Researchers
Milić-Rašić, Vedrana
Results 21-40 of 84
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | Genotype-phenotype correlation in Friedreich's ataxia![]() | Kovačević, G.; Todorović, S.; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2016 | Osnovi neurološkog pregleda![]() | Kostić, Vladimir | Text book | Mp. category will be shown later |
| 2016 | Treatment options in HINT1 neuropathy | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2016 | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats | Gagic, Milica; Keckarević Marković, Milica | Article | 21M21 |
| 2016 | Phenotypic characteristics of titinopathy caused by a founder autosomal recessive mutation in Serbian population | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2016 | A recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohort | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2016 | A novel recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohort | J. Nikodinović-Glumac; A. Topf; H. Lochmüller; Savić Pavićević, Dušanka Lj. | Conference Paper | Mp. category will be shown later |
| 2016 | Neurologija : za studente medicine![]() | Apostolski, Slobodan
Kozić, Duško
| Text book | Mp. category will be shown later |
| 2015 | Mreža za neuromišićne bolesti Srbije (NMD-SerbNet)![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Unapređenje genetičke dijagnostike spinalne mišićne atrofije primenom metode multipleks amplifikacije ligiranih proba | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Correlation of copy number of the SMN2, SERF1A and NAIP genes with severity of spinal muscular atrophy in Serbian patients | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy | Milić Rašić, Vedrana | Article | 21M21 |
| 2015 | Intellectual ability in the Duchenne muscular dystrophy and dystrophin gene mutation location![]() | Milić-Rašić, Vedrana | Article | 23M23 |
| 2015 | Single referral center study in Serbia: a case series of 41 patients with congenital myasthenic syndromes | Ana Kosać | Conference Paper | Mp. category will be shown later |
| 2015 | Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies | Mladenović, J.; Glumac, J. Nikodinović; Kosać, A.; Keckarević Marković, Milica | Conference Paper | 21M21 |
| 2015 | Joint effect of the SMN2 and SERF1A genes on early-onset Serbian spinal muscular atrophy patients | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Common features of the cerebral perforating arteries and their clinical significance![]() | Đulejić, Vuk | Article | 22M22 |
| 2015 | Genetip- fenotip korelacija kod spinalne mišićne atrofi je (SMA)![]() | Knežević-Pogančev, Marija | Article | 52M52 |
| 2014 | Intellectual ability in Duchenne muscular dystrophy and dystrophin gene mutation location | Vojinović D; Pešović, Jovan | Conference Paper | Mp. category will be shown later |
