Kailash Bhatia < Kailash P. Bhatia < Kaili M. Stanley

Facettes :

List of bibliographic references indexed by Kailash P. Bhatia

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
000309 (2011)	Omar S. Mian [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni, Allemagne] ; Petra Schwingenschuh [Royaume-Uni, Autriche] ; Kailash P. Bhatia [Royaume-Uni] ; Brian L. Day [Royaume-Uni]	Gait in SWEDDs patients: Comparison with Parkinson's disease patients and healthy controls
000671 (2010)	Annu Aggarwal [Inde] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Monty Silverdale [Royaume-Uni] ; Reema Paudel [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Shrinivas Desai [Inde] ; Mihir Munshi [Inde] ; Darshana Sanghvi [Inde] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Mohit Bhatt [Inde]	Indian‐subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms
000809 (2010)	Petra Schwingenschuh [Royaume-Uni, Autriche] ; Petra Katschnig [Royaume-Uni, Autriche] ; Ronald Saurugg [Autriche] ; Erwin Ott [Autriche] ; Kailash P. Bhatia [Royaume-Uni]	Artistic profession: A potential risk factor for dopamine dysregulation syndrome in Parkinson's disease?
000B29 (2009)	Susanne A. Schneider [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; John Hardy [Royaume-Uni]	Complicated recessive dystonia parkinsonism syndromes
000E69 (2008)	Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Andrew J. Church [Royaume-Uni] ; Davide Martino [Royaume-Uni, Italie] ; Paul M. Candler [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Gavin Giovannoni [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni]	Antineuronal antibodies in Parkinson's disease
001461 (2005)	Naheed L. Khan ; Shushant Jain ; John M. Lynch ; Nicola Pavese ; Patrick Abou-Sleiman ; Janice L. Holton ; Daniel G. Healy ; William P. Gilks ; Mary G. Sweeney ; Milan Ganguly ; Vaneesha Gibbons ; Sonia Gandhi ; Jenny Vaughan ; Louise H. Eunson ; Regina Katzenschlager ; Juliet Gayton ; Graham Lennox ; Tamas Revesz ; David Nicholl [Royaume-Uni] ; Kailash P. Bhatia ; Niall Quinn ; David Brooks ; Andrew Lees (neurologue) [Royaume-Uni] ; Mary B. Davis ; Paola Piccini ; Andrew B. Singleton [États-Unis] ; Nicholas W. Wood	Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

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List of associated KwdEn.i

Nombre de documents	Descripteur
3	Parkinson's disease
2	dystonia
1	ARSAC = Administration of Radioactive Substances Advisory Committee
1	DDS
1	F-dopa PET = 18F-dopa positron emission tomography
1	LOD = logarithm of the odds
1	LRRK2
1	LRRK2 = leucine-rich, repeat kinase 2
1	Lewy bodies
1	MRI
1	NBIA
1	NFTs = neurofibrillary tangles
1	NHNN = National Hospital for Neurology and Neurosurgery
1	Scans without evidence of dopaminergic deficit; SWEDDs; Parkinson's disease; Gait; Walking
1	UPSIT = University of Pennsylvania Smell Identification Test
1	antineuronal ganglia antibodies
1	artists
1	cM = centimorgan
1	creativity
1	dardarin
1	dopamine
1	eye‐of‐the‐tiger sign
1	genetic
1	inflammation
1	neurodegeneration with brain iron accumulation
1	parkinsonism
1	recessive

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