Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Thomas Gasser

Showing results (231-240 of 476) with videos related to

Pageof 48
Sort By:
The Lancet. Neurology|April 9, 2008
The specificity and sensitivity of transcranial ultrasound in the differential diagnosis of Parkinson's disease: a prospective blinded studyAlexandra Gaenslen, Barbara Unmuth, Jana Godau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
European Journal of Neurology|July 1, 2024
Association of elevated cerebrospinal fluid levels of the longevity protein α-Klotho with a delayed onset of cognitive impairment in Parkinson's disease patientsMilan Zimmermann, Madeleine Fandrich, Meike Jakobi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Involuntary eyelid closure after STN-DBS: evidence for different pathophysiological entitiesDaniel Weiss, Tobias Wächter, Sorin Breit, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Journal of Neurology|February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutationJügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Neuroscience Letters|May 3, 2003
Lack of association of interleukin-10 promoter region polymorphisms with Alzheimer's diseaseCandan Depboylu, Yansheng Du, Ulrich Müller, et al.
Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.
Brain : a Journal of Neurology|October 28, 2005
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*Daniela Berg, Katherine J Schweitzer, Petra Leitner, et al.
Neurology|November 10, 2017
SNPs in Aβ clearance proteins: Lower CSF Aβ<sub>1-42</sub> levels and earlier onset of dementia in PDKathrin Brockmann, Stefanie Lerche, Sarah Selina Dilger, et al.
Pageof 48

Showing results (231-240 of 476) with videos related to

Sort By:
Pageof 48
The Lancet. Neurology|April 9, 2008
The specificity and sensitivity of transcranial ultrasound in the differential diagnosis of Parkinson's disease: a prospective blinded studyAlexandra Gaenslen, Barbara Unmuth, Jana Godau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2018
HPCA confirmed as a genetic cause of DYT2-like dystonia phenotypeBurcu Atasu, Hasmet Hanagasi, Basar Bilgic, et al.
European Journal of Neurology|July 1, 2024
Association of elevated cerebrospinal fluid levels of the longevity protein α-Klotho with a delayed onset of cognitive impairment in Parkinson's disease patientsMilan Zimmermann, Madeleine Fandrich, Meike Jakobi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Involuntary eyelid closure after STN-DBS: evidence for different pathophysiological entitiesDaniel Weiss, Tobias Wächter, Sorin Breit, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Journal of Neurology|February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutationJügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Neuroscience Letters|May 3, 2003
Lack of association of interleukin-10 promoter region polymorphisms with Alzheimer's diseaseCandan Depboylu, Yansheng Du, Ulrich Müller, et al.
Parkinsonism & Related Disorders|December 18, 2017
Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in TurkeyChristoph Kessler, Burcu Atasu, Hasmet Hanagasi, et al.
Brain : a Journal of Neurology|October 28, 2005
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*Daniela Berg, Katherine J Schweitzer, Petra Leitner, et al.
Neurology|November 10, 2017
SNPs in Aβ clearance proteins: Lower CSF Aβ<sub>1-42</sub> levels and earlier onset of dementia in PDKathrin Brockmann, Stefanie Lerche, Sarah Selina Dilger, et al.
Pageof 48