Search Results - "Gelinas, Deborah F."
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Immunoglobulin administration for the treatment of CIDP: IVIG or SCIG?
Published in Journal of the neurological sciences (15-01-2020)“…Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired neurological disorder characterized clinically by weakness and impaired sensory…”
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MCP-1 chemokine receptor CCR2 is decreased on circulating monocytes in sporadic amyotrophic lateral sclerosis (sALS)
Published in Journal of neuroimmunology (01-10-2006)“…Recent studies suggest that monocyte activation may play a role in ALS pathogenesis. Therefore, monocyte CCR2, the receptor for monocyte chemoattractant…”
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Provisional best practices guidelines for the evaluation of bulbar dysfunction in amyotrophic lateral sclerosis
Published in Muscle & nerve (01-05-2019)“…Introduction: Universally established comprehensive clinical bulbar scales objectively assessing disease progression in amyotrophic lateral sclerosis (ALS) are…”
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Best practices protocol for the evaluation of bulbar dysfunction: summary recommendations from the NEALS bulbar subcommittee symposium
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (01-05-2018)“…The aim of this Symposium was to develop a consensus based, bulbar assessment protocol for implementation within NEALS clinics. A one-day symposium, held in…”
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Journal Article -
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Evidence for systemic immune system alterations in sporadic amyotrophic lateral sclerosis (sALS)
Published in Journal of neuroimmunology (01-02-2005)“…Sporadic amyotrophic lateral sclerosis (sALS) is a progressive neuroinflammatory disease of spinal cord motor neurons of unclear etiology. Blood from 38…”
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Journal Article -
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Hope in palliative care: from narcissism to self-transcendence in amyotrophic lateral sclerosis
Published in Journal of palliative medicine (01-04-2008)“…The concept of hope in palliative care is an important and neglected area of research. Amyotrophic lateral sclerosis (ALS), a progressive degenerative motor…”
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Amyotrophic lateral sclerosis
Published 2004“…ALS is not a curable disease, but it is a treatable one. Treatments are now available that can make a major difference in prolonging life and enhancing the…”
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"You have shown me my end": Attitudes toward presymptomatic testing for familial amyotrophic lateral sclerosis
Published in American journal of medical genetics. Part A (01-09-2004)“…Amyotrophic lateral sclerosis (ALS) is a lethal degenerative motor neuron disease. Approximately, 5–10% of cases of ALS are familial (FALS), inherited…”
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Quality of life for ventilator-dependent ALS patients and their caregivers
Published in Journal of the neurological sciences (01-10-1998)“…Seven ventilator-dependent ALS patients and eleven caregivers were interviewed in order to assess the impact of ventilator-dependence on patients and their…”
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Journal Article Conference Proceeding -
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Pulmonary function screening
Published in Seminars in neurology (01-03-2003)“…Patients who suffer from neuromuscular diseases often have complications from respiratory insufficiencies. Some neuromuscular diseases, for example Landry…”
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Creatine monohydrate in ALS: Effects on strength, fatigue, respiratory status and ALSFRS
Published in Amyotrophic lateral sclerosis (01-01-2008)“…Our objective was to determine the effect of creatine monohydrate on disease progression in patients with amyotrophic lateral sclerosis (ALS). One hundred and…”
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A comparison of maximal inspiratory pressure and forced vital capacity as potential criteria for initiating non-invasive ventilation in amyotrophic lateral sclerosis
Published in Amyotrophic lateral sclerosis (2007)“…Using a retrospective analysis of 161 patients with amyotrophic lateral sclerosis (ALS) from the Western ALS study group (WALS) database, the sensitivity of…”
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Vital capacity as an efficacy measure: Summary
Published in Amyotrophic lateral sclerosis and other motor neuron disorders (01-01-2002)Get full text
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Riluzole
Published in Amyotrophic lateral sclerosis and other motor neuron disorders (2000)Get full text
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Patient and caregiver communications and decisions
Published in Neurology (01-04-1997)Get full text
Conference Proceeding Journal Article -
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Measurement of Health-Related Quality of Life in Patients with Amyotrophic Lateral Sclerosis in Clinical Trials of New Therapies
Published in Medical care (01-01-1999)“…Objectives. Recent trials of amyotrophic lateral sclerosis (ALS) therapies have included the Sickness Impact Profile (SIP) to evaluate health-related quality…”
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RESPIRATORY COMPLICATIONS OF AMYOTROPHIC LATERAL SCLEROSIS: SYMPTOMS, SIGNS, DIAGNOSIS, AND TREATMENT
Published in Continuum (Minneapolis, Minn.) (01-08-2002)“…Amyotrophic lateral sclerosis (ALS) is a progressively paralyzing disease resulting in death, usually due to respiratory complications. Signs and symptoms of…”
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ALS standard of care consensus
Published in Neurology (01-04-1997)Get full text
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Cost effectiveness of recombinant human insulin-like growth factor I therapy in patients with ALS
Published in PharmacoEconomics (01-02-1999)“…Amyotrophic lateral sclerosis (ALS) is a fatal, degenerative neuromuscular disease characterised by a progressive loss of voluntary motor activity. Recombinant…”
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Journal Article -
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Best practices protocol for the evaluation of bulbar dysfunction: summary recommendations from the NEALS bulbar subcommittee symposium
Published in Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (03-04-2018)“…Objective: The aim of this Symposium was to develop a consensus based, bulbar assessment protocol for implementation within NEALS clinics. Methods: A one-day…”
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