About: John G Nutt

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

American researcher

Attributes	Values
rdf:type	Item
description	Forscher (de) investigador (es) chercheur (fr) дослідник (uk) 研究者 (zh) 研究員 (ja) onderzoeker (nl) American researcher (en) باحث أمريكي (ar)
rdfs:label	John G Nutt (en) John G Nutt (es) John G Nutt (nl) John G Nutt (ast)
skos:prefLabel	John G Nutt (en) John G Nutt (es) John G Nutt (nl) John G Nutt (ast)
name	John G Nutt (en) John G Nutt (es) John G Nutt (nl) John G Nutt (ast)
given name	wds:Q67175555-8D6DAE27-AA73-4D89-B750-73CF4C4758B2
given name	John
instance of	wds:Q67175555-A1CD6FCF-B8AE-4B2F-B73A-17589BCB52AC
instance of	Homo sapiens
skos:altLabel	John Nutt (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q67175555-fa2468d5-8a66-46c2-8cc0-b8c6842d618b
employer	wds:Q67175555-206CE488-083C-4B95-88CC-310A5B11A739
sex or gender	wds:Q67175555-797A4427-EE5E-4C49-817E-7A4A5FB5538D
VIAF ID	wds:Q67175555-447A0D42-C8AE-4714-865B-260930D97271
IdRef ID	wds:Q67175555-0b9be9d3-d084-45e1-b258-d31b51969608
educated at	wds:Q67175555-E74A03FE-8677-49B0-A625-5E919EE955DE
family name	wds:Q67175555-8DD483D2-8705-45E6-9A86-5B4E03BD344F
WorldCat Identities ID (superseded)	wds:Q67175555-87909760-E7DD-491F-B591-D53FFB5D41D7
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p110444361
VIAF ID	http://viaf.org/viaf/51763792
IdRef ID	http://www.idref.fr/085859338/id
Nationale Thesaurus voor Auteursnamen ID	110444361
employer	Oregon Health & Science University
sex or gender	male
VIAF ID	51763792
IdRef ID	085859338
educated at	Rice University
family name	Nutt
WorldCat Identities ID (superseded)	lccn-n92803532
ORCID iD	wds:Q67175555-D39C100E-64C1-4FD8-9983-294357FDF703
ORCID iD	https://orcid.org/0000-0003-2759-1106
ORCID iD	0000-0003-2759-1106
is owl:sameAs of	John G Nutt
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67175555
is author of	Effects of a central cholinesterase inhibitor on reducing falls in Parkinson disease Randomized controlled trial of intraputamenal glial cell line-derived neurotrophic factor infusion in Parkinson disease Testing objective measures of motor impairment in early Parkinson's disease: Feasibility study of an at-home testing device Clinical practice. Diagnosis and initial management of Parkinson's disease Reduced performance in balance, walking and turning tasks is associated with increased neck tone in Parkinson's disease Postural muscle tone in the body axis of healthy humans. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk. Postural muscle responses to multidirectional translations in patients with Parkinson's disease Abnormal force patterns for multidirectional postural responses in patients with Parkinson's disease Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease Exploring gene-environment interactions in Parkinson’s disease A randomized controlled trial of etilevodopa in patients with Parkinson disease who have motor fluctuations. Strategies to advance translational research into brain barriers Multicenter, open-label, trial of sarizotan in Parkinson disease patients with levodopa-induced dyskinesias (the SPLENDID Study). Direction-specific postural instability in subjects with Parkinson's disease Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee Functional reorganization of the locomotor network in Parkinson patients with freezing of gait Pharmacokinetic and pharmacodynamic changes during the first four years of levodopa treatment in Parkinson's disease Dyskinesia and the antiparkinsonian response always temporally coincide: a retrospective study The dopamine transporter: importance in Parkinson's disease Evolution of the response to levodopa during the first 4 years of therapy. Disease progression, drug action and Parkinson's disease: why time cannot be ignored Parkinson's disease Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease Treatment of Parkinson's disease with trophic factors iTUG, a sensitive and reliable measure of mobility The instrumented timed up and go test: potential outcome measure for disease modifying therapies in Parkinson's disease Trunk accelerometry reveals postural instability in untreated Parkinson's disease Gene delivery of AAV2-neurturin for Parkinson's disease: a double-blind, randomised, controlled trial Modeling the short- and long-duration responses to exogenous levodopa and to endogenous levodopa production in Parkinson's disease A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit CSF multianalyte profile distinguishes Alzheimer and Parkinson diseases Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations Analyzing 180 degrees turns using an inertial system reveals early signs of progression of Parkinson's disease. Importance of within subject variation in levodopa pharmacokinetics: a 4 year cohort study in Parkinson's disease Preferences of patients with Parkinson's disease for communication about advanced care planning Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease Knee trembling during freezing of gait represents multiple anticipatory postural adjustments Quantifying freezing of gait in Parkinson's disease during the instrumented timed up and go test Postural sway as a marker of progression in Parkinson's disease: a pilot longitudinal study Higher-level gait disorders: an open frontier Milestones in gait, balance, and falling. Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2). Cognitive and motor function in long-duration PARKIN-associated Parkinson disease Using modafinil to treat fatigue in Parkinson disease: a double-blind, placebo-controlled pilot study. Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

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