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Serveur d'exploration sur la maladie de Parkinson - Corpus (Accueil)

Index « Auteurs » - entrée « John Hardy »
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John Hardman < John Hardy < John J. Gallagher  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 19.
Ident.Authors (with country if any)Title
000228 (2011) Michael J. Devine ; Katrina Gwinn ; Andrew Singleton ; John HardyParkinson's disease and α‐synuclein expression
000588 (2009) Sarah Teixeira Camargos ; Leonardo Oliveira Dornas ; Parastoo Momeni ; Andrew Lees ; John Hardy ; Andrew Singleton ; Francisco CardosoFamilial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations
000619 (2012) Jose Bras ; Rita Guerreiro ; John HardyUse of next-generation sequencing and other whole-genome strategies to dissect neurological disease
000623 (2009) Juliane Neumann ; Jose Bras ; Emma Deas ; Sean S. O'Sullivan ; Laura Parkkinen ; Robin H. Lachmann ; Abi Li ; Janice Holton ; Rita Guerreiro ; Reema Paudel ; Badmavady Segarane ; Andrew Singleton ; Andrew Lees ; John Hardy ; Henry Houlden ; Tamas Revesz ; Nicholas W. WoodGlucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
000765 (2005) Aideen Mcinerney-Leo ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John HardyGenetic testing in Parkinson's disease
000A62 (2002) Andrew West ; Magali Periquet ; Sarah Lincoln ; Christoph B. Lücking ; David Nicholl ; Vincenzo Bonifati ; Nina Rawal ; Thomas Gasser ; Ebba Lohmann ; Jean-François Deleuze ; Demetrius Maraganore ; Allan Levey ; Nick Wood ; Alexandra Dürr ; John Hardy ; Alexis Brice ; Matt FarrerComplex relationship between Parkin mutations and Parkinson disease
000A85 (2011) Thomas Gasser ; John Hardy ; Yoshikuni MizunoMilestones in PD genetics
001160 (2009) Susanne A. Schneider ; Kailash P. Bhatia ; John HardyComplicated recessive dystonia parkinsonism syndromes
001571 (1999) Matt Farrer ; Katrina Gwinn-Hardy ; Mike Hutton ; John HardyThe Genetics of Disorders with Synuclein Pathology and Parkinsonism
001D61 (2006) John Hardy ; Huaiban Cai ; Mark R. Cookson ; Katrina Gwinn-Hardy ; Andrew SingletonGenetics of Parkinson's disease and parkinsonism
002008 (2001) Matt Farrer ; Piu Chan ; Rong Chen ; Louis Tan ; Sarah Lincoln ; Dena Hernandez ; Lysia Forno ; Katrina Gwinn-Hardy ; Leonard Petrucelli ; Jennifer Hussey ; Andrew Singleton ; Caroline Tanner ; John Hardy ; J. William LangstonLewy bodies and parkinsonism in families with parkin mutations
002179 (2005) Jordi Clarimon ; Janel Johnson ; Okan Dogu ; Wagner Horta ; Naheed Khan ; Andrew J. Lees ; John Hardy ; Andrew SingletonDefining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease
002290 (2004) Joseph Wiley ; Timothy Lynch ; Sarah Lincoln ; Lisa Skipper ; Mary Hulihan ; David Gosal ; Gina Bisceglio ; Jennifer Kachergus ; John Hardy ; Matthew J. FarrerParkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations
002348 (2004) Amanda Singleton ; Katrina Gwinn-Hardy ; Yehonotan Sharabi ; Sheng-Ting Li ; Courtney Holmes ; Raghuveer Dendi ; John Hardy ; Andrew Singleton ; Anthony Crawley ; David S. GoldsteinAssociation between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication
002514 (2008) Javier Simon-Sanchez ; Sonja Scholz ; Maria Del Mar Matarin ; Hon-Chung Fung ; Dena Hernandez ; J Raphael Gibbs ; Angela Britton ; John Hardy ; Andrew SingletonGenomewide SNP assay reveals mutations underlying Parkinson disease
002798 (1999) John HardyPathways to Primary Neurodegenerative Disease
002A18 (1995) John HardyApolipoprotein E in the genetics and epidemiology of Alzheimer's disease
002C64 (1999) Matt Farrer ; Katrina Gwinn-Hardy ; Manfred Muenter ; Fabienne Wavrant Devrieze ; Richard Crook ; Jordi Perez-Tur ; Sarah Lincoln ; Demetrius Maraganore ; Charles Adler ; Stephanie Newman ; Kari Macelwee ; Page Mccarthy ; Carol Miller ; Cheryl Waters ; John HardyA Chromosome 4P Haplotype Segregating with Parkinson's Disease and Postural Tremor
002C98 (2010) Annu Aggarwal ; Susanne A. Schneider ; Henry Houlden ; Monty Silverdale ; Reema Paudel ; Coro Paisan-Ruiz ; Shrinivas Desai ; Mihir Munshi ; Darshana Sanghvi ; John Hardy ; Kailash P. Bhatia ; Mohit BhattIndian‐subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms

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