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Carolin Gabbert

Showing results (11-20 of 19) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser ParkinsonismTheresa Lüth, Carolin Gabbert, Sebastian Koch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 26, 2022
Ca2+ imaging of self and other in medial prefrontal cortex during social dominance interactions in a tube testNuria Garcia-Font, Rufus Mitchell-Heggs, Kapil Saxena, et al.
Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Medrxiv : the Preprint Server for Health Sciences|October 1, 2025
Validation of a Mitochondrial Polygenic Score for Parkinson's DiseaseJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2025
Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across AncestriesJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, 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.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's diseaseShreya Menon, Adam W Turner, Serena H Chang, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser ParkinsonismTheresa Lüth, Carolin Gabbert, Sebastian Koch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 26, 2022
Ca2+ imaging of self and other in medial prefrontal cortex during social dominance interactions in a tube testNuria Garcia-Font, Rufus Mitchell-Heggs, Kapil Saxena, et al.
Annals of Clinical and Translational Neurology|February 7, 2026
Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural VariantsAndré Fienemann, Theresa Lüth, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Medrxiv : the Preprint Server for Health Sciences|October 1, 2025
Validation of a Mitochondrial Polygenic Score for Parkinson's DiseaseJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2025
Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across AncestriesJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, 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.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's diseaseShreya Menon, Adam W Turner, Serena H Chang, et al.
Pageof 2