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

Neurogenetics

Showing results (271-280 of 1,080) with videos related to

Pageof 108
Sort By:
Neurogenetics|June 9, 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in miceAndy W Yang, Andrew J Sachs, Arne M Nystuen
Neurogenetics|February 27, 2018
Phenotypic manifestations of the m.8969G>A variantJosef Finsterer, Sinda Zarrouk-Mahjoub
Neurogenetics|December 4, 2017
First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencingStefanie Spiegler, Matthias Rath, Sabine Hoffjan, et al.
Neurogenetics|October 5, 2017
A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutationPaula Sancho, Ana Sánchez-Monteagudo, Antonio Collado, et al.
Neurogenetics|January 8, 2019
Oxygen consumption rate for evaluation of COQ2 variants associated with multiple system atrophyTsutomu Yasuda, Takashi Matsukawa, Jun Mitsui, et al.
Neurogenetics|February 24, 2007
A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patientsAlbena Todorova, Bilyana Georgieva, Ivailo Tournev, et al.
Neurogenetics|February 24, 2007
Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synucleinMelanie Kuhn, Karina Haebig, Michael Bonin, et al.
Neurogenetics|November 4, 2006
Mitochondrial DNA haplogroups and amyotrophic lateral sclerosisPatrick F Chinnery, Catherine Mowbray, Hannah Elliot, et al.
Neurogenetics|September 1, 2006
Familial risks of hospitalization for Parkinson's disease in first-degree relatives: a nationwide follow-up study from SwedenKristina Sundquist, Xinjun Li, Kari Hemminki
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Pageof 108

Showing results (271-280 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|June 9, 2015
Deletion of Inpp5a causes ataxia and cerebellar degeneration in miceAndy W Yang, Andrew J Sachs, Arne M Nystuen
Neurogenetics|February 27, 2018
Phenotypic manifestations of the m.8969G>A variantJosef Finsterer, Sinda Zarrouk-Mahjoub
Neurogenetics|December 4, 2017
First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencingStefanie Spiegler, Matthias Rath, Sabine Hoffjan, et al.
Neurogenetics|October 5, 2017
A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutationPaula Sancho, Ana Sánchez-Monteagudo, Antonio Collado, et al.
Neurogenetics|January 8, 2019
Oxygen consumption rate for evaluation of COQ2 variants associated with multiple system atrophyTsutomu Yasuda, Takashi Matsukawa, Jun Mitsui, et al.
Neurogenetics|February 24, 2007
A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patientsAlbena Todorova, Bilyana Georgieva, Ivailo Tournev, et al.
Neurogenetics|February 24, 2007
Whole genome expression analyses of single- and double-knock-out mice implicate partially overlapping functions of alpha- and gamma-synucleinMelanie Kuhn, Karina Haebig, Michael Bonin, et al.
Neurogenetics|November 4, 2006
Mitochondrial DNA haplogroups and amyotrophic lateral sclerosisPatrick F Chinnery, Catherine Mowbray, Hannah Elliot, et al.
Neurogenetics|September 1, 2006
Familial risks of hospitalization for Parkinson's disease in first-degree relatives: a nationwide follow-up study from SwedenKristina Sundquist, Xinjun Li, Kari Hemminki
Neurogenetics|January 11, 2007
Large germline deletions and duplication in isolated cerebral cavernous malformation patientsU Felbor, S Gaetzner, D J Verlaan, et al.
Pageof 108