Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study.
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Dietary BMAA exposure in an amyotrophic lateral sclerosis cluster from southern FranceFrom animal models to human disease: a genetic approach for personalized medicine in ALSAmyotrophic lateral sclerosis mimic syndromesQuo vadis motor neuron disease?Amyotrophic Lateral Sclerosis: New Perpectives and UpdateLigand binding and aggregation of pathogenic SOD1Monitoring CSF proteome alterations in amyotrophic lateral sclerosis: obstacles and perspectives in translating a novel marker panel to the clinicChemokine MIP-2/CXCL2, acting on CXCR2, induces motor neuron death in primary culturesElectrodiagnosis in Persons With Amyotrophic Lateral SclerosisDiscriminant ability of the Eating Assessment Tool-10 to detect aspiration in individuals with amyotrophic lateral sclerosis.Neuroimaging to investigate multisystem involvement and provide biomarkers in amyotrophic lateral sclerosisWidespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral SclerosisVariation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis.Incidence of amyotrophic lateral sclerosis in Europe.The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.Utility of dissociated intrinsic hand muscle atrophy in the diagnosis of amyotrophic lateral sclerosisALS-Plus syndrome: non-pyramidal features in a large ALS cohort.Survival analysis of irish amyotrophic lateral sclerosis patients diagnosed from 1995-2010.Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research.Genetic overlap between apparently sporadic motor neuron diseases.Copper and zinc metallation status of copper-zinc superoxide dismutase from amyotrophic lateral sclerosis transgenic mice.Models of care for motor neuron disease: setting standards.The Role of immune and inflammatory mechanisms in ALS.The effect of autologous bone marrow mononuclear cell transplantation on the survival duration in Amyotrophic Lateral Sclerosis - a retrospective controlled study.Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study.Results of Florida's Amyotrophic Lateral Sclerosis Surveillance Project, 2009-2011.New considerations in the design of clinical trials for amyotrophic lateral sclerosisEpidemiology and surveillance of amyotrophic lateral sclerosis in two large metropolitan areas in California.Controversies and priorities in amyotrophic lateral sclerosis.Physical decline and quality of life in amyotrophic lateral sclerosis.Moving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapiesForced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic populationKlinefelter's syndrome associated with progressive muscular atrophy simulating Kennedy's diseaseThe Awaji criteria increases the diagnostic sensitivity of the revised El Escorial criteria for amyotrophic lateral sclerosis diagnosis in a Chinese populationEngaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionalsPrognostic factors in ALS: A critical reviewState and metropolitan area-based amyotrophic lateral sclerosis (ALS) surveillance.Decline in daily running distance presages disease onset in a mouse model of ALS.ALS drug development: reflections from the past and a way forwardA timeline for predicting durable medical equipment needs and interventions for amyotrophic lateral sclerosis patients.
P2860
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P2860
Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh-hant
name
Clinical features of amyotroph ...... ria: A population-based study.
@en
Clinical features of amyotroph ...... ria: A population-based study.
@nl
type
label
Clinical features of amyotroph ...... ria: A population-based study.
@en
Clinical features of amyotroph ...... ria: A population-based study.
@nl
prefLabel
Clinical features of amyotroph ...... ria: A population-based study.
@en
Clinical features of amyotroph ...... ria: A population-based study.
@nl
P2093
P1433
P1476
Clinical features of amyotroph ...... ria: A population-based study.
@en
P2093
P304
P356
10.1001/ARCHNEUR.57.8.1171
P577
2000-08-01T00:00:00Z