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

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]

Ident.	Authors (with country if any)	Title
000801 (2002)	Jason D. Warren [Royaume-Uni] ; Catherine J. Mummery ; Amir S. Al-Din ; Peter Brown ; Nicholas W. Wood	Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike?
000831 (2002)	Sian D. Spacey [Royaume-Uni] ; Enza-Maria Valente ; Gurusidheshwar M. Wali ; Thomas T. Warner ; Paul R. Jarman ; Anthony H V. Schapira ; Peter H. Dixon ; Mary B. Davis ; Kailash P. Bhatia ; Nicholas W. Wood	Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
000A03 (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?
001131 (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.
001289 (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).
001324 (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.
001468 (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.
001828 (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.
001845 (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.
002300 (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.
002589 (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.
002846 (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.
002C57 (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.
002C86 (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.
002F60 (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.
003574 (2012)	Alisdair Mcneill [Royaume-Uni] ; Raquel Duran [Royaume-Uni] ; Christos Proukakis [Royaume-Uni] ; Jose Bras [Royaume-Uni] ; Derralyn Hughes [Royaume-Uni] ; Atuhl Mehta [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Anthony H. V. Schapira [Royaume-Uni]	Hyposmia and Cognitive Impairment in Gaucher Disease Patients and Carriers
003791 (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.
003919 (2012)	Maja Kojovic [Royaume-Uni] ; Una-Marie Sheerin [Royaume-Uni] ; Ignacio Rubio-Agusti [Royaume-Uni] ; Anirban Saha ; Jose Bras [Royaume-Uni] ; Vaneesha Gibbons [Royaume-Uni] ; Rodger Palmer [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family
003921 (2012)	Raquel Duran [Royaume-Uni] ; Niccolo E. Mencacci [Royaume-Uni, Italie] ; Aikaterini V. Angeli [Royaume-Uni] ; Maryam Shoai [Royaume-Uni] ; Emma Deas [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Atul Mehta [Royaume-Uni] ; Derralynn Hughes [Royaume-Uni] ; Timothy M. Cox [Royaume-Uni] ; Patrick Deegan [Royaume-Uni] ; Anthony H. Schapira [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Patricia Limousin [Royaume-Uni] ; Paul R. Jarman [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Tom Foltynie [Royaume-Uni]	The Glucocerobrosidase E326K Variant Predisposes to Parkinson’s Disease, But Does Not Cause Gaucher’s Disease
003964 (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.
003C26 (2013)	Aikaterina Angeli [Royaume-Uni] ; Niccolo E. Mencacci [Royaume-Uni, Italie] ; Raquel Duran [Royaume-Uni] ; Iciar Aviles-Olmos [Royaume-Uni] ; Zinovia Kefalopoulou [Royaume-Uni] ; Joseph Candelario [Royaume-Uni] ; Sarah Rusbridge [Royaume-Uni] ; Jennifer Foley [Royaume-Uni] ; Priyanka Pradhan [Royaume-Uni] ; Marjan Jahanshahi [Royaume-Uni] ; Ludvic Zrinzo [Royaume-Uni] ; Marwan Hariz [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; John Hardy [Royaume-Uni] ; Patricia Limousin [Royaume-Uni] ; Tom Foltynie [Royaume-Uni]	Genotype and phenotype in Parkinson's disease: Lessons in heterogeneity from deep brain stimulation

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