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

Stojkovic

Showing results (921-930 of 1,067) with videos related to

Pageof 107
Sort By:
Haematologica|January 25, 2020
Alternative activation of human macrophages enhances tissue factor expression and production of extracellular vesiclesPhilipp J Hohensinner, Julia Mayer, Julia Kichbacher, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
European Heart Journal|December 13, 2016
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1Karim Wahbi, Dominique Babuty, Vincent Probst, et al.
Journal of the American Heart Association|August 15, 2023
Prognosis of Right Ventricular Systolic Dysfunction in Patients With Duchenne Muscular DystrophyAbdallah Fayssoil, Nicolas Mansencal, Lee S Nguyen, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Diagnostics (Basel, Switzerland)|May 27, 2026
Lumen-Stent Mismatch Affects Long-Term Strut Healing After Primary PCI of Left Main Lesions: An Exploratory Follow-Up OCT StudyZlatko Mehmedbegovic, Vladan Vukcevic, Sinisa Stojkovic, et al.
Molecular Reproduction and Development|March 27, 2003
Nucleolar proteins and ultrastructure in bovine in vivo developed, in vitro produced, and parthenogenetic cleavage-stage embryosJ Laurincik, F Schmoll, E Mahabir, et al.
Pageof 107

Showing results (921-930 of 1,067) with videos related to

Sort By:
Pageof 107
Haematologica|January 25, 2020
Alternative activation of human macrophages enhances tissue factor expression and production of extracellular vesiclesPhilipp J Hohensinner, Julia Mayer, Julia Kichbacher, et al.
Revue Neurologique|September 10, 2013
[Charcot-Marie-Tooth disease associated with periaxin mutations (CMT4F): Clinical, electrophysiological and genetic analysis of 24 patients]M Renouil, T Stojkovic, M L Jacquemont, et al.
European Heart Journal|December 13, 2016
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1Karim Wahbi, Dominique Babuty, Vincent Probst, et al.
Journal of the American Heart Association|August 15, 2023
Prognosis of Right Ventricular Systolic Dysfunction in Patients With Duchenne Muscular DystrophyAbdallah Fayssoil, Nicolas Mansencal, Lee S Nguyen, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Journal of Neurology|September 1, 2019
Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigationsN C Voermans, R C van der Bilt, J IJspeert, et al.
American Journal of Human Genetics|September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophyLucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Diagnostics (Basel, Switzerland)|May 27, 2026
Lumen-Stent Mismatch Affects Long-Term Strut Healing After Primary PCI of Left Main Lesions: An Exploratory Follow-Up OCT StudyZlatko Mehmedbegovic, Vladan Vukcevic, Sinisa Stojkovic, et al.
Molecular Reproduction and Development|March 27, 2003
Nucleolar proteins and ultrastructure in bovine in vivo developed, in vitro produced, and parthenogenetic cleavage-stage embryosJ Laurincik, F Schmoll, E Mahabir, et al.
Pageof 107