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Niccolo E Mencacci

Showing results (21-30 of 29) with videos related to

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NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.
Plos One|August 13, 2013
Dopaminergic neuronal imaging in genetic Parkinson's disease: insights into pathogenesisAlisdair McNeill, Ruey-Meei Wu, Kai-Yuan Tzen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Nature Genetics|May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.
Nature Genetics|December 20, 2016
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Dystonia Linked to EIF4A2 Haploinsufficiency: A Disorder of Protein Translation DysfunctionPhilip Harrer, Matej Škorvánek, Volker Kittke, et al.
Plos One|August 13, 2013
Dopaminergic neuronal imaging in genetic Parkinson's disease: insights into pathogenesisAlisdair McNeill, Ruey-Meei Wu, Kai-Yuan Tzen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
Nature Genetics|May 27, 2017
Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.
Nature Genetics|December 20, 2016
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaEsther Meyer, Keren J Carss, Julia Rankin, et al.
Pageof 3