Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register - Test2 - elhamkhani - TriplyDB

Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

http://www.wikidata.org/entity/Q22306505

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Amyotrophic lateral sclerosis: considerations on diagnostic criteria Amyotrophic lateral sclerosis mimic syndromes Recent advances in amyotrophic lateral sclerosis A comprehensive review of amyotrophic lateral sclerosis Amyotrophic lateral sclerosis multiprotein biomarkers in peripheral blood mononuclear cells Neuroimaging to investigate multisystem involvement and provide biomarkers in amyotrophic lateral sclerosis Electrodiagnostic studies in amyotrophic lateral sclerosis and other motor neuron disorders.The 12 year prognosis of unilateral functional weakness and sensory disturbance.The management of motor neurone disease.Amyotrophic lateral sclerosis: update and new developments.The epidemiology and treatment of ALS: focus on the heterogeneity of the disease and critical appraisal of therapeutic trials.Management guidelines for motor neurone disease patients on non-invasive ventilation at home.Pearls & Oy-sters: The importance of atypical features and tracking progression in patients misdiagnosed with ALS Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group.EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force.MicroRNAs as potential circulating biomarkers for amyotrophic lateral sclerosis.Time to diagnosis in the National Registry of Veterans with Amyotrophic Lateral Sclerosis.Multimodal structural MRI in the diagnosis of motor neuron diseases Cervicothoracic intradural arachnoid cyst misdiagnosed as motor neuron disease.Diagnosing motor neurone disease.SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in management.Early diagnosis of amyotrophic lateral sclerosis mimic syndromes: pros and cons of current clinical diagnostic criteria.Prospective, blind study of the triple stimulation technique in the diagnosis of ALS.Is firstly diagnosed ALS really ALS? Results of a population-based study with long-term follow-up.The El Escorial criteria: Strengths and weaknesses Amyotrophic lateral sclerosis: Analysis of ALS cases in a predominantly admixed population of Ecuador Motor nerve biopsy: Clinical usefulness and histopathological criteria

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P2860

Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

http://www.wikidata.org/entity/Q22306505

description

1996 nî lūn-bûn

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1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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1996 թվականի փետրվարին հրատարակված գիտական հոդված

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1996年の論文

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1996年論文

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Avoiding false positive diagno ...... Motor Neuron Disease Register

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Avoiding false positive diagno ...... Motor Neuron Disease Register

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Avoiding false positive diagno ...... Motor Neuron Disease Register

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Journal of Neurology, Neurosurgery and Psychiatry

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Chancellor AM

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Davenport RJ

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Swingler RJ

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Warlow CP

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P2860

Frontal lobe dementia and motor neuron disease.

Utility of Scottish morbidity and mortality data for epidemiological studies of motor neuron disease.

Inter-relation between "classic" motor neuron disease and frontotemporal dementia: neuropsychological and single photon emission computed tomography study

Multifocal motor neuropathy: response to human immune globulin.

Patient resistance and prognosis in amyotrophic lateral sclerosis.

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2

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60

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14492994

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8708642

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1073793

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