Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology
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Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)Pharmacological interventions for improving respiratory function in amyotrophic lateral sclerosisCreatine for amyotrophic lateral sclerosis/motor neuron diseaseCreatine for amyotrophic lateral sclerosis/motor neuron diseaseEnteral tube feeding for amyotrophic lateral sclerosis/motor neuron diseaseQuo vadis motor neuron disease?A comprehensive review of amyotrophic lateral sclerosisComplementary and Alternative Therapies in Amyotrophic Lateral SclerosisQuality improvement in neurology: amyotrophic lateral sclerosis quality measures: report of the quality measurement and reporting subcommittee of the American Academy of NeurologyAmyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic TrialsQuality improvement in neurology: muscular dystrophy quality measuresA protocol to develop clinical guidelines for inclusion-body myositisCPAP and bi-level PAP therapy: new and established rolesClinical perspective on oxidative stress in sporadic amyotrophic lateral sclerosisSafety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trialDecreased Peak Expiratory Flow Associated with Muscle Fiber-Type Switching in Spinal and Bulbar Muscular Atrophy.Comprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis.Rehabilitation in amyotrophic lateral sclerosis: why it mattersIs survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients.Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach.Determinants of accepting non-invasive ventilation treatment in motor neurone disease: a quantitative analysis at point of needHypercaloric enteral nutrition in patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled phase 2 trialAdvances in Positive Airway Pressure Treatment Modalities for Hypoventilation SyndromesUsing respiratory rate and thoracic movement to assess respiratory insufficiency in amyotrophic lateral sclerosis: a preliminary study.Limb-onset amyotrophic lateral sclerosis patients visiting orthopedist show a longer time-to-diagnosis since symptom onset.Racial differences in motor neuron diseaseDexpramipexole is ineffective in two models of ALS related neurodegeneration.Weight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options.Survey of current enteral nutrition practices in treatment of amyotrophic lateral sclerosisCommunication Support for People with ALS.Advanced statistical methods to study the effects of gastric tube and non-invasive ventilation on functional decline and survival in amyotrophic lateral sclerosisPhase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial designMedical management of frontotemporal dementias: the importance of the caregiver in symptom assessment and guidance of treatment strategiesAnd the patient said: "let me be able to breathe and dream".Noninvasive ventilation improves sleep in amyotrophic lateral sclerosis: a prospective polysomnographic study.Multidisciplinary Interventions in Motor Neuron Disease.Palliative Care Issues in Amyotrophic Lateral Sclerosis: An Evidenced-Based Review.Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study.Moving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapiesHospitalizations due to respiratory failure in patients with Amyotrophic Lateral Sclerosis and their impact on survival: a population-based cohort study
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P2860
Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on October 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Practice parameter update: the ...... American Academy of Neurology
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Practice parameter update: the ...... American Academy of Neurology.
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type
label
Practice parameter update: the ...... American Academy of Neurology
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Practice parameter update: the ...... American Academy of Neurology.
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prefLabel
Practice parameter update: the ...... American Academy of Neurology
@en
Practice parameter update: the ...... American Academy of Neurology.
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P2093
P2860
P1433
P1476
Practice parameter update: the ...... American Academy of Neurology
@en
P2093
C E Jackson
C Shoesmith
E J Kasarskis
H Mitsumoto
J D England
J Rosenfeld
M J Strong
Quality Standards Subcommittee of the American Academy of Neurology
P2860
P304
P356
10.1212/WNL.0B013E3181BC0141
P407
P577
2009-10-01T00:00:00Z