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Amyotrophic lateral sclerosis.
Published 2011“…Amyotrophic lateral sclerosis (ALS) is an idiopathic, fatal neurodegenerative disease of the human motor system. …”
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Dysautonomia in Amyotrophic Lateral Sclerosis
Published 2023-10-01Subjects: “…amyotrophic lateral sclerosis…”
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Complicated amyotrophic lateral sclerosis
Published 2024-01-01“…Amyotrophic lateral sclerosis is a degenerative neuromuscular disease, it originates when the cells of the nervous system called motoneurons gradually decrease their functioning and die, causing a progressive muscle paralysis of poor prognosis, with low incidence and prevalence of 3 to 5 per 100000 inhabitants and affects people between 40 and 70 years. …”
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Epidemiology of Amyotrophic Lateral Sclerosis
Published 2020-09-01“…There has been an increase in studies on amyotrophic lateral sclerosis (ALS) in the last thirty years. …”
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Kinesitherapy in amyotrophic lateral sclerosis
Published 2017-12-01Subjects: “…amyotrophic lateral sclerosis…”
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Kinesitherapy in amyotrophic lateral sclerosis
Published 2017-12-01Subjects: “…amyotrophic lateral sclerosis, nervous system, kinesitherapy, neuroprotection…”
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Amyotrophic lateral sclerosis: update
Published 2016-04-01Subjects: “…Amyotrophic Lateral Sclerosis…”
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Pain in amyotrophic lateral sclerosis
Published 2019-08-01Subjects: “…amyotrophic lateral sclerosis…”
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Biomarkers in amyotrophic lateral sclerosis.
Published 2009“…Amyotrophic lateral sclerosis (ALS; motor neuron disease) is a relentlessly progressive disorder. …”
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Neuroimaging in amyotrophic lateral sclerosis.
Published 2012“…The catastrophic system failure in amyotrophic lateral sclerosis is characterized by progressive neurodegeneration within the corticospinal tracts, brainstem nuclei and spinal cord anterior horns, with an extra-motor pathology that has overlap with frontotemporal dementia. …”
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The genetics of amyotrophic lateral sclerosis
Published 2009“…Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterised clinically by rapidly progressive paralysis leading ultimately to death from respiratory failure. …”
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Sensory Involvement in Amyotrophic Lateral Sclerosis
Published 2022-12-01“…Although amyotrophic lateral sclerosis (ALS) is pre-eminently a motor disease, the existence of non-motor manifestations, including sensory involvement, has been described in the last few years. …”
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Molecular Research on Amyotrophic Lateral Sclerosis
Published 2022-10-01“…Amyotrophic Lateral Sclerosis (ALS) is a rare, progressive, lethal, and degenerative disease of motor neurons for which there is no treatment currently available [...]…”
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Amyotrophic lateral sclerosis with frontotemporal dementia
Published 2010-09-01Subjects: “…amyotrophic lateral sclerosis…”
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Deontological aspects of the amyotrophic lateral sclerosis
Published 2018-01-01“…The article discusses the positive and negative aspects of fully informing patients with amyotrophic lateral sclerosis about the fatal diagnosis. There are 2 clinical cases reflecting different approaches of this complex issue: full awareness and concealment of the diagnosis.…”
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Amyotrophic Lateral Sclerosis: Advances and Prospects
Published 2023-08-01“…The <i>JCM</i> Topical Collection “Amyotrophic Lateral Sclerosis: Latest Advances and Prospects” started in 2020 and currently includes 11 publications reflecting a broad range of clinical research areas in the ALS field [...]…”
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Management of patients with amyotrophic lateral sclerosis
Published 2005-10-01Subjects: Get full text
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