John Hardman < John Hardy < John Hiu-Ming Chan

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 45.
[0-20] [0 - 20][0 - 45][20-40]

Ident.	Authors (with country if any)	Title
000172 (2015)	Alastair J. Noyce ; Niccolo E. Mencacci ; Anette Schrag ; Jonathan P. Bestwick [Royaume-Uni] ; Gavin Giovannoni [Royaume-Uni] ; Andrew J. Lees ; John Hardy	Web-based assessment of Parkinson's prodromal markers identifies GBA variants.
000293 (2015)	Björn Br Ndl [Allemagne] ; Susanne A. Schneider ; Jeanne F. Loring ; John Hardy ; Philip Gribbon ; Franz-Josef Müller	Stem cell reprogramming: basic implications and future perspective for movement disorders.
000301 (2015)	Roberto Erro [Royaume-Uni] ; Joshua Hersheson [Royaume-Uni] ; Christos Ganos [Royaume-Uni] ; Niccol E. Mencacci [Royaume-Uni] ; Maria Stamelou [Royaume-Uni] ; Amit Batla [Royaume-Uni] ; Stefanie Catherine Thust [Royaume-Uni] ; Jose M. Bras [Royaume-Uni] ; Rita J. Guerreiro [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?
000553 (2014)	Daniela Berg [Allemagne] ; Ronald B. Postuma ; Bastiaan Bloem ; Piu Chan ; Bruno Dubois ; Thomas Gasser ; Christopher G. Goetz ; Glenda M. Halliday ; John Hardy ; Anthony E. Lang ; Irene Litvan ; Kenneth Marek ; José Obeso ; Wolfgang Oertel ; C Warren Olanow ; Werner Poewe ; Matthew Stern ; Günther Deuschl	Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease.
000679 (2014)	Kin Y. Mok [Royaume-Uni] ; Susanne A. Schneider ; Daniah Trabzuni ; Maria Stamelou ; Mark Edwards ; Dalia Kasperaviciute ; Stuart Pickering-Brown ; Monty Silverdale ; John Hardy ; Kailash P. Bhatia	Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.
000856 (2013)	Aikaterina Angeli [Royaume-Uni] ; Niccolo E. Mencacci ; Raquel Duran ; Iciar Aviles-Olmos ; Zinovia Kefalopoulou ; Joseph Candelario ; Sarah Rusbridge ; Jennifer Foley ; Priyanka Pradhan ; Marjan Jahanshahi ; Ludvic Zrinzo ; Marwan Hariz ; Nicholas W. Wood ; John Hardy ; Patricia Limousin ; Tom Foltynie	Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation.
000917 (2013)	Karen M. Doherty [Royaume-Uni] ; John Hardy	Parkin disease and the Lewy body conundrum.
000A06 (2013)	John Hardy	Reply to Letter: Identical twins with leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
000B17 (2012)	Maja Kojovic ; Una-Marie Sheerin ; Ignacio Rubio-Agusti ; Anirban Saha ; Jose Bras ; Vaneesha Gibbons ; Rodger Palmer ; Henry Houlden ; John Hardy ; Nicholas W. Wood ; Kailash P. Bhatia	Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
000B42 (2013)	Raquel Duran [Royaume-Uni] ; Niccolo E. Mencacci ; Aikaterini V. Angeli ; Maryam Shoai ; Emma Deas ; Henry Houlden ; Atul Mehta ; Derralynn Hughes ; Timothy M. Cox ; Patrick Deegan ; Anthony H. Schapira ; Andrew J. Lees ; Patricia Limousin ; Paul R. Jarman ; Kailash P. Bhatia ; Nicholas W. Wood ; John Hardy ; Tom Foltynie	The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
000C76 (2012)	Georgia Xiromerisiou [Grèce] ; Henry Houlden ; Nikolaos Scarmeas ; Maria Stamelou ; Eleanna Kara ; John Hardy ; Andrew J. Lees ; Prasad Korlipara ; Patricia Limousin ; Reema Paudel ; Georgios M. Hadjigeorgiou ; Kailash P. Bhatia	THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.
000E17 (2012)	Georgia Xiromerisiou ; Henry Houlden ; Anna Sailer ; Laura Silveira-Moriyama ; John Hardy ; Andrew J. Lees	Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
000E56 (2012)	Alisdair Mcneill [Royaume-Uni] ; Raquel Duran ; Christos Proukakis ; Jose Bras ; Derralyn Hughes ; Atuhl Mehta ; John Hardy ; Nicholas W. Wood ; Anthony H V. Schapira	Hyposmia and cognitive impairment in Gaucher disease patients and carriers.
000F18 (2012)	Núria Set Salvia [Espagne] ; Javier Pagonabarraga ; Henry Houlden ; Berta Pascual-Sedano ; Oriol Dols-Icardo ; Arianna Tucci ; Coro Paisán-Ruiz ; Antonia Campolongo ; Sofía Ant N-Aguirre ; Inés Martín ; Laia Mu Oz ; Enric Bufill ; Lluïsa Vilageliu ; Daniel Grinberg ; M Nica Cozar ; Rafael Blesa ; Alberto Lle ; John Hardy ; Jaime Kulisevsky ; Jordi Clarim N	Glucocerebrosidase mutations confer a greater risk of dementia during Parkinson's disease course.
000F83 (2012)	Susanne A. Schneider [Allemagne] ; John Hardy ; Kailash P. Bhatia	Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations.
001060 (2011)	Michael J. Devine [Royaume-Uni] ; Katrina Gwinn ; Andrew Singleton ; John Hardy	Parkinson's disease and α-synuclein expression.
001143 (2011)	Katrina Gwinn ; Michael J. Devine ; Lee-Way Jin ; Janel Johnson ; Thomas Bird ; Manfred Muenter ; Cheryl Waters ; Charles H. Adler ; Richard Caselli ; Henry Houlden ; Grisel Lopez ; Amanda Singleton ; John Hardy ; Andrew Singleton	Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α-synuclein triplication (Iowa kindred).
001173 (2011)	Thomas Gasser [Allemagne] ; John Hardy ; Yoshikuni Mizuno	Milestones in PD genetics.
001652 (2010)	Coro Paisán-Ruiz [Royaume-Uni] ; Rocio Guevara ; Monica Federoff ; Hasmet Hanagasi ; Fardaz Sina ; Elahe Elahi ; Susanne A. Schneider ; Petra Schwingenschuh ; Nin Bajaj ; Murat Emre ; Andrew B. Singleton ; John Hardy ; Kailash P. Bhatia ; Sebastian Brandner ; Andrew J. Lees ; Henry Houlden	Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
001735 (2010)	Annu Aggarwal [Inde] ; Susanne A. Schneider ; Henry Houlden ; Monty Silverdale ; Reema Paudel ; Coro Paisan-Ruiz ; Shrinivas Desai ; Mihir Munshi ; Darshana Sanghvi ; John Hardy ; Kailash P. Bhatia ; Mohit Bhatt	Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.
001882 (2010)	Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz ; Niall P. Quinn ; Andrew J. Lees ; Henry Houlden ; John Hardy ; Kailash P. Bhatia	ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.

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