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Ignacio F Mata

Showing results (101-110 of 128) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
MEX-PD: A National Network for the Epidemiological & Genetic Research of Parkinson's DiseaseAlejandra Lázaro-Figueroa, Paula Reyes-Pérez, Eugenia Morelos-Figaredo, et al.
Molecular Neurodegeneration|September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's diseaseIgnacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's diseaseIgnacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Parkinsonism & Related Disorders|June 3, 2011
Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin AmericaIgnacio F Mata, Greggory J Wilhoite, Dora Yearout, et al.
Neurology|February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseasesAlberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk ScoresPaula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
Neurology|October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathologyDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
NPJ Parkinson'S Disease|July 3, 2025
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scoresPaula Saffie-Awad, Spencer M Grant, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2024
Parkinson's Disease Gene Screening in Familial Cases from Central and South AmericaOswaldo Lorenzo-Betancor, Seysha Mehta, Janvi Ramchandra, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Pageof 13

Showing results (101-110 of 128) with videos related to

Sort By:
Pageof 13
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
MEX-PD: A National Network for the Epidemiological & Genetic Research of Parkinson's DiseaseAlejandra Lázaro-Figueroa, Paula Reyes-Pérez, Eugenia Morelos-Figaredo, et al.
Molecular Neurodegeneration|September 25, 2015
The RAB39B p.G192R mutation causes X-linked dominant Parkinson's diseaseIgnacio F Mata, Yongwoo Jang, Chun-Hyung Kim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2012
Common variation in the LRRK2 gene is a risk factor for Parkinson's diseaseIgnacio F Mata, Harvey Checkoway, Carolyn M Hutter, et al.
Parkinsonism & Related Disorders|June 3, 2011
Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin AmericaIgnacio F Mata, Greggory J Wilhoite, Dora Yearout, et al.
Neurology|February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseasesAlberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk ScoresPaula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
Neurology|October 5, 2012
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathologyDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
NPJ Parkinson'S Disease|July 3, 2025
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scoresPaula Saffie-Awad, Spencer M Grant, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2024
Parkinson's Disease Gene Screening in Familial Cases from Central and South AmericaOswaldo Lorenzo-Betancor, Seysha Mehta, Janvi Ramchandra, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Pageof 13