about
Use of the short form health survey (SF-36) in patients with amyotrophic lateral sclerosis: tests of data quality, score reliability, response rate and scaling assumptions.Post-traumatic amnesia and confusional state: hazards of retrospective assessment.Awaji criteria improves the diagnostic sensitivity in amyotrophic lateral sclerosis: A systematic review using individual patient data.Neurologic complications of craniovertebral dislocation.Hughlings Jackson's clinical research: evidence from contemporary documents.Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy.Lockhart Clarke's contribution to the description of amyotrophic lateral sclerosis.Amyotrophic lateral sclerosis: a consensus viewpoint on designing and implementing a clinical trial.The Neurophysiological Index in ALS.Controversies and priorities in amyotrophic lateral sclerosis.Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials.Clinical trials in ALS: a review of the role of clinical and neurophysiological measurements.Rectal hyposensitivity.Electrodiagnostic criteria for diagnosis of ALS.Amyotrophic lateral sclerosis: an update.Why are upper motor neuron signs difficult to elicit in amyotrophic lateral sclerosis?Awaji criteria for the diagnosis of amyotrophic lateral sclerosis:a systematic review.Amyotrophic lateral sclerosis: a long preclinical period?Motoneuron firing in amyotrophic lateral sclerosis (ALS)The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odysseyLower motor neuron dysfunction in ALS.John Hughlings Jackson (1835-1911): An adornment to the London Hospital.Fasciculation in amyotrophic lateral sclerosis: origin and pathophysiological relevance.Sensitivity of MUP parameters in detecting change in early ALS.Clinical and neurophysiological evaluation of progression in amyotrophic lateral sclerosis.Awaji diagnostic algorithm increases sensitivity of El Escorial criteria for ALS diagnosis.Apraxia contributes to the motor deficit in Parkinson's Disease and multiple system atrophy.Sacrocolpopexy may cause difficult defecation by inhibiting the external opening out mechanism.Does surgery accelerate progression of amyotrophic lateral sclerosis?Fasciculation potentials and earliest changes in motor unit physiology in ALS.Controversies about databases.F-Waves and the corticospinal lesion in amyotrophic lateral sclerosis.Motor responses evoked by transcranial magnetic stimulation and peripheral nerve stimulation in the ulnar innervation in amyotrophic lateral sclerosis: the effect of upper and lower motor neuron lesion.Survey of non-invasive ventilation use in ALS in Britain.Origin of fasciculations in amyotrophic lateral sclerosis and benign fasciculation syndrome.Kinnier Wilson's puzzling features of amyotrophic lateral sclerosis.Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.How does ALS spread between neurones in the CNS?New ideas for therapy in ALS.Diaphragm motor responses to phrenic nerve stimulation in ALS: Surface and needle recordings.
P50
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P50
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hulumtues
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հետազոտող
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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Michael Swash
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0000 0001 1063 9156
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1939-01-29T00:00:00Z
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