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Genetics / Health / Parkin / Alpha-synuclein / Neurodegeneration / Presenilin / Chromosome 1 / Point mutation / Genetic disorder / Biology / Geriatrics / Medicine


NeuroRx威: The Journal of the American Society for Experimental NeuroTherapeutics Genetics of Parkinson Disease Nathan Pankratz and Tatiana Foroud Department of Medical and Molecular Genetics, Indiana University School
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City

Paris / Philadelphia / Indianapolis / Lincoln / /

Company

Goldman / Oliveira SA / Experimental NeuroTherapeutics Inc. / Johnson AG / Tan LC / Kao / /

Continent

North America / Europe / /

Country

Netherlands / Italy / Iceland / Greece / /

Currency

pence / /

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Facility

University School / /

IndustryTerm

chromosome using modern technology / strict protocol / disease gene product / gene product / appropriate protocols / heavy metal exposure / Metal-triggered structural transformations / /

MedicalCondition

GENETICS OF PARKINSON DISEASE / simple Mendelian disorder / German Parkinson’s disease / common disease / early-onset parkinsonism / dementia / autosomal Parkinson disease / neurodegenerative disease / tremor-dominant parkinsonism / atypical disease / recessive juvenile parkinsonism / autosomal dominant disease / diffuse Lewy body disease / several diseases / Hereditary Lewy-body parkinsonism / mild dystonia / Huntington disease / autosomal recessive juvenile parkinsonism / common neurodegenerative diseases / slow disease / clinically typical tremor-dominant parkinsonism / individuals GENETICS OF PARKINSON DISEASE / Atypical Parkinsonism / onset Parkinson disease / memory loss / late-onset Parkinson’s disease / neurodegenerative disorders / familial Parkinson disease / Genes influencing Parkinson disease / Mitochondrial dysfunction / late-onset idiopathic Parkinson’s disease / autosomal recessive early-onset parkinsonism / S et al. Familial Parkinson disease / parkinsonism / disease / Parkinson disease / common disorders / OF THE GENETICS OF PARKINSON DISEASE / incurable disease / Kondo C. Paralysis agitans / MM et al. PARK6-linked parkinsonism / common neurodegenerative disorder / theories underlying disease / causative role GENETICS OF PARKINSON DISEASE / familial Parkinson’s disease / autosomal recessive parkinsonism / recessive Parkinson’s disease / Parkinson’s disease / Diseases / early-onset Parkinson’s disease / Alzheimer disease / dystonia / typically adult-onset / neurodegenerative disorder / motor dysfunction / multiplex Parkinson disease / dopaminergic dysfunction / autosomal-recessive type juvenile Parkinsonism / disorders / /

MedicalTreatment

counseling / contraception / /

Organization

PANKRATZ AND FOROUD / Tatiana Foroud Department of Medical and Molecular Genetics / American Society for Experimental NeuroTherapeutics / Aasly J. Allelic association / American Society for Experimental NeuroTherapeutics Genetics / Department of Medical and Molecular Genetics / AR AD / Indiana University School of Medicine / /

Person

Arch Neurol / Ann Neurol / Tatiana Foroud / FOROUD TABLE / Takahashi R. An / GENE TESTS FOR PD / Nathan Pankratz / /

Position

Conneallyu PM / Frosch MP / Niznik HB / Hunter / The specialist neurologist / treating physician / genetic counselor / /

Product

PS2 / /

ProvinceOrState

Indiana / /

RadioStation

Bonnet AM / Lazzarini AM / /

Region

southern Greece / southern Italy / /

Technology

alpha / diagnostic tests / polymerization / cloning / strict protocol / apoptosis / /

SocialTag