Results 321 to 330 of about 183,642 (350)
Some of the next articles are maybe not open access.
Continuum, 2013
This article reviews the most important muscle toxins, many of which are widely prescribed medications. Particular emphasis is placed on statins, which cause muscle symptoms in a relatively large proportion of the patients who take them.As with other toxic myopathies, most cases of statin-associated myotoxicity are self-limited and subside with ...
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This article reviews the most important muscle toxins, many of which are widely prescribed medications. Particular emphasis is placed on statins, which cause muscle symptoms in a relatively large proportion of the patients who take them.As with other toxic myopathies, most cases of statin-associated myotoxicity are self-limited and subside with ...
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Current Opinion in Neurology, 1996
As well as myositis caused by infectious agents, there is a spectrum of inflammatory myopathies representing diseases with autoimmune response. Subtypes differing in clinical features and morphological characteristics have been described. This review will emphasize new advances and recent efforts to identify pathogenetic mechanisms and immunological ...
D S, Tews, H H, Goebel
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As well as myositis caused by infectious agents, there is a spectrum of inflammatory myopathies representing diseases with autoimmune response. Subtypes differing in clinical features and morphological characteristics have been described. This review will emphasize new advances and recent efforts to identify pathogenetic mechanisms and immunological ...
D S, Tews, H H, Goebel
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2013
Congenital myopathies are a heterogeneous group of inherited muscle disorders, characterized by the predominance of particular histopathological features on muscle biopsy, such as cores (central core disease) or rods (nemaline myopathy). Clinically, early onset of the disease, stable or slowly progressive muscle weakness, hypotonia and delayed motor ...
Norma Beatriz, Romero, Nigel F, Clarke
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Congenital myopathies are a heterogeneous group of inherited muscle disorders, characterized by the predominance of particular histopathological features on muscle biopsy, such as cores (central core disease) or rods (nemaline myopathy). Clinically, early onset of the disease, stable or slowly progressive muscle weakness, hypotonia and delayed motor ...
Norma Beatriz, Romero, Nigel F, Clarke
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Current Opinion in Neurology, 2010
This review summarizes the recent progress in understanding of myopathies induced by therapeutic agents, the underlying pathogenetic mechanisms and the management of iatrogenic muscle disorders, focussing on statin-associated myopathies.Recent reports from observational studies have provided further information on the frequency of statin-associated ...
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This review summarizes the recent progress in understanding of myopathies induced by therapeutic agents, the underlying pathogenetic mechanisms and the management of iatrogenic muscle disorders, focussing on statin-associated myopathies.Recent reports from observational studies have provided further information on the frequency of statin-associated ...
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2011
Myofibrillar myopathies (MFMs) represent a group of muscular dystrophies with a similar morphological phenotype. The diagnosis is established by muscle biopsy. The MFMs are characterized by a distinct pathological pattern of myofibrillar dissolution associated with disintegration of the Z-disk, accumulation of myofibrillar degradation products, and ...
Duygu, Selcen, Andrew G, Engel
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Myofibrillar myopathies (MFMs) represent a group of muscular dystrophies with a similar morphological phenotype. The diagnosis is established by muscle biopsy. The MFMs are characterized by a distinct pathological pattern of myofibrillar dissolution associated with disintegration of the Z-disk, accumulation of myofibrillar degradation products, and ...
Duygu, Selcen, Andrew G, Engel
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Immune-mediated necrotizing myopathy: clinical features and pathogenesis
Nature Reviews Rheumatology, 2020Yves Allenbach +2 more
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