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 (911-920 of 1,067) with videos related to

Pageof 107
Sort By:
European Journal of Human Genetics : EJHG|April 19, 2019
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2Alessia Peretti, Maud Perie, Didier Vincent, et al.
Annals of Clinical and Translational Neurology|March 19, 2026
Cracking the Code: Genotype-Phenotype Correlation Models in SarcoglycanopathiesLeonela Luce, Goknur Selen Kocak, José Verdú-Díaz, et al.
Frontiers in Pharmacology|June 13, 2022
Correlation of Dyslipidemia and Inflammation With Obstructive Sleep Apnea SeverityViseslav Popadic, Milica Brajkovic, Slobodan Klasnja, et al.
Biochemical Pharmacology|May 31, 2021
Pharmacological inhibition of fatty acid oxidation reduces atherosclerosis progression by suppression of macrophage NLRP3 inflammasome activationPhilipp J Hohensinner, Max Lenz, Patrick Haider, et al.
Nature Immunology|May 16, 2018
Cross-specificity of protective human antibodies against Klebsiella pneumoniae LPS O-antigenTim Rollenske, Valeria Szijarto, Jolanta Lukasiewicz, et al.
Iscience|July 14, 2025
Inhibition of dimeric SARS-CoV-2 Mpro displays positive cooperativity and a mixture of covalent and non-covalent bindingKrishna M Padmanabha Das, Jun Chen, Paul S Charifson, et al.
Journal of Neuromuscular Diseases|July 8, 2025
REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in FranceLamiae Grimaldi, Rocio Garcia-Uzquiano, Marta Gomez-Garcia de la Banda, et al.
Journal of Neurology|March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagyGorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
International Journal of Molecular Sciences|December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only ExonsAurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Neuromuscular Disorders : NMD|November 13, 2025
Novel missense variants associated with GNE myopathyJohanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Pageof 107

Showing results (911-920 of 1,067) with videos related to

Sort By:
Pageof 107
European Journal of Human Genetics : EJHG|April 19, 2019
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2Alessia Peretti, Maud Perie, Didier Vincent, et al.
Annals of Clinical and Translational Neurology|March 19, 2026
Cracking the Code: Genotype-Phenotype Correlation Models in SarcoglycanopathiesLeonela Luce, Goknur Selen Kocak, José Verdú-Díaz, et al.
Frontiers in Pharmacology|June 13, 2022
Correlation of Dyslipidemia and Inflammation With Obstructive Sleep Apnea SeverityViseslav Popadic, Milica Brajkovic, Slobodan Klasnja, et al.
Biochemical Pharmacology|May 31, 2021
Pharmacological inhibition of fatty acid oxidation reduces atherosclerosis progression by suppression of macrophage NLRP3 inflammasome activationPhilipp J Hohensinner, Max Lenz, Patrick Haider, et al.
Nature Immunology|May 16, 2018
Cross-specificity of protective human antibodies against Klebsiella pneumoniae LPS O-antigenTim Rollenske, Valeria Szijarto, Jolanta Lukasiewicz, et al.
Iscience|July 14, 2025
Inhibition of dimeric SARS-CoV-2 Mpro displays positive cooperativity and a mixture of covalent and non-covalent bindingKrishna M Padmanabha Das, Jun Chen, Paul S Charifson, et al.
Journal of Neuromuscular Diseases|July 8, 2025
REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in FranceLamiae Grimaldi, Rocio Garcia-Uzquiano, Marta Gomez-Garcia de la Banda, et al.
Journal of Neurology|March 22, 2024
Phenotype variability and natural history of X-linked myopathy with excessive autophagyGorka Fernández-Eulate, Girolamo Alfieri, Marco Spinazzi, et al.
International Journal of Molecular Sciences|December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only ExonsAurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Neuromuscular Disorders : NMD|November 13, 2025
Novel missense variants associated with GNE myopathyJohanna Ranta-Aho, Viviana Cetrangolo, Luca Bello, et al.
Pageof 107