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Katja Lohmann

Showing results (211-220 of 267) with videos related to

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Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Parkinsonism & Related Disorders|May 23, 2020
Private variants in PRKN are associated with late-onset Parkinson's diseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
The Lancet. Neurology|October 24, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinicShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, 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.
Movement Disorders Clinical Practice|May 23, 2024
Sex Differences in DystoniaGamze Kilic-Berkmen, Laura M Scorr, Lucas McKay, 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.
NPJ Parkinson'S Disease|August 1, 2025
Large-scale copy number variant analysis in genes linked to Parkinson´s diseaseZied Landoulsi, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Annals of Neurology|April 12, 2019
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonismAna Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
Brain : a Journal of Neurology|December 8, 2022
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's diseaseJoanne Trinh, Andrew A Hicks, Inke R König, et al.
Pageof 27

Showing results (211-220 of 267) with videos related to

Sort By:
Pageof 27
Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Parkinsonism & Related Disorders|May 23, 2020
Private variants in PRKN are associated with late-onset Parkinson's diseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
The Lancet. Neurology|October 24, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinicShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, 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.
Movement Disorders Clinical Practice|May 23, 2024
Sex Differences in DystoniaGamze Kilic-Berkmen, Laura M Scorr, Lucas McKay, 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.
NPJ Parkinson'S Disease|August 1, 2025
Large-scale copy number variant analysis in genes linked to Parkinson´s diseaseZied Landoulsi, Katja Lohmann, Eva-Juliane Vollstedt, et al.
Annals of Neurology|April 12, 2019
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonismAna Westenberger, Charles Jourdan Reyes, Gerard Saranza, et al.
Brain : a Journal of Neurology|December 8, 2022
Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson's diseaseJoanne Trinh, Andrew A Hicks, Inke R König, et al.
Pageof 27