Exploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment

scientific article published in August 2017

Exploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1080/21678421.2017.1353098
P698PubMed publication ID28762856

P50authorDidier HannequinQ32424966
Pierre-Marie PreuxQ49996439
Benoit MarinQ56862589
Pierre ClavelouQ72631651
Philippe CorciaQ77535028
P2093author name stringChristine Tranchant
William Camu
Fausto Viader
Philippe Couratier
Jean-Christophe Antoine
Marie Nicol
Véronique Danel-Brunaud
Geraldine Lautrette
Katell Beauvais
Bello Hamidou
Giroud Maurice
Marie-Christine Arnes-Bes
P2860cites workPhenotypic heterogeneity of amyotrophic lateral sclerosis: a population based studyQ22306516
Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND)Q24201081
Natural history and clinical features of the flail arm and flail leg ALS variantsQ24647753
Phase II/III randomized trial of TCH346 in patients with ALSQ28241484
The relationship between tirasemtiv serum concentration and functional outcomes in patients with ALSQ28296729
Consensus guidelines for the design and implementation of clinical trials in ALS. World Federation of Neurology committee on ResearchQ33762409
Incidence of amyotrophic lateral sclerosis in EuropeQ33774202
Safety and efficacy of ceftriaxone for amyotrophic lateral sclerosis: a multi-stage, randomised, double-blind, placebo-controlled trialQ34436090
Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial.Q34584573
Confirmatory double-blind, parallel-group, placebo-controlled study of efficacy and safety of edaravone (MCI-186) in amyotrophic lateral sclerosis patientsQ34699979
The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onsetQ37107393
Clinical trials in amyotrophic lateral sclerosis: why so many negative trials and how can trials be improved?Q38260277
Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trialQ39344567
Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosisQ42912800
Glatiramer acetate has no impact on disease progression in ALS at 40 mg/day: a double- blind, randomized, multicentre, placebo-controlled trialQ43239620
A confirmatory dose-ranging study of riluzole in ALS. ALS/Riluzole Study Group-II.Q43991574
A randomized sequential trial of creatine in amyotrophic lateral sclerosisQ44383439
Motor cortex stimulation for ALS: a double blind placebo-controlled studyQ44804216
Modeling drop-outs in amyotrophic lateral sclerosis.Q45906274
Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosisQ46657553
Pentoxifylline in ALS: a double-blind, randomized, multicenter, placebo-controlled trialQ46886269
Pilot trial of clenbuterol in spinal and bulbar muscular atrophyQ46959815
The ALSFRSr predicts survival time in an ALS clinic populationQ47867763
What does the ALSFRS-R really measure? A longitudinal and survival analysis of functional dimension subscores in amyotrophic lateral sclerosisQ48033371
A randomized controlled clinical trial of growth hormone in amyotrophic lateral sclerosis: clinical, neuroimaging, and hormonal resultsQ49124072
The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).Q53535985
Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS.Q55041563
The effects of dexpramipexole (KNS-760704) in individuals with amyotrophic lateral sclerosisQ56773744
A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosisQ57666978
Functional scales: SummaryQ58125316
Dexpramipexole effects on functional decline and survival in subjects with amyotrophic lateral sclerosis in a Phase II study: Subgroup analysis of demographic and clinical characteristicsQ58125542
P433issue7-8
P921main subjectamyotrophic lateral sclerosisQ206901
P304page(s)519-527
P577publication date2017-08-01
P1433published inAmyotrophic Lateral Sclerosis and Frontotemporal DegenerationQ23928840
P1476titleExploring the diagnosis delay and ALS functional impairment at diagnosis as relevant criteria for clinical trial enrolment
P478volume18