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

Erik Freier

Showing results (21-30 of 24) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 24 results.
Cells|December 24, 2021
Phenotypical and Myopathological Consequences of Compound Heterozygous Missense and Nonsense Variants in <i>SLC18A3</i>Adela Della Marina, Annabelle Arlt, Ulrike Schara-Schmidt, et al.
International Journal of Molecular Sciences|May 28, 2022
CARS Imaging Advances Early Diagnosis of Cardiac Manifestation of Fabry DiseaseElen Tolstik, Nairveen Ali, Shuxia Guo, et al.
Skeletal Muscle|August 30, 2018
Biochemical and pathological changes result from mutated Caveolin-3 in muscleJosé Andrés González Coraspe, Joachim Weis, Mary E Anderson, et al.
Neuropathology and Applied Neurobiology|January 11, 2021
Molecular pathophysiology of human MICU1 deficiencyNicolai Kohlschmidt, Miriam Elbracht, Artur Czech, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Cells|December 24, 2021
Phenotypical and Myopathological Consequences of Compound Heterozygous Missense and Nonsense Variants in <i>SLC18A3</i>Adela Della Marina, Annabelle Arlt, Ulrike Schara-Schmidt, et al.
International Journal of Molecular Sciences|May 28, 2022
CARS Imaging Advances Early Diagnosis of Cardiac Manifestation of Fabry DiseaseElen Tolstik, Nairveen Ali, Shuxia Guo, et al.
Skeletal Muscle|August 30, 2018
Biochemical and pathological changes result from mutated Caveolin-3 in muscleJosé Andrés González Coraspe, Joachim Weis, Mary E Anderson, et al.
Neuropathology and Applied Neurobiology|January 11, 2021
Molecular pathophysiology of human MICU1 deficiencyNicolai Kohlschmidt, Miriam Elbracht, Artur Czech, et al.
Pageof 3