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Katrin Beyer

Showing results (51-60 of 56) with videos related to

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Brain Pathology (Zurich, Switzerland)|December 16, 2025
14-3-3σ up-regulation in the temporal cortex associates with tau pathology and reactive astroglia in Lewy body disordersLaura Marsal-García, Jorge Mena, Carol-Ann Lao, et al.
Parkinsonism & Related Disorders|September 7, 2023
Peripheral α-synuclein isoforms are potential biomarkers for diagnosis and prognosis of isolated REM sleep behavior disorderLaura Arnaldo, Aintzane Urbizu, Mònica Serradell, et al.
Journal of Neurology|June 18, 2009
Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain)Eduardo López-Laso, Juan José Ochoa-Sepúlveda, Juan José Ochoa-Amor, et al.
Journal of Neurology|May 11, 2011
Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa diseaseEduardo López-Laso, Araceli Sánchez-Raya, Juan Antonio Moriana, et al.
NPJ Genomic Medicine|April 9, 2026
Unraveling the genetic architecture of non-Huntington chorea: a biobank-scale study of rare variants and repeat expansionsFulya Akçimen, Monica Diez-Fairen, Ignacio Alvarez, et al.
Movement Disorders Clinical Practice|June 19, 2023
Cognitive and Motor Decline in Dementia with Lewy Bodies and Parkinson's Disease DementiaMaria Camila Gonzalez, Diego Alejandro Tovar-Rios, Guido Alves, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Brain Pathology (Zurich, Switzerland)|December 16, 2025
14-3-3σ up-regulation in the temporal cortex associates with tau pathology and reactive astroglia in Lewy body disordersLaura Marsal-García, Jorge Mena, Carol-Ann Lao, et al.
Parkinsonism & Related Disorders|September 7, 2023
Peripheral α-synuclein isoforms are potential biomarkers for diagnosis and prognosis of isolated REM sleep behavior disorderLaura Arnaldo, Aintzane Urbizu, Mònica Serradell, et al.
Journal of Neurology|June 18, 2009
Segawa syndrome due to mutation Q89X in the GCH1 gene: a possible founder effect in Córdoba (southern Spain)Eduardo López-Laso, Juan José Ochoa-Sepúlveda, Juan José Ochoa-Amor, et al.
Journal of Neurology|May 11, 2011
Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa diseaseEduardo López-Laso, Araceli Sánchez-Raya, Juan Antonio Moriana, et al.
NPJ Genomic Medicine|April 9, 2026
Unraveling the genetic architecture of non-Huntington chorea: a biobank-scale study of rare variants and repeat expansionsFulya Akçimen, Monica Diez-Fairen, Ignacio Alvarez, et al.
Movement Disorders Clinical Practice|June 19, 2023
Cognitive and Motor Decline in Dementia with Lewy Bodies and Parkinson's Disease DementiaMaria Camila Gonzalez, Diego Alejandro Tovar-Rios, Guido Alves, et al.
Pageof 6