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Plos One|April 1, 2017
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegiaZafar Iqbal, Siri L Rydning, Iselin M Wedding, et al.Neurologia I Neurochirurgia Polska|February 4, 2021
Genetics of Parkinson's disease in the Polish populationŁukasz M Milanowski, Owen A Ross, Andrzej Friedman, et al.Frontiers in Stroke|January 16, 2026
Plasma apolipoprotein E and monocyte chemoattractant protein-1 levels in young people with HIV and ischemic stroke in Lusaka, ZambiaStanley Zimba, Owen Ngalamika, Emmanuel Mukambo, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2017
Regional analysis and genetic association of nigrostriatal degeneration in Lewy body diseaseKoji Kasanuki, Michael G Heckman, Nancy N Diehl, et al.Movement Disorders Clinical Practice|July 17, 2018
Multiple Microelectrode Recordings in STN-DBS Surgery for Parkinson's Disease: A Randomized StudySilje Bjerknes, Mathias Toft, Ane E Konglund, et al.Med (New York, N.Y.)|October 14, 2025
The role of mitochondrial genetics in Parkinson's disease: Long-read sequencing as an emerging methodNgan Le Kim Tran, Marka van Blitterswijk, Wolfdieter Springer, et al.Parkinsonism & Related Disorders|October 26, 2010
Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's diseaseKenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, et al.Parkinsonism & Related Disorders|September 18, 2017
Parkinson's disease susceptibility variants and severity of Lewy body pathologyMichael G Heckman, Koji Kasanuki, Nancy N Diehl, et al.Neurologia I Neurochirurgia Polska|April 23, 2018
Anticipation in a family with primary familial brain calcification caused by an SLC20A2 variantTakuya Konno, Patrick R Blackburn, Todd D Rozen, et al.Neuroscience Letters|January 6, 2007
Phenotypic associations of tau and ApoE in Parkinson's diseaseSpiridon Papapetropoulos, Matthew J Farrer, Jeremy T Stone, et al.Pageof 49