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Hereditary neuromuscular diseases
European Journal of Radiology, 2001This article presents the actual classification of neuromuscular diseases based on present expansion of our knowledge and understanding due to genetic developments. It summarizes the genetic and clinical presentations of each disorder together with CT findings, which we studied in a large group of patients with neuromuscular diseases.
Özsarlak, Ö. +6 more
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Seminars in Neurology, 2009
Neuromuscular diseases are a broadly defined group of disorders that all involve injury or dysfunction of peripheral nerves or muscle. The site of injury can be in the cell bodies (i.e., amyotrophic lateral sclerosis [ALS] or sensory ganglionopathies), axons (i.e., axonal peripheral neuropathies or brachial plexopathies), Schwann cells (i.e., chronic ...
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Neuromuscular diseases are a broadly defined group of disorders that all involve injury or dysfunction of peripheral nerves or muscle. The site of injury can be in the cell bodies (i.e., amyotrophic lateral sclerosis [ALS] or sensory ganglionopathies), axons (i.e., axonal peripheral neuropathies or brachial plexopathies), Schwann cells (i.e., chronic ...
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2016
Abstract Types of myopathy, myotonia, and muscular dystrophy are discussed. Neuromuscular junction disorders such as myasthenia gravis, Lambert-Eaton syndrome, and botulism are discussed also. Guillain-Barré syndrome and its variants are described. Motor neuron diseases, such as amyotrophic lateral sclerosis, are discussed.
Robert J. Gatchel +3 more
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Abstract Types of myopathy, myotonia, and muscular dystrophy are discussed. Neuromuscular junction disorders such as myasthenia gravis, Lambert-Eaton syndrome, and botulism are discussed also. Guillain-Barré syndrome and its variants are described. Motor neuron diseases, such as amyotrophic lateral sclerosis, are discussed.
Robert J. Gatchel +3 more
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Autoimmunity in Neuromuscular Disease
Annals of the New York Academy of Sciences, 1987SUMMARY AND CONCLUSIONSA number of confounding factors can be identified from the search for autoimmune mechanisms over the last 2 decades that may be relevant for future studies. (1) An apparently homogeneous clinical disorder may represent more than one disease process and thereby imply antibody/antigen heterogeneity as, for example, in MG with and ...
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1983
Whether spastic, athetotic, or ataxic, the child with CP is limited in his physical abilities. The spastic child may not be able to generate much muscle force or endure effort for a long time but can perform fine movements better than the athetotic child.
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Whether spastic, athetotic, or ataxic, the child with CP is limited in his physical abilities. The spastic child may not be able to generate much muscle force or endure effort for a long time but can perform fine movements better than the athetotic child.
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2023
Abstract Summary Blood gas homeostasis depends on adequate functioning of the respiratory muscles. Respiratory muscle function can be impaired by diseases or pathophysiological processes that cause weakness, while contractile activity is reduced physiologically during sleep (especially rapid eye movement sleep) and ...
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Abstract Summary Blood gas homeostasis depends on adequate functioning of the respiratory muscles. Respiratory muscle function can be impaired by diseases or pathophysiological processes that cause weakness, while contractile activity is reduced physiologically during sleep (especially rapid eye movement sleep) and ...
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2003
Abstract From an organizational standpoint, it is useful to begin with a classification of neuromuscular diseases. The classification presented here is not meant to be comprehensive, but to enumerate disorders which are commonly encountered. This is a standard classification modified from Walton et al.
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Abstract From an organizational standpoint, it is useful to begin with a classification of neuromuscular diseases. The classification presented here is not meant to be comprehensive, but to enumerate disorders which are commonly encountered. This is a standard classification modified from Walton et al.
openaire +2 more sources