Works matching IS 11282460 AND DT 2020 AND VI 39 AND IP 4
Results: 22
Spinal cord injuries, human neuropathology and neurophysiology.
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- Acta Myologica, 2020, v. 39, n. 4, p. 353, doi. 10.36185/2532-1900-039
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Myasthenia gravis: MuSK MG, late-onset MG and ocular MG.
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- Acta Myologica, 2020, v. 39, n. 4, p. 345, doi. 10.36185/2532-1900-038
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25 years of the SMN genes: the Copernican revolution of spinal muscular atrophy.
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- Acta Myologica, 2020, v. 39, n. 4, p. 336, doi. 10.36185/2532-1900-037
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Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome.
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- Acta Myologica, 2020, v. 39, n. 4, p. 320, doi. 10.36185/2532-1900-036
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The correlation between cardiac and skeletal muscle pathology in animal models of idiopathic inflammatory myopathies.
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- Acta Myologica, 2020, v. 39, n. 4, p. 313, doi. 10.36185/2532-1900-035
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The impact of SARS-CoV-2 on skeletal muscles.
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- Acta Myologica, 2020, v. 39, n. 4, p. 307, doi. 10.36185/2532-1900-034
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Giant cell myositis and myocarditis revisited.
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- Acta Myologica, 2020, v. 39, n. 4, p. 302, doi. 10.36185/2532-1900-033
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Inflammatory myopathies: update on diagnosis, pathogenesis and therapies, and COVID-19-related implications.
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- Acta Myologica, 2020, v. 39, n. 4, p. 289, doi. 10.36185/2532-1900-032
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The changing spectrum of drug-induced myopathies.
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- Acta Myologica, 2020, v. 39, n. 4, p. 283, doi. 10.36185/2532-1900-031
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Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients.
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- Acta Myologica, 2020, v. 39, n. 4, p. 274, doi. 10.36185/2532-1900-030
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Core myopathies - a short review.
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- Acta Myologica, 2020, v. 39, n. 4, p. 266, doi. 10.36185/2532-1900-029
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Panorama of the distal myopathies.
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- Acta Myologica, 2020, v. 39, n. 4, p. 245, doi. 10.36185/2532-1900-028
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Late-onset myopathies: clinical features and diagnosis.
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- Acta Myologica, 2020, v. 39, n. 4, p. 235, doi. 10.36185/2532-1900-027
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Myotonic dystrophy type 2: the 2020 update.
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- Acta Myologica, 2020, v. 39, n. 4, p. 222, doi. 10.36185/2532-1900-026
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Alpha-sarcoglycanopathy presenting as myalgia and hyperCKemia in two adults with a long-term follow-up. Case reports.
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- Acta Myologica, 2020, v. 39, n. 4, p. 218, doi. 10.36185/2532-1900-025
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LGMD. Identification, description and classification.
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- Acta Myologica, 2020, v. 39, n. 4, p. 207, doi. 10.36185/2532-1900-024
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Quadriceps muscle strength in Duchenne muscular dystrophy and effect of corticosteroid treatment.
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- Acta Myologica, 2020, v. 39, n. 4, p. 200, doi. 10.36185/2532-1900-023
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Giovanni Nigro and the Naples's school: historical contribution to the knowledge of heart involvement in Duchenne/Becker muscular dystrophies.
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- Acta Myologica, 2020, v. 39, n. 4, p. 187, doi. 10.36185/2532-1900-021
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Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies.
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- Acta Myologica, 2020, v. 39, n. 4, p. 179, doi. 10.36185/2532-1900-020
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Giovanni Nigro A note of remembrance.
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- Acta Myologica, 2020, v. 39, n. 4, p. 177
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25<sup>th</sup> Anniversary of the Founding of the World Muscle Society (1995-2020). The Contribution of Prof. Giovanni Nigro (1931-2017).
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- Acta Myologica, 2020, v. 39, n. 4, p. 174
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Impaired myocardial strain in early stage of Duchenne muscular dystrophy: its relation with age and motor performance.
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- Acta Myologica, 2020, v. 39, n. 4, p. 191, doi. 10.36185/2532-1900-022
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