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

Jens Teichler

Showing results (1-10 of 3) with videos related to

Pageof 1
Sort By:
BMJ Case Reports|July 4, 2012
X-linked adrenoleukodystrophy presenting as Addison's diseaseBernhard Kaspar Morell, Jens Teichler, Kemal Budak, et al.
Neuropediatrics|October 20, 2015
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing PanencephalitisMartin Häusler, Ayse Aksoy, Michael Alber, et al.
Human Mutation|May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizuresJulian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
BMJ Case Reports|July 4, 2012
X-linked adrenoleukodystrophy presenting as Addison's diseaseBernhard Kaspar Morell, Jens Teichler, Kemal Budak, et al.
Neuropediatrics|October 20, 2015
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing PanencephalitisMartin Häusler, Ayse Aksoy, Michael Alber, et al.
Human Mutation|May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizuresJulian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Pageof 1