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

Hyun Hor

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Science (New York, N.Y.)|August 15, 2009
Physiology. How much sleep do we need?Hyun Hor, Mehdi Tafti
BMJ Case Reports|December 21, 2018
Absent F-waves in conus medullaris stroke mimicking Guillain-Barré syndromeHyun Hor, Husain Nader, Alexander Andrea Tarnutzer
BMJ Case Reports|December 24, 2024
Varicella zoster infection-associated progressive encephalomyelitis with rigidity and myoclonus in a 6-month follow-upIris Wiederkehr, Hyun Hor, Max Wiederkehr, et al.
Plos One|December 7, 2020
REM sleep behavior in Parkinson disease: Frequent, particularly with higher ageHeide Baumann-Vogel, Hyun Hor, Rositsa Poryazova, et al.
American Journal of Human Genetics|September 13, 2011
A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexyHyun Hor, Luca Bartesaghi, Zoltán Kutalik, et al.
Human Mutation|April 27, 2019
eDiVA-Classification and prioritization of pathogenic variants for clinical diagnosticsMattia Bosio, Oliver Drechsel, Rubayte Rahman, et al.
The Journal of Clinical Investigation|February 18, 2010
Elevated Tribbles homolog 2-specific antibody levels in narcolepsy patientsVesna Cvetkovic-Lopes, Laurence Bayer, Stéphane Dorsaz, et al.
European Journal of Human Genetics : EJHG|January 22, 2015
Rare variants in β-Amyloid precursor protein (APP) and Parkinson's diseaseEva C Schulte, Akio Fukumori, Brit Mollenhauer, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Science (New York, N.Y.)|August 15, 2009
Physiology. How much sleep do we need?Hyun Hor, Mehdi Tafti
BMJ Case Reports|December 21, 2018
Absent F-waves in conus medullaris stroke mimicking Guillain-Barré syndromeHyun Hor, Husain Nader, Alexander Andrea Tarnutzer
BMJ Case Reports|December 24, 2024
Varicella zoster infection-associated progressive encephalomyelitis with rigidity and myoclonus in a 6-month follow-upIris Wiederkehr, Hyun Hor, Max Wiederkehr, et al.
Plos One|December 7, 2020
REM sleep behavior in Parkinson disease: Frequent, particularly with higher ageHeide Baumann-Vogel, Hyun Hor, Rositsa Poryazova, et al.
American Journal of Human Genetics|September 13, 2011
A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexyHyun Hor, Luca Bartesaghi, Zoltán Kutalik, et al.
Human Mutation|April 27, 2019
eDiVA-Classification and prioritization of pathogenic variants for clinical diagnosticsMattia Bosio, Oliver Drechsel, Rubayte Rahman, et al.
The Journal of Clinical Investigation|February 18, 2010
Elevated Tribbles homolog 2-specific antibody levels in narcolepsy patientsVesna Cvetkovic-Lopes, Laurence Bayer, Stéphane Dorsaz, et al.
European Journal of Human Genetics : EJHG|January 22, 2015
Rare variants in β-Amyloid precursor protein (APP) and Parkinson's diseaseEva C Schulte, Akio Fukumori, Brit Mollenhauer, et al.
Human Molecular Genetics|July 19, 2015
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorHyun Hor, Ludmila Francescatto, Luca Bartesaghi, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Pageof 2