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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2009-12-16
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pubmed:abstractText |
To determine the motor phenotype of LRRK2 G2019S mutation carriers. LRRK2 mutation carriers were previously reported to manifest the tremor dominant motor phenotype, which has been associated with slower motor progression and less cognitive impairment compared with the postural instability and gait difficulty (PIGD) phenotype.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1538-3687
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pubmed:author |
pubmed-author:AlcalayRoy NRN,
pubmed-author:AndrewsHoward FHF,
pubmed-author:BressmanSusanS,
pubmed-author:CaccappoloEliseE,
pubmed-author:ClarkLorraine NLN,
pubmed-author:ColcherAmyA,
pubmed-author:ComellaCynthia LCL,
pubmed-author:CoteLucien JLJ,
pubmed-author:FahnStanleyS,
pubmed-author:FordBlairB,
pubmed-author:FriedmanJoseph HJH,
pubmed-author:FruchtSteven JSJ,
pubmed-author:HinerBradleyB,
pubmed-author:JenningsDannaD,
pubmed-author:KisselevSergeyS,
pubmed-author:LouisElan DED,
pubmed-author:MarderKaren SKS,
pubmed-author:MarshLauraL,
pubmed-author:Mejia-SantanaHelenH,
pubmed-author:MickelSusan FSF,
pubmed-author:NanceMartha AMA,
pubmed-author:NovakKevinK,
pubmed-author:OttmanRuthR,
pubmed-author:PfeifferRonaldR,
pubmed-author:RezakMichaelM,
pubmed-author:RosadoLlencyL,
pubmed-author:RossBarbara MBM,
pubmed-author:ScottWilliam KWK,
pubmed-author:SiderowfAndrewA,
pubmed-author:TangMing XinMX,
pubmed-author:TannerCarolineC,
pubmed-author:VerbitskyMiguelM,
pubmed-author:WatersCheryl HCH
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pubmed:issnType |
Electronic
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1517-22
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pubmed:dateRevised |
2011-9-26
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pubmed:meshHeading |
pubmed-meshheading:20008657-Adult,
pubmed-meshheading:20008657-Age of Onset,
pubmed-meshheading:20008657-Cross-Sectional Studies,
pubmed-meshheading:20008657-Female,
pubmed-meshheading:20008657-Genetic Variation,
pubmed-meshheading:20008657-Heterozygote,
pubmed-meshheading:20008657-Humans,
pubmed-meshheading:20008657-Male,
pubmed-meshheading:20008657-Middle Aged,
pubmed-meshheading:20008657-Motor Skills Disorders,
pubmed-meshheading:20008657-Parkinson Disease,
pubmed-meshheading:20008657-Phenotype,
pubmed-meshheading:20008657-Protein-Serine-Threonine Kinases
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pubmed:year |
2009
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pubmed:articleTitle |
Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease.
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pubmed:affiliation |
Department of Neurology, Columbia University, New York, NY 10032, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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