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Neurology
|
October 1, 1990
Dystonia in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy
J Rivest, N Quinn, C D Marsden
Neurology
|
June 1, 1981
Bromocriptine and domperidone in the treatment of Parkinson disease
N Quinn, A Illas, F Lhermitte, et al.
Neurology
|
September 1, 1984
Control of on/off phenomenon by continuous intravenous infusion of levodopa
N Quinn, J D Parkes, C D Marsden
Neurology
|
July 9, 2003
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
H R Morris, Y Osaki, J Holton, et al.
Neurology
|
April 14, 2004
Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease
N L Khan, R Katzenschlager, H Watt, et al.
Neurology
|
November 29, 2002
Do published criteria improve clinical diagnostic accuracy in multiple system atrophy?
Y Osaki, G K Wenning, S E Daniel, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Neurology
|
July 13, 2006
Measuring quality of life in PSP: the PSP-QoL
A Schrag, C Selai, N Quinn, et al.
Neurology
|
September 27, 2006
Severe tongue protrusion dystonia: clinical syndromes and possible treatment
S A Schneider, A Aggarwal, M Bhatt, et al.
Neurology
|
January 12, 2005
Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation
N L Khan, C Scherfler, E Graham, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Neurology
|
October 1, 1990
Dystonia in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy
J Rivest, N Quinn, C D Marsden
Neurology
|
June 1, 1981
Bromocriptine and domperidone in the treatment of Parkinson disease
N Quinn, A Illas, F Lhermitte, et al.
Neurology
|
September 1, 1984
Control of on/off phenomenon by continuous intravenous infusion of levodopa
N Quinn, J D Parkes, C D Marsden
Neurology
|
July 9, 2003
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
H R Morris, Y Osaki, J Holton, et al.
Neurology
|
April 14, 2004
Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease
N L Khan, R Katzenschlager, H Watt, et al.
Neurology
|
November 29, 2002
Do published criteria improve clinical diagnostic accuracy in multiple system atrophy?
Y Osaki, G K Wenning, S E Daniel, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Neurology
|
July 13, 2006
Measuring quality of life in PSP: the PSP-QoL
A Schrag, C Selai, N Quinn, et al.
Neurology
|
September 27, 2006
Severe tongue protrusion dystonia: clinical syndromes and possible treatment
S A Schneider, A Aggarwal, M Bhatt, et al.
Neurology
|
January 12, 2005
Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation
N L Khan, C Scherfler, E Graham, et al.
Page
of 2