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Canadian Medical Association Journal
|
March 24, 2010
LEAKAGE OF CEREBROSPINAL FLUID THROUGH THE CRIBRIFORM PLATE OF THE ETHMOID BONE
A B Singleton
Neurology
|
August 20, 2008
Yet another spinocerebellar ataxia: the saga continues
O Bandmann, A B Singleton
Clinical Genetics
|
June 10, 2011
Exome sequencing in Parkinson's disease
Jose M Bras, A B Singleton
Neuroscience Letters
|
September 12, 2006
PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease
M M Matarin, A B Singleton, H Houlden
Cell and Tissue Research
|
March 15, 2018
Genetic risk factors in Parkinson's disease
K J Billingsley, S Bandres-Ciga, S Saez-Atienzar, et al.
European Journal of Neurology
|
March 16, 2013
Mutations in EIF4G1 are not a common cause of Parkinson's disease
A Siitonen, E Majounie, M Federoff, et al.
Lancet (London, England)
|
July 31, 1998
LRP gene and late-onset Alzheimer's disease
R Woodward, A B Singleton, A M Gibson, et al.
Lancet (London, England)
|
October 7, 1997
Presenilin polymorphisms in Alzheimer's disease
A B Singleton, A M Gibson, A L Atkinson, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
October 26, 2005
First case report of X linked dystonia parkinsonism (XDP) or 'lubag' in Australia
C Plummer, J Bradfield, A B Singleton, et al.
Neurology
|
February 26, 2004
Confirmation of the protective effect of iNOS in an independent cohort of Parkinson disease
S Hague, T Peuralinna, J Eerola, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Canadian Medical Association Journal
|
March 24, 2010
LEAKAGE OF CEREBROSPINAL FLUID THROUGH THE CRIBRIFORM PLATE OF THE ETHMOID BONE
A B Singleton
Neurology
|
August 20, 2008
Yet another spinocerebellar ataxia: the saga continues
O Bandmann, A B Singleton
Clinical Genetics
|
June 10, 2011
Exome sequencing in Parkinson's disease
Jose M Bras, A B Singleton
Neuroscience Letters
|
September 12, 2006
PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease
M M Matarin, A B Singleton, H Houlden
Cell and Tissue Research
|
March 15, 2018
Genetic risk factors in Parkinson's disease
K J Billingsley, S Bandres-Ciga, S Saez-Atienzar, et al.
European Journal of Neurology
|
March 16, 2013
Mutations in EIF4G1 are not a common cause of Parkinson's disease
A Siitonen, E Majounie, M Federoff, et al.
Lancet (London, England)
|
July 31, 1998
LRP gene and late-onset Alzheimer's disease
R Woodward, A B Singleton, A M Gibson, et al.
Lancet (London, England)
|
October 7, 1997
Presenilin polymorphisms in Alzheimer's disease
A B Singleton, A M Gibson, A L Atkinson, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
October 26, 2005
First case report of X linked dystonia parkinsonism (XDP) or 'lubag' in Australia
C Plummer, J Bradfield, A B Singleton, et al.
Neurology
|
February 26, 2004
Confirmation of the protective effect of iNOS in an independent cohort of Parkinson disease
S Hague, T Peuralinna, J Eerola, et al.
Page
of 5