John Hardman < John Hardy < John Hiu-Ming Chan

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 46.
[0-20] [0 - 20][0 - 46][20-40]

Ident.	Authors (with country if any)	Title
000679 (2002)	Virgilio Gerald H. Evidente [États-Unis] ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew Singleton	X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?
000825 (2002)	Ruey-Meei Wu [République populaire de Chine] ; Din-E Shan ; Chen-Ming Sun ; Ren-Shyan Liu ; Wuh-Liang Hwu ; Chun-Hwei Tai ; Jennifer Hussey ; Andrew West ; Katrina Gwinn-Hardy ; John Hardy ; Judy Chen ; Matt Farrer ; Sarah Lincoln	Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.
000911 (2002)	S H Subramony [États-Unis] ; Dena Hernandez ; Amanda Adam ; Stephanie Smith-Jefferson ; Jennifer Hussey ; Katrina Gwinn-Hardy ; Timothy Lynch ; Olga Mcdaniel ; John Hardy ; Matt Farrer ; Andrew Singleton	Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians.
000939 (2002)	Virgilio Gerald H. Evidente [États-Unis] ; Joel Advincula ; Raymund Esteban ; Paul Pasco ; Jhoe Anthony Alfon ; Filipinas F. Natividad ; Joven Cuanang ; Amado San Luis ; Katrina Gwinn-Hardy ; John Hardy ; Dena Hernandez ; Andrew Singleton	Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.
000A41 (2003)	Haydeh Payami [États-Unis] ; John Nutt ; Steven Gancher ; Thomas Bird ; Melissa Gonzales Mcneal ; William K. Seltzer ; Jennifer Hussey ; Paul Lockhart ; Katrina Gwinn-Hardy ; Amanda A. Singleton ; Andrew B. Singleton ; John Hardy ; Matthew Farrer	SCA2 may present as levodopa-responsive parkinsonism.
000A95 (2003)	Louis C. Tan [États-Unis] ; Caroline M. Tanner ; Rong Chen ; Piu Chan ; Matthew Farrer ; John Hardy ; J William Langston	Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation.
000B58 (2003)	John Hardy [États-Unis]	Impact of genetic analysis on Parkinson's disease research.
000E36 (2004)	Sarah Furtado [Canada] ; Haydeh Payami ; Paul J. Lockhart ; Melissa Hanson ; John G. Nutt ; Andrew A. Singleton ; Amanda Singleton ; Jamel Bower ; Ryan J. Utti ; Thomas D. Bird ; Raul De La Fuente-Fernandez ; Yoshio Tsuboi ; Mary L. Klimek ; Oksana Suchowersky ; John Hardy ; Donald B. Calne ; Zbigniew K. Wszolek ; Matthew Farrer ; Katrina Gwinn-Hardy ; A Jon Stoessl	Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
000E44 (2004)	Joseph Wiley [Irlande (pays)] ; Timothy Lynch ; Sarah Lincoln ; Lisa Skipper ; Mary Hulihan ; David Gosal ; Gina Bisceglio ; Jennifer Kachergus ; John Hardy ; Matthew J. Farrer	Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations.
000E69 (2004)	Lorraine N. Clark [États-Unis] ; Shehla Afridi ; Helen Mejia-Santana ; Juliette Harris ; Elan D. Louis ; Lucien J. Cote ; Howard Andrews ; Andrew Singleton ; Fabienne Wavrant De-Vrieze ; John Hardy ; Richard Mayeux ; Stanley Fahn ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Ruth Ottman ; Karen Marder	Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
000E72 (2004)	Okan Dogu [Turquie] ; Janel Johnson ; Dena Hernandez ; Melissa Hanson ; John Hardy ; Hulya Apaydin ; Sibel Ozekmekçi ; Serhan Sevim ; Katrina Gwinn-Hardy ; Andrew Singleton	A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.
001075 (2005)	Aideen Mcinerney-Leo [États-Unis] ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John Hardy	Genetic testing in Parkinson's disease.
001355 (2005)	Parastoo Momeni [États-Unis] ; Chin-Song Lu ; Yah-Huei Wu Chou ; Hsiu-Chen Chang ; Rou-Shayn Chen ; Chiung-Chu Chen ; Jin-Tian Hsu ; Andrew Singleton ; John Hardy	Taiwanese cases of SCA2 are derived from a single founder.
001369 (2005)	John Hardy [États-Unis] ; Andrew J. Lees	Parkinson's disease: a broken nosology.
001428 (2005)	Jose Miguel Bras [Portugal] ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew Singleton	G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.
001581 (2006)	Hon-Chung Fung [États-Unis] ; Chiung-Mei Chen ; John Hardy ; Dena Hernandez ; Andrew Singleton ; Yih-Ru Wu	Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease.
001621 (2006)	Liana Fidani [Grèce] ; Kallirhoe Kalinderi ; Sevasti Bostantjopoulou ; Jordi Clarimon ; Antonis Goulas ; Zoe Katsarou ; John Hardy ; Alexandros Kotsis	Association of the Tau haplotype with Parkinson's disease in the Greek population.
001809 (2006)	John Hardy	No definitive evidence for a role for the environment in the etiology of Parkinson's disease.
001F37 (2008)	Sarah Teixeira Camargos [Brésil] ; Francisco Cardoso ; Parastoo Momeni ; Juliana Gurgel Gianetti ; Andrew Lees ; John Hardy ; Andrew Singleton	Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
002138 (2008)	Rita Joao Guerreiro [États-Unis] ; Isabel Santana ; Jose Miguel Bras ; Tamas Revesz ; Olinda Rebelo ; Maria Helena Ribeiro ; Beatriz Santiago ; Catarina Resende Oliveira ; Andrew Singleton ; John Hardy	Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS cases.
002381 (2009)	Mindhu M. Wickremaratchi ; Elisa Majounie ; Huw R. Morris ; Nigel M. Williams ; Helen Lewis ; Steven S. Gill ; Sadaquate Khan ; Peter Heywood ; John Hardy ; Charles M. Wiles ; Andrew B. Singleton ; Niall P. Quinn	Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome.

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