disability and Health-Children and Youth as a framework for the management of spinal muscular atrophy in the era of gene therapy: a proof-of-concept study
Trabacca A, Lucarelli E, Pacifico R, et al.
European journal of physical and rehabilitation medicine, 2020
Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center
Gentile L, Russo M, Fabrizi GM, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
A novel missense pathogenic variant in NEFH causing rare Charcot-Marie-Tooth neuropathy type 2CC
Yan J, Qiao L, Peng H, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2020
Exercise in neuromuscular disorders: a promising intervention
Voet NBM
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019, 38, 4, p 207
Exercise therapy for muscle and lower motor neuron diseases
Sheikh AM, Vissing J
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019, 38, 4, p 215
Exercise therapy in muscle diseases: open issues and future perspectives
Siciliano G, Schirinzi E, Simoncini C, et al.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019, 38, 4, p 233
Fatigue in myotonic dystrophy type 1: a seven-year prospective study
Peric S, Bjelica B, Bozovic I, et al.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019, 38, 4, p 239
Physiological aspects of muscular adaptations to training translated to neuromuscular diseases
Berardinelli A, D'Antona G
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019, 38, 4, p 197
Late-onset generalized myasthenia gravis: clinical features, treatment, and outcome
Yildiz Celik S, Durmus H, Yilmaz V, et al.
Acta neurologica Belgica, 2019
Treatment of calcinosis associated with adult and juvenile dermatomyositis using topical sodium thiosulfate via fractionated CO2 laser treatment
Eleryan MG, Awosika O, Akhiyat S, et al.
Clinical and experimental rheumatology, 2019, 37, 6, p 1092
Thrombocytopenia in idiopathic inflammatory myopathies: a case series analysis
Giannini M, Grignaschi S, Fornaro M, et al.
Clinical and experimental rheumatology, 2019
Adapted physical activity and therapeutic exercise in late-onset Pompe disease (LOPD): a two-step rehabilitative approach
Iolascon G, Vitacca M, Carraro E, et al.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019
