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Are Insulin and Metformin Really Protective on Amyotrophic Lateral Sclerosis by Blocking the Astrocytic Cx43 Channel? [PDF]
Chronic Dis Transl MedFinsterer J.
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CYP2D6 variants in amyotrophic lateral sclerosis: an association study of risk and survival
Vallikivi JK +5 more
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Retinal Imaging in Motor Neuron Disease – Amyotrophic Lateral Sclerosis: A Systematic Review
Ozzoude M +9 more
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Amyotrophic lateral sclerosis.
Current Opinion in Neurology, 2012The field of amyotrophic lateral sclerosis (ALS) has seen a number of remarkable advances during recent years that will be summarized in this review.In particular, the progress in the molecular neuropathology with the discovery of pathogenic mutations in TAR DNA binding protein (TARDBP), fused in sarcoma (FUS), ubiquilin2 (UBQLN2) and most recently ...
A. Ludolph +2 more
semanticscholar +3 more sources
Seminars in Neurology, 2014
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting 20,000 to 30,000 people in the United States. The mainstay of care of patients affected by this disease is supportive and given the multifaceted nature of their needs is provided most efficiently through multidisciplinary clinics that have shown to prolong ...
Rabia, Malik +2 more
openaire +3 more sources
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting 20,000 to 30,000 people in the United States. The mainstay of care of patients affected by this disease is supportive and given the multifaceted nature of their needs is provided most efficiently through multidisciplinary clinics that have shown to prolong ...
Rabia, Malik +2 more
openaire +3 more sources
The Lancet, 2007
Amyotrophic lateral sclerosis (known in the UK as motor neuron disease) is a devastating illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical features, diagnostic criteria, variant and mimic syndromes, genetic forms, and epidemiology.
J D, Mitchell, G D, Borasio
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Amyotrophic lateral sclerosis (known in the UK as motor neuron disease) is a devastating illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical features, diagnostic criteria, variant and mimic syndromes, genetic forms, and epidemiology.
J D, Mitchell, G D, Borasio
openaire +3 more sources
Diagnostic Utility of Gold Coast Criteria in Amyotrophic Lateral Sclerosis
Annals of Neurology, 2021The diagnosis of amyotrophic lateral sclerosis (ALS) remains problematic, with current diagnostic criteria (revised El Escorial [rEEC] and Awaji) being complex and prone to error.
Andrew P Hannaford +7 more
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