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Neuromuscular Diseases

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 ...
B. Morrison
openaire   +3 more sources

Pediatric Neuromuscular Diseases

Pediatric Neurology, 2023
The diagnostic and referral workflow for children with neuromuscular disorders is evolving, particularly as newborn screening programs are expanding in tandem with novel therapeutic developments. However, for the children who present with symptoms and signs of potential neuromuscular disorders, anatomic localization, guided initially by careful history
Geetanjali Rathore, Peter B. Kang
openaire   +2 more sources

MRI in Neuromuscular Diseases: An Emerging Diagnostic Tool and Biomarker for Prognosis and Efficacy

Annals of Neurology, 2020
There is an unmet need to identify biomarkers sensitive to change in rare, slowly progressive neuromuscular diseases. Quantitative magnetic resonance imaging (MRI) of muscle may offer this opportunity, as it is noninvasive and can be carried out almost ...
J. Dahlqvist   +3 more
semanticscholar   +1 more source

Hereditary neuromuscular diseases

European Journal of Radiology, 2001
This 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
openaire   +3 more sources

Immunosuppressive and immunomodulatory therapies for neuromuscular diseases. Part II: New and novel agents

Muscle and Nerve, 2020
While traditional immunosuppressive and immunomodulatory therapies remain the cornerstone of immune‐mediated neuromuscular disease management, new and novel agents including antigen‐specific, monoclonal antibody drugs, have emerged as important treatment
C. Farmakidis   +3 more
semanticscholar   +1 more source

Neuromuscular Diseases

Neuropalliative Care, 2018
Maisha T. Robinson, Danny Estupinan
openaire   +2 more sources

Neuromuscular Diseases

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
openaire   +2 more sources

Autoimmunity in Neuromuscular Disease

Annals of the New York Academy of Sciences, 1987
SUMMARY 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 ...
openaire   +2 more sources

Health maintenance for adults with neuromuscular diseases on immunosuppression

Muscle and Nerve, 2019
Immunosuppressants are commonly used in the treatment of neuromuscular diseases. The use of these medications requires health maintenance screening and monitoring for multiple potential sides effects, which may be best conducted when the prescribing ...
S. Cartwright, M. Cartwright
semanticscholar   +1 more source

How useful is muscle ultrasound in the diagnostic workup of neuromuscular diseases?

Current Opinion in Neurology, 2018
Purpose of review This review focuses on developments in muscle ultrasound as a noninvasive and accurate tool for the diagnosis and follow-up of neuromuscular disease. It discusses current muscle ultrasound applications with already proven clinical value,
N. van Alfen   +2 more
semanticscholar   +1 more source

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