Search Results - "TISON, François"
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The natural history of multiple system atrophy: a prospective European cohort study
Published in Lancet neurology (01-03-2013)“…Summary Background Multiple system atrophy (MSA) is a fatal and still poorly understood degenerative movement disorder that is characterised by autonomic…”
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Pathophysiology of L-dopa-induced motor and non-motor complications in Parkinson's disease
Published in Progress in neurobiology (01-09-2015)“…Involuntary movements, or dyskinesia, represent a debilitating complication of levodopa (L-dopa) therapy for Parkinson's disease (PD). L-dopa-induced…”
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Disease progression and prognostic factors in multiple system atrophy: A prospective cohort study
Published in Neurobiology of disease (01-06-2020)“…Multiple system atrophy (MSA) is a rare neurodegenerative disease, with limited understanding of disease progression and prognostic factors. We leveraged the…”
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A Phase 2A Trial of the Novel mGluR5-Negative Allosteric Modulator Dipraglurant for Levodopa-Induced Dyskinesia in Parkinson's Disease
Published in Movement disorders (01-09-2016)“…ABSTRACT Background The metabotropic glutamate receptor 5‐negative allosteric modulator dipraglurant reduces levodopa‐induced dyskinesia in the MPTP‐macaque…”
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Multiple System Atrophy: Recent Developments and Future Perspectives
Published in Movement disorders (01-11-2019)“…Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disorder characterized by a variable combination of parkinsonism, cerebellar impairment,…”
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Stridor in multiple system atrophy: Consensus statement on diagnosis, prognosis, and treatment
Published in Neurology (01-10-2019)“…Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by a combination of autonomic failure, cerebellar ataxia, and parkinsonism…”
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A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies
Published in Brain (London, England : 1878) (01-06-2017)“…Autosomal dominant cerebellar ataxias have a marked heterogeneous genetic background, with mutations in 34 genes identified so far. This large amount of…”
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International validation of a behavioral scale in Parkinson's disease without dementia
Published in Movement disorders (15-04-2015)“…The “Ardouin Scale of Behavior in Parkinson's Disease” is a new instrument specifically designed for assessing mood and behavior with a view to quantifying…”
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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
Published in Nature genetics (01-06-2015)“…Jean-Luc Battini, Giovanni Coppola and colleagues identify XPR1 mutations in several families with primary brain calcification. They further show that these…”
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Trends in Prevalence of Dementia in French Farmers from Two Epidemiological Cohorts
Published in Journal of the American Geriatrics Society (JAGS) (01-02-2017)“…Objectives To determine the prevalence of dementia and cognitive impairment in older people across generations. Design Two prospective cohort studies…”
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Withdrawing amantadine in dyskinetic patients with Parkinson disease: The AMANDYSK trial
Published in Neurology (28-01-2014)“…OBJECTIVE:The AMANDYSK trial was designed to assess long-term efficacy of chronic treatment with amantadine in patients with Parkinson disease (PD) and…”
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Characterization of Recessive Parkinson Disease in a Large Multicenter Study
Published in Annals of neurology (01-10-2020)“…Studies of the phenotype and population distribution of rare genetic forms of parkinsonism are required, now that gene‐targeting approaches for Parkinson…”
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Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia
Published in Journal of neurology (01-05-2021)“…Background STUB1 has been first associated with autosomal recessive (SCAR16, MIM# 615768) and later with dominant forms of ataxia (SCA48, MIM# 618093)…”
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Characteristics in limbic encephalitis with anti–adenylate kinase 5 autoantibodies
Published in Neurology (07-02-2017)“…OBJECTIVE:To report 10 patients with limbic encephalitis (LE) and adenylate kinase 5 autoantibodies (AK5-Abs). METHODS:We conducted a retrospective study in a…”
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Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort
Published in Frontiers in neurology (28-07-2020)“…, and are unequivocally associated with autosomal dominant Parkinson's disease (PD). We evaluated the prevalence of , and mutations and associated clinical…”
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The late stage of Parkinson's –results of a large multinational study on motor and non-motor complications
Published in Parkinsonism & related disorders (01-06-2020)“…There is little information on the late stages of parkinsonism. We conducted a multicentre study in 692 patients with late stage parkinsonism in six European…”
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Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA‐FLUO Trial
Published in Movement disorders (01-07-2021)“…ABSTRACT Background There are no effective treatments for multiple system atrophy (MSA). Objective The objective of this study was to assess the efficacy and…”
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Genome sequence analyses identify novel risk loci for multiple system atrophy
Published in Neuron (Cambridge, Mass.) (03-07-2024)“…Multiple system atrophy (MSA) is an adult-onset, sporadic synucleinopathy characterized by parkinsonism, cerebellar ataxia, and dysautonomia. The genetic…”
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Care of Late‐Stage Parkinsonism: Resource Utilization of the Disease in Five European Countries
Published in Movement disorders (01-03-2024)“…Background Parkinson's disease (PD) is a neurodegenerative disease that leads to progressive disability. Cost studies have mainly explored the early stages of…”
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Dysphagia in multiple system atrophy consensus statement on diagnosis, prognosis and treatment
Published in Parkinsonism & related disorders (01-05-2021)“…Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by a combination of autonomic failure plus cerebellar syndrome and/or parkinsonism…”
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