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Jovan Pesovic

Showing results (21-30 of 26) with videos related to

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Journal of Neuromuscular Diseases|September 25, 2018
Myotonic Dystrophy Type 2 - Data from the Serbian RegistryIvo Bozovic, Stojan Peric, Jovan Pesovic, et al.
Neuromuscular Disorders : NMD|July 25, 2022
Cognitive assessment in patients with myotonic dystrophy type 2Stojan Peric, Ilija Gunjic, Neda Delic, et al.
Molecular Neurobiology|April 25, 2025
Causal Variants in CHRNA1 and CHRNB1 Genes for Anti-acetylcholine Receptor Antibody Positive Myasthenia Gravis: Evidence from Bayesian Fine-Mapping and Genetic Association StudyNemanja Garai, Kristina Petrovic, Stojan Peric, et al.
Genes|August 26, 2022
<i>LTBP4</i>, <i>SPP1</i>, and <i>CD40</i> Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian PatientsAna Kosac, Jovan Pesovic, Lana Radenkovic, et al.
Iscience|December 30, 2024
Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneityJudit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Iscience|June 4, 2024
Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneityJudit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of Neuromuscular Diseases|September 25, 2018
Myotonic Dystrophy Type 2 - Data from the Serbian RegistryIvo Bozovic, Stojan Peric, Jovan Pesovic, et al.
Neuromuscular Disorders : NMD|July 25, 2022
Cognitive assessment in patients with myotonic dystrophy type 2Stojan Peric, Ilija Gunjic, Neda Delic, et al.
Molecular Neurobiology|April 25, 2025
Causal Variants in CHRNA1 and CHRNB1 Genes for Anti-acetylcholine Receptor Antibody Positive Myasthenia Gravis: Evidence from Bayesian Fine-Mapping and Genetic Association StudyNemanja Garai, Kristina Petrovic, Stojan Peric, et al.
Genes|August 26, 2022
<i>LTBP4</i>, <i>SPP1</i>, and <i>CD40</i> Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian PatientsAna Kosac, Jovan Pesovic, Lana Radenkovic, et al.
Iscience|December 30, 2024
Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneityJudit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Iscience|June 4, 2024
Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneityJudit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, et al.
Pageof 3