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O A Ross

Showing results (11-20 of 36) with videos related to

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Experimental Gerontology|June 19, 2001
Mitochondrial DNA polymorphism: its role in longevity of the Irish populationO A Ross, R McCormack, M D Curran, et al.
Neuropathology and Applied Neurobiology|January 18, 2006
Lrrk2 R1441 substitution and progressive supranuclear palsyO A Ross, A J Whittle, S A Cobb, et al.
Neurology|January 16, 2008
Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementiaT Obi, K Nishioka, O A Ross, et al.
European Journal of Neurology|August 14, 2012
Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic strokeM G Heckman, A I Soto-Ortolaza, N N Diehl, et al.
Neurology|September 2, 2011
Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALSM DeJesus-Hernandez, P Desaro, A Johnston, et al.
European Journal of Neurology|March 7, 2018
Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalitiesT Konno, T Miura, A M Harriott, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 26, 2006
Pathogenic Lrrk2 substitutions and Amyotrophic lateral sclerosisA J Whittle, O A Ross, A Naini, et al.
Neurology|October 25, 2006
Parkinsonism, Lrrk2 G2019S, and tau neuropathologyA Rajput, D W Dickson, C A Robinson, et al.
European Journal of Neurology|April 29, 2006
LRRK2 mutations are a common cause of Parkinson's disease in SpainI F Mata, O A Ross, J Kachergus, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 31, 2008
Clinical characteristics of Parkinson's disease among Jewish Ethnic groups in IsraelR Djaldetti, S Hassin-Baer, M J Farrer, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Experimental Gerontology|June 19, 2001
Mitochondrial DNA polymorphism: its role in longevity of the Irish populationO A Ross, R McCormack, M D Curran, et al.
Neuropathology and Applied Neurobiology|January 18, 2006
Lrrk2 R1441 substitution and progressive supranuclear palsyO A Ross, A J Whittle, S A Cobb, et al.
Neurology|January 16, 2008
Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementiaT Obi, K Nishioka, O A Ross, et al.
European Journal of Neurology|August 14, 2012
Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic strokeM G Heckman, A I Soto-Ortolaza, N N Diehl, et al.
Neurology|September 2, 2011
Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALSM DeJesus-Hernandez, P Desaro, A Johnston, et al.
European Journal of Neurology|March 7, 2018
Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalitiesT Konno, T Miura, A M Harriott, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 26, 2006
Pathogenic Lrrk2 substitutions and Amyotrophic lateral sclerosisA J Whittle, O A Ross, A Naini, et al.
Neurology|October 25, 2006
Parkinsonism, Lrrk2 G2019S, and tau neuropathologyA Rajput, D W Dickson, C A Robinson, et al.
European Journal of Neurology|April 29, 2006
LRRK2 mutations are a common cause of Parkinson's disease in SpainI F Mata, O A Ross, J Kachergus, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 31, 2008
Clinical characteristics of Parkinson's disease among Jewish Ethnic groups in IsraelR Djaldetti, S Hassin-Baer, M J Farrer, et al.
Pageof 4