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Simone Zittel

Showing results (61-70 of 83) with videos related to

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Parkinsonism & Related Disorders|December 24, 2022
Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variantsTatiana Usnich, Maria Olmedillas, Nathalie Schell, et al.
Neurology|February 6, 2015
Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystoniaNorbert Brüggemann, Andrea Kühn, Susanne A Schneider, et al.
Journal of Neurology|January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literatureFelicitas Becker, Julian Schubert, Pasquale Striano, et al.
Plos One|August 3, 2018
Towards unambiguous reporting of complications related to deep brain stimulation surgery: A retrospective single-center analysis and systematic review of the literatureKatja Engel, Torge Huckhagel, Alessandro Gulberti, et al.
European Journal of Human Genetics : EJHG|August 18, 2011
Identification and functional analysis of novel THAP1 mutationsKatja Lohmann, Nils Uflacker, Alev Erogullari, et al.
Journal of Neurology|February 14, 2016
The role of mutations in COL6A3 in isolated dystoniaKatja Lohmann, Felix Schlicht, Marina Svetel, et al.
Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
<i>RAB32</i> -linked Parkinson's disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteriaTeresa Kleinz, Francesco Cavallieri, Max Borsche, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 17, 2025
RAB32-Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe CriteriaTeresa Kleinz, Francesco Cavallieri, Max Borsche, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Nature Genetics|April 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagyKarla P Figueroa, Caspar Gross, Elena Buena-Atienza, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Parkinsonism & Related Disorders|December 24, 2022
Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variantsTatiana Usnich, Maria Olmedillas, Nathalie Schell, et al.
Neurology|February 6, 2015
Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystoniaNorbert Brüggemann, Andrea Kühn, Susanne A Schneider, et al.
Journal of Neurology|January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literatureFelicitas Becker, Julian Schubert, Pasquale Striano, et al.
Plos One|August 3, 2018
Towards unambiguous reporting of complications related to deep brain stimulation surgery: A retrospective single-center analysis and systematic review of the literatureKatja Engel, Torge Huckhagel, Alessandro Gulberti, et al.
European Journal of Human Genetics : EJHG|August 18, 2011
Identification and functional analysis of novel THAP1 mutationsKatja Lohmann, Nils Uflacker, Alev Erogullari, et al.
Journal of Neurology|February 14, 2016
The role of mutations in COL6A3 in isolated dystoniaKatja Lohmann, Felix Schlicht, Marina Svetel, et al.
Medrxiv : the Preprint Server for Health Sciences|June 26, 2025
<i>RAB32</i> -linked Parkinson's disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteriaTeresa Kleinz, Francesco Cavallieri, Max Borsche, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 17, 2025
RAB32-Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe CriteriaTeresa Kleinz, Francesco Cavallieri, Max Borsche, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Nature Genetics|April 29, 2024
A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagyKarla P Figueroa, Caspar Gross, Elena Buena-Atienza, et al.
Pageof 9