Researchers
Stojanović, Vidosava
Results 21-40 of 194
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | Clinical score for early diagnosis of myotonic dystrophy type 2![]() | Ivanović, Vukan | Article | 22M22 |
| 2021 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A![]() | Bjelica, Bogdan | Article | 22M22 |
| 2021 | Cerebral involvement and related aspects in myotonic dystrophy type 2![]() | Perić, Stojan Z. | Article | 21M21 |
| 2021 | Osnovi neurološkog pregleda![]() | Kostić, Vladimir | Text book | Mp. category will be shown later |
| 2021 | Long-term outcome in patients with myasthenia gravis![]() | Božović, Ivo | Conference Paper | Mp. category will be shown later |
| 2021 | Cognitive function assessment in patients with myotonic dystrophy type 2![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2020 | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A![]() | Bjelica, Bogdan | Article | 22M22 |
| 2020 | Prospective analysis of gait characteristics in chronic inflammatory demyelinating polyradiculoneuropathy![]() | Božović, Ivo | Article | 22M22 |
| 2020 | Genetic yield of the PMP22 deletion analysis in patients with compressive neuropathies![]() | Perić, Stojan Z | Conference Paper | Mp. category will be shown later |
| 2020 | 5-year prospective study of quality of life in patients with myotonic dystrophy type 2![]() | Palibrk, Aleksa; Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2020 | Oligoclonal bands in the cerebrospinal fluid of patients with Guillain-Barre syndrome![]() | Kalač, Aida; Basta, Ivana Z. | Conference Paper | Mp. category will be shown later |
| 2020 | Neurologija : za studente medicine![]() | Kostić, Vladimir
Kozić, Duško
| Text book | Mp. category will be shown later |
| 2020 | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A![]() | Bjelica, Bogdan | Conference Paper | Mp. category will be shown later |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies![]() | Ivanović, Vukan | Article | 21M21 |
| 2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies![]() | Maksić, Jasmina | Article | 23M23 |
| 2020 | Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD)![]() | Fatehi, F.; Okhovat, AA; Nilipour, Y.; Mroczek, M.; Straub, V.; Topf, A.; Palibrk, Aleksa; Perić, Stojan Z.
Nafissi, S.;
| Article | 21aM21a |
| 2019 | Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease![]() | Wood, Libby; ...; Perić, Stojan Z. | Other | Mp. category will be shown later |
| 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 |
| 2019 | Heart involvement in patients with myotonic dystrophy type 2![]() | Perić, Stojan | Article | 22M22 |
| 2019 | Age, origin and spreading of the myotonic dystrophy type 2 mutation throughout Europe![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
