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Neurobiology of Aging
|
October 21, 2018
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease
Victoria Berge-Seidl, Lasse Pihlstrøm, Zbigniew K Wszolek, et al.
Lancet (London, England)
|
April 7, 2005
LRRK2 mutations and Parkinsonism
Mathias Toft, Ignacio F Mata, Jennifer M Kachergus, et al.
Annals of Clinical and Translational Neurology
|
February 5, 2025
Epigenome-wide association study, meta-analysis, and multiscore profiling of whole blood in Parkinson's disease
Ingeborg Haugesag Lie, Manuela M X Tan, Maren Stolp Andersen, et al.
Journal of Neuroscience Research
|
March 28, 2007
MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease
Linda R White, Mathias Toft, Sylvia N Kvam, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
June 11, 2026
The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological Findings
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, et al.
Journal of Parkinson'S Disease
|
August 14, 2013
Found in transcription: accurate Parkinson's disease classification in peripheral blood
Magdalena Kauczynska Karlsson, Praveen Sharma, Jan Aasly, et al.
European Stroke Journal
|
January 30, 2026
Presenting symptoms and diagnostic accuracy of prehospital stroke scales for patients with suspected mild minor stroke
Helge Fagerheim Bugge, Mona Guterud, Karianne Larsen, et al.
European Stroke Journal
|
August 11, 2025
Presenting symptoms and diagnostic accuracy of prehospital stroke scales for patients with suspected mild minor stroke
Helge Fagerheim Bugge, Mona Guterud, Karianne Larsen, et al.
European Journal of Human Genetics : EJHG
|
June 23, 2016
Rare variants in dementia genes and Parkinson's disease
Zafar Iqbal, Lasse Pihlstrøm, Aina Rengmark, et al.
Neuroscience Letters
|
February 28, 2007
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway
Kristoffer Haugarvoll, Mathias Toft, Owen A Ross, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 129) with videos related to
Sort By:
Page
of 13
Neurobiology of Aging
|
October 21, 2018
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease
Victoria Berge-Seidl, Lasse Pihlstrøm, Zbigniew K Wszolek, et al.
Lancet (London, England)
|
April 7, 2005
LRRK2 mutations and Parkinsonism
Mathias Toft, Ignacio F Mata, Jennifer M Kachergus, et al.
Annals of Clinical and Translational Neurology
|
February 5, 2025
Epigenome-wide association study, meta-analysis, and multiscore profiling of whole blood in Parkinson's disease
Ingeborg Haugesag Lie, Manuela M X Tan, Maren Stolp Andersen, et al.
Journal of Neuroscience Research
|
March 28, 2007
MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease
Linda R White, Mathias Toft, Sylvia N Kvam, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
June 11, 2026
The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway - A Description of Demographic, Medical, and Neurological Findings
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, et al.
Journal of Parkinson'S Disease
|
August 14, 2013
Found in transcription: accurate Parkinson's disease classification in peripheral blood
Magdalena Kauczynska Karlsson, Praveen Sharma, Jan Aasly, et al.
European Stroke Journal
|
January 30, 2026
Presenting symptoms and diagnostic accuracy of prehospital stroke scales for patients with suspected mild minor stroke
Helge Fagerheim Bugge, Mona Guterud, Karianne Larsen, et al.
European Stroke Journal
|
August 11, 2025
Presenting symptoms and diagnostic accuracy of prehospital stroke scales for patients with suspected mild minor stroke
Helge Fagerheim Bugge, Mona Guterud, Karianne Larsen, et al.
European Journal of Human Genetics : EJHG
|
June 23, 2016
Rare variants in dementia genes and Parkinson's disease
Zafar Iqbal, Lasse Pihlstrøm, Aina Rengmark, et al.
Neuroscience Letters
|
February 28, 2007
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway
Kristoffer Haugarvoll, Mathias Toft, Owen A Ross, et al.
Page
of 13