Nicholas W. Sterling < Nicholas W. Wood < Nicholas Wood

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List of bibliographic references

Number of relevant bibliographic references: 23.
[0-20] [0 - 20][0 - 23][20-22][20-40]

Ident.	Authors (with country if any)	Title
000541 (2014)	Christos Proukakis [Royaume-Uni] ; Maryiam Shoaee ; James Morris ; Timothy Brier ; Eleanna Kara ; Una-Marie Sheerin ; Gavin Charlesworth ; Eduardo Tolosa ; Henry Houlden ; Nicholas W. Wood ; Anthony H. Schapira	Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.
000606 (2014)	Maria Stamelou [Grèce] ; Gavin Charlesworth ; Carla Cordivari ; Susanne A. Schneider ; Georg K Gi ; Una-Marie Sheerin ; Ignacio Rubio-Agusti ; Amit Batla ; Henry Houlden ; Nicholas W. Wood ; Kailash P. Bhatia	The phenotypic spectrum of DYT24 due to ANO3 mutations.
000681 (2014)	Gavin Charlesworth [Royaume-Uni] ; Kailash P. Bhatia ; Nicholas W. Wood	No pathogenic GNAL mutations in 192 sporadic and familial cases of cervical dystonia.
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.
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.
000C55 (2012)	Laura L. Kilarski [Royaume-Uni] ; Justin P. Pearson ; Victoria Newsway ; Elisa Majounie ; M Duleeka W. Knipe ; Anjum Misbahuddin ; Patrick F. Chinnery ; David J. Burn ; Carl E. Clarke ; Marie-Helene Marion ; Alistair J. Lewthwaite ; David J. Nicholl ; Nicholas W. Wood ; Karen E. Morrison ; Caroline H. Williams-Gray ; Jonathan R. Evans ; Stephen J. Sawcer ; Roger A. Barker ; Mirdhu M. Wickremaratchi ; Yoav Ben-Shlomo ; Nigel M. Williams ; Huw R. Morris	Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset 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.
001460 (2011)	Helen Ling [Royaume-Uni] ; James M. Polke ; Mary G. Sweeney ; Andrea Haworth ; Catherine A. Sandford ; Simon J R. Heales ; Nicholas W. Wood ; Mary B. Davis ; Andrew J. Lees	An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia family.
001731 (2010)	Araceli Alonso-Canovas ; Petra Katschnig ; Arianna Tucci ; Miryam Carecchio ; Nicholas W. Wood ; Mark Edwards ; Juan Carlos Martínez Castrillo ; Derek Burke ; Simon Heales ; Kailash P. Bhatia	Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: case report and literature review.
001760 (2010)	Georg K Gi [Royaume-Uni] ; Christine Klein ; Nicholas W. Wood ; Susanne A. Schneider ; Peter P. Pramstaller ; Vera Tadic ; Niall P. Quinn ; Bart P C. Van De Warrenburg ; Kailash P. Bhatia	Nonmotor symptoms in Parkin gene-related parkinsonism.
001B37 (2009)	Nicola Pavese [Royaume-Uni] ; Naheed L. Khan ; Christoph Scherfler ; Lisa Cohen ; David J. Brooks ; Nicholas W. Wood ; Kailash P. Bhatia ; Niall P. Quinn ; Andrew J. Lees ; Paola Piccini	Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: an 18F-dopa PET progression study.
001D88 (2009)	Daniel G. Healy ; Susan Bressman ; John Dickson ; Laura Silveira-Moriyama ; Susanne A. Schneider ; Sean S O. Sullivan ; Luke Massey ; Kailash P. Bhatia ; Karen Shaw ; Kailash P. Bhatia ; Jamshed Bomanji ; Nicholas W. Wood ; Andrew J. Lees	Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndrome.
002063 (2008)	Susanne A. Schneider [Royaume-Uni] ; Penelope Talelli ; Binith J. Cheeran ; Naheed L. Khan ; Nicholas W. Wood ; John C. Rothwell ; Kailash P. Bhatia	Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations.
002A94 (2006)	Daniel G. Healy [Royaume-Uni] ; Patrick M. Abou-Sleiman ; Kourosh R. Ahmadi ; Sonia Gandhi ; Miratul M. Muqit ; Kailash P. Bhatia ; Niall P. Quinn ; Andrew J. Lees ; Janice L. Holton ; Tamas Revesz ; Nicholas W. Wood	NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.
002B11 (2006)	Ina Schmitt ; Ullrich Wüllner ; Daniel G. Healy ; Nicholas W. Wood ; Heike Kölsch ; Reinhard Heun	The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
002E60 (2006)	Michele T M. Hu [Royaume-Uni] ; Christoph Scherfler ; Naheed L. Khan ; Jo V. Hajnal ; Andrew J. Lees ; Niall Quinn ; Nicholas W. Wood ; David J. Brooks	Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease.
002F88 (2005)	Daniel G. Healy ; Patrick M. Abou-Sleiman ; Niall Quinn ; Kourosh R. Ahmadi ; Tetsutaro Ozawa ; Christoph Kamm ; Ullrich Wullner ; Wolfgang H. Oertel ; Katrin Burk ; Erik Dupont ; Maria T. Pellecchia ; Eduardo Tolosa ; Thomas Gasser ; Janice L. Holton ; Tamas Revesz ; David B. Goldstein ; Andrew J. Lees ; Nicholas W. Wood	UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.
003023 (2005)	Naheed L. Khan [Royaume-Uni] ; Paola Giunti ; Mary G. Sweeney ; Christoph Scherfler ; Michael O. Brien ; Paola Piccini ; Nicholas W. Wood ; Andrew J. Lees	Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).
003170 (2005)	Naheed L. Khan [Royaume-Uni] ; Wagner Horta ; Louise Eunson ; Elizabeth Graham ; Janel O. Johnson ; Shannon Chang ; Mary Davis ; Andrew Singleton ; Nicholas W. Wood ; Andrew J. Lees	Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years.
003848 (2003)	Mikko Kuoppam Ki [Royaume-Uni] ; Paula Giunti ; Niall Quinn ; Nicholas W. Wood ; Kailash P. Bhatia	Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?

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