Researchers
Ivanović, Vukan
Results 1-20 of 30
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Hidden diagnoses among patients with double seronegative myasthenia gravis![]() | Ivanović, Vukan | Article | 22M22 |
| 2026 | Plasma miR-150-5p as a biomarker for immunosuppressive therapy response in acetylcholine receptor positive myasthenia gravis: a long-term prospective longitudinal study![]() | Garai, Nemanja | Article | 21a+M21a+ |
| 2026 | Response to Letter to the Editor: Letter by Ru and Zhang regarding article, "Plasma miR-150-5p as a biomarker for immunosuppressive therapy response in acetylcholine receptor positive myasthenia gravis: a long-term prospective longitudinal study"![]() | Garai, Nemanja | Contribution to periodical | 21a+M21a+ |
| 2025 | Hereditary neuropathies in Serbian population![]() | Vukojević, Milica | Conference Paper | Mp. category will be shown later |
| 2025 | Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the Phenotype![]() | Record, Christopher J.; ...; Perić, Stojan | Article | 21a+M21a+ |
| 2025 | Longitudinal Chronic Acquired Polyneuropathy Patient Reported Index (CAPPRI) Evaluation in Active Chronic Inflammatory Demyelinating Polyneuropathy![]() | Božović, Ivo | Conference Paper | Mp. category will be shown later |
| 2025 | Evaluating award-winning doctoral theses to reveal PhD research landscape: A case study of the Faculty of Medicine, University of Belgrade![]() | Milovanović, Petar | Article | 23M23 |
| 2025 | Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models![]() | Tedesco, Barbara; Perić, Stojan | Article | 21M21 |
| 2025 | Screening for Pompe disease in Serbian patients with limb-girdle muscle weakness![]() | Sekulić, Aleksandar; Virić, Vanja | Article | 22M22 |
| 2024 | Screening for Pompe disease and its differential diagnoses![]() | Sekulić, A.; Todorović, T.; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Article | 22M22 |
| 2024 | Bulbar-onset amyotrophic lateral sclerosis in a patient with genetically confirmed Huntington's disease: a case study![]() | Božović, Ivo | Article | Mp. category will be shown later |
| 2024 | Impact of discontinuation and reintroduction of alglucoidase alpha in patients with late-onset Pompe disease![]() | Andrejić, Nikola; Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2024 | C9orf72 genetic screening in patients with ALS/FTD phenotype from Serbia![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2023 | EPR-210 Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2023 | Update on Therapy for Myotonic Dystrophy Type 1![]() | Ivanović, Vukan | Article | 22M22 |
| 2023 | Autophagy Regulation in Peripheral Blood Mononuclear Cells of Patients with Chronic Inflammatory Demyelinating Polyneuropathy![]() | Milošević, Emina | Conference Paper | Mp. category will be shown later |
| 2023 | Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in Serbia![]() | Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2023 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2022 | Cognitive assessment in patients with myotonic dystrophy type 2![]() | Perić, Stojan | Article | 21M21 |
