A multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland

scientific article published on 30 December 2014

A multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/JNNP-2014-309601
P698PubMed publication ID25550416
P5875ResearchGate publication ID270290095

P50authorOrla HardimanQ30423350
Katy TobinQ40015163
James RooneyQ58400289
Susan ByrneQ61827445
Mark HeverinQ89957359
P2093author name stringAlison Dick
Colette Donaghy
P2860cites workSurvival analysis of irish amyotrophic lateral sclerosis patients diagnosed from 1995-2010.Q34375695
Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996-2000.Q35476043
The effect of non-invasive positive pressure ventilation (NIPPV) on cognitive function in amyotrophic lateral sclerosis (ALS): a prospective studyQ35572459
Prognostic factors in ALS: A critical reviewQ36447824
The natural history of motor neuron disease: assessing the impact of specialist careQ38014082
The epidemiology of motor neuron disease in Northern Ireland using capture-recapture methodologyQ39863626
EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosing and clinical care of patients and relativesQ46832663
Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomised controlled trialQ47652452
Cluster RCT of case management on patients' quality of life and caregiver strain in ALS.Q48127223
Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia.Q51014067
Evidence of an environmental effect on survival in ALS.Q51721412
Multidisciplinary ALS care improves quality of life in patients with ALS.Q51924828
Amyotrophic lateral sclerosisQ55877676
P433issue5
P407language of work or nameEnglishQ1860
P921main subjectamyotrophic lateral sclerosisQ206901
P304page(s)496-501
P577publication date2014-12-30
P1433published inJournal of Neurology, Neurosurgery and PsychiatryQ1599804
P1476titleA multidisciplinary clinic approach improves survival in ALS: a comparative study of ALS in Ireland and Northern Ireland
P478volume86

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cites work (P2860)
Q38557374"Anything that makes life's journey better." Exploring the use of digital technology by people living with motor neurone disease.
Q38617893A Qualitative Study of Multidisciplinary ALS Clinic Use in the United States
Q37471676A clinical tool for predicting survival in ALS.
Q64894086A multidisciplinary clinic approach to improve physician-related diagnostic delay for patients with axial spondyloarthritis: a retrospective study.
Q47274912A spatial analysis of amyotrophic lateral sclerosis (ALS) cases in the United States and their proximity to multidisciplinary ALS clinics, 2013.
Q92339532Adjusted cost analysis of video televisits for the care of people with amyotrophic lateral sclerosis
Q56531746Amyotrophic lateral sclerosis
Q56531747Amyotrophic lateral sclerosis
Q38715468Amyotrophic lateral sclerosis and frontotemporal dementia: distinct and overlapping changes in eating behaviour and metabolism
Q33734415Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach
Q47590248Apathy is associated with poor prognosis in amyotrophic lateral sclerosis
Q64228443Clinical Measures of Bulbar Dysfunction in ALS
Q40719786Cognition and eating behavior in amyotrophic lateral sclerosis: effect on survival
Q91660078Communicating psychosocial well-being in motor neurone disease to staff: results from a World Café approach
Q40380484Compliance with recommendations made in a multidisciplinary ALS clinic
Q39386238Developing multidisciplinary clinics for neuromuscular care and research.
Q39289468Development of patient decision support tools for motor neuron disease using stakeholder consultation: a study protocol
Q30691863Discriminant ability of the Eating Assessment Tool-10 to detect aspiration in individuals with amyotrophic lateral sclerosis.
Q92537437Editorial: Biomarkers and Clinical Indicators in Motor Neuron Disease
Q47742878End-of-life Characteristics and Palliative Care Provision for Patients With Motor Neuron Disease
Q58583906Epidemiology of ALS in Korea using nationwide big data
Q49691472Experience with telemedicine in a multi-disciplinary ALS clinic
Q39252157Factors predicting survival in ALS: a multicenter Italian study
Q37728216From first symptoms to diagnosis of amyotrophic lateral sclerosis: perspectives of an Irish informal caregiver cohort-a thematic analysis
Q64274786High-frequency motor rehabilitation in amyotrophic lateral sclerosis: a randomized clinical trial
Q46604820Improving symptom management for people with amyotrophic lateral sclerosis
Q50545364Incorporation of telehealth into a multidisciplinary ALS Clinic: feasibility and acceptability.
Q33786829Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy
Q58787868Maximizing the Survival of Amyotrophic Lateral Sclerosis Patients: Current Perspectives
Q39036805Motor neuron disease: biomarker development for an expanding cerebral syndrome
Q38597450Motor neuron disease: current management and future prospects
Q64960348Palliative care for patients with motor neurone disease: current challenges.
Q61812640Palliative care in motor neurone disease: where are we now?
Q35877457Patient journey to a specialist amyotrophic lateral sclerosis multidisciplinary clinic: an exploratory study
Q57488027Patient perspectives on transitioning to amyotrophic lateral sclerosis multidisciplinary clinics
Q49818063Patient-centered decision making in amyotrophic lateral sclerosis: where are we?
Q37164599Patient-reported problematic symptoms in an ALS treatment trial.
Q93089769Provincial Differences in the Diagnosis and Care of Amyotrophic Lateral Sclerosis
Q26749521Recent advances in amyotrophic lateral sclerosis
Q55134199Referral bias in ALS epidemiological studies.
Q93147168Retrospective longitudinal study of ALS in Cyprus: Clinical characteristics, management and survival
Q48101521Riluzole and other prognostic factors in ALS: a population-based registry study in Italy
Q34537070Supportive and symptomatic management of amyotrophic lateral sclerosis
Q39795426Survival analysis of geospatial factors in the Irish ALS cohort
Q92236845Survival benefit of multidisciplinary care in amyotrophic lateral sclerosis in Spain: association with noninvasive mechanical ventilation
Q33568729Survival prediction in Amyotrophic lateral sclerosis based on MRI measures and clinical characteristics
Q36293991The Awaji criteria increases the diagnostic sensitivity of the revised El Escorial criteria for amyotrophic lateral sclerosis diagnosis in a Chinese population
Q57798758The Multiple Sclerosis Care Unit
Q39218891The benefit of evolving multidisciplinary care in ALS: a diagnostic cohort survival comparison
Q47370892The development of the UK National Institute of Health and Care Excellence evidence-based clinical guidelines on motor neurone disease
Q50347043The evaluation of bulbar dysfunction in amyotrophic lateral sclerosis: survey of clinical practice patterns in the United States
Q33825530The path to specialist multidisciplinary care in amyotrophic lateral sclerosis: A population- based study of consultations, interventions and costs
Q35973665Using technology to improve access to specialist care in amyotrophic lateral sclerosis: A systematic review
Q89618542What is rehabilitation? An empirical investigation leading to an evidence-based description

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