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Expression of HLA-DR in pheripheral nerve of amyotrophic lateral sclerosis
Published 1994-12-01“…To investigate the possibility of local antigen presentation within the peripheral nerve in amyotrophic lateral sclerosis (ALS), cryostat sections of 83 peripheral nerve biopsies were stained for the demonstration of HLA-DR using a monoclonal antibody. …”
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222
Status of biomarker development for frontotemporal dementia and amyotrophic lateral sclerosis
Published 2024-01-01Get full text
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223
Janus kinase inhibitors are potential therapeutics for amyotrophic lateral sclerosis
Published 2023-10-01Subjects: Get full text
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224
Hydrogen Peroxide and Amyotrophic Lateral Sclerosis: From Biochemistry to Pathophysiology
Published 2021-12-01Subjects: Get full text
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225
Predictors of Depression in Caucasian Patients with Amyotrophic Lateral Sclerosis in Romania
Published 2020-07-01Subjects: Get full text
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226
Familial neurodegenerative disease with parkinsonism syndrome and amyotrophic lateral sclerosis
Published 2018-11-01Subjects: Get full text
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227
The Biogenesis of miRNAs and Their Role in the Development of Amyotrophic Lateral Sclerosis
Published 2022-02-01Subjects: “…amyotrophic lateral sclerosis…”
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228
Acoustic features of impaired articulation due to amyotrophic lateral sclerosis
Published 2018Get full text
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229
Smoking and risk for amyotrophic lateral sclerosis: analysis of the EPIC cohort.
Published 2009“…OBJECTIVE: Cigarette smoking has been reported as "probable" risk factor for Amyotrophic Lateral Sclerosis (ALS), a poorly understood disease in terms of aetiology. …”
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230
Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis
Published 2018“…<p>The adult neurodegenerative disorder amyotrophic lateral sclerosis (ALS) is unmistakeable from clinical descriptions now more than a century old.1 Neither the site of symptom onset in ALS2 nor pattern of symptom spread3–5 is truly random. …”
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231
The diagnostic pathway and prognosis in bulbar-onset amyotrophic lateral sclerosis.
Published 2010“…BACKGROUND: Despite the inevitability of disease progression in amyotrophic lateral sclerosis, there is a high degree of prognostic heterogeneity in all subtypes. …”
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232
Advancing mechanistic understanding and biomarker development in amyotrophic lateral sclerosis
Published 2021“…<br><strong>Introduction<br></strong> Proteomic analysis has contributed significantly to the study of the neurodegenerative disease amyotrophic lateral sclerosis (ALS). It has helped to define the pathological change common to nearly all cases, namely intracellular aggregates of phosphorylated TDP-43, shifting the focus of pathogenesis in ALS toward RNA biology. …”
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A case of celiac disease mimicking amyotrophic lateral sclerosis.
Published 2007“…DIAGNOSIS: Celiac disease with neurological involvement, mimicking amyotrophic lateral sclerosis. MANAGEMENT: Strict gluten-free diet.…”
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234
Multicenter evaluation of neurofilaments in early symptomatic amyotrophic lateral sclerosis
Published 2017Journal article -
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Oculomotor dysfunction in amyotrophic lateral sclerosis: a comprehensive review.
Published 2011“…Although traditionally regarded as spared, a range of oculomotor dysfunction has been recorded in patients with amyotrophic lateral sclerosis (ALS). Most frequent is ophthalmoparesis, particularly in patients with prolonged survival; however, pursuit, nystagmus, and saccadic impairments have also been reported. …”
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The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis.
Published 2015Journal article -
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Unmasking of incipient amyotrophic lateral sclerosis by botulinum toxin therapy
Published 2013Journal article -
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Autoimmune disease preceding amyotrophic lateral sclerosis: an epidemiologic study.
Published 2013“…OBJECTIVE: To study whether the risk of amyotrophic lateral sclerosis (ALS) is increased in people with prior autoimmune disease. …”
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Volumetric cortical loss in sporadic and familial amyotrophic lateral sclerosis.
Published 2007Journal article -
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Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis?
Published 2012“…Amyotrophic lateral sclerosis (ALS) is typically regarded as a sporadic neurodegenerative disorder that results in a catastrophic failure of the motor system, with characteristically variable involvement of upper and lower motor neuronal populations. …”
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