Researchers
Milić-Rašić, Vedrana
Results 1-20 of 84
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia![]() | Kovačević, Gordana | Article | 21M21 |
| 2024 | Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia![]() | Brkušanin, Miloš | Article | 21M21 |
| 2024 | Osnovi neurološkog pregleda![]() | Kostić, Vladimir | Text book | Mp. category will be shown later |
| 2022 | LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients![]() | Kosac, Ana | Article | 22M22 |
| 2021 | Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3![]() | Đorđević, Stefan A.; Milić-Rasić, Vedrana M. | Article | 22M22 |
| 2021 | Osnovi neurološkog pregleda![]() | Kostić, Vladimir | Text book | Mp. category will be shown later |
| 2021 | Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response![]() | Beijer, Danique; Agnew, Thomas; Rack, Johannes Gregor Matthias; Prokhorova, Evgeniia; Deconinck, Tine; Ceulemans, Berten; Perić, Stojan Z.
Baets, Jonathan;
| Article | 21aM21a |
| 2021 | Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3![]() | Đorđević, Stefan A.; Milić-Rašić, Vedrana M. | Article | 21M21 |
| 2020 | Neurologija : za studente medicine![]() | Kostić, Vladimir
Kozić, Duško
| Text book | Mp. category will be shown later |
| 2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies![]() | Maksić, Jasmina | Article | 23M23 |
| 2019 | Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia![]() | Perić, Stojan | Article | Mp. category will be shown later |
| 2018 | Structure of the 5q13.2 segmental duplication as a modifier of the phenotype of spinal muscular atrophy and amyotrophic lateral sclerosis | Brkušanin, Miloš Đ. | Conference Paper | Mp. category will be shown later |
| 2018 | Duchenne muscular dystrophy and the heart - how to visualize better? - Case series report | Kosać, Ana | Conference Paper | Mp. category will be shown later |
| 2018 | Features of the Serbian cohort of patients with calpainopathy![]() | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2018 | A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population | Pešović, Jovan Z. | Conference Paper | Mp. category will be shown later |
| 2018 | Neurologija: za studente medicine![]() | Kostić, Vladimir
Kozić, Duško
| Text book | Mp. category will be shown later |
| 2018 | Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report | Kresojević, Nikola; Petrović, Igor; Dobričić, Valerija; Tomić, Aleksandra; Branković, Vesna; Milić Rašić, Vedrana | Article | Mp. category will be shown later |
| 2017 | Genotype-phenotype correlation in Friedreich's ataxia![]() | Kovačević, G.; Todorović, S.; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2017 | Synergistic influence of the SMN2 and SERF1A gene copy number on childhood-onset spinal muscular atrophy | Brkušanin, Miloš Đ. | Conference Paper | Mp. category will be shown later |
| 2017 | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia![]() | Dobričić, Valerija | Article | 21aM21a |
