Researchers
Brkušanin, Miloš
Results 101-120 of 120
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2015 | Varijantni ponovci kao mogući genetiĉki modifikatori DM1 | Pešović, Jovan | Conference Paper | 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 | Varijantni ponovci kao mogući genetički modifikatori DM1![]() | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2015 | Variant repeats in DM1 patients might be associated with milder clinical presentation![]() | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2015 | Pacijenti sa miotoničnom distrofijom tip 2 iz Srbije nose evropske osnivačke haplotipove![]() | Kovčić, Vlado; Stojanović, Vidosava | Conference Paper | Mp. category will be shown later |
| 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 | 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 | European founder haplotypes in Serbian patients with myotonic dystrophy type 2 | Kovčić Vlado; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2015 | (Beograd): Unapređenje genetiĉke dijagnostike spinalne mišićne atrofije primenom metode multipleks amplifikacije ligiranih proba | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients | Brkusanin, Milos | Article | 22M22 |
| 2015 | Pacijenti sa miotoniĉnom distrofijom tip 2 iz Srbije nose evropske osnivaĉke haplotipove | Kovčić, V.; Rakoĉević-Stojanović, V.; Perić, S.; Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2014 | NMD SerbNet - integrativni pristup u dijagnostici neuromišićnih bolesti u Srbiji![]() | Milić-Rašić, Vedrana | Article | 52M52 |
| 2014 | Repeat-primed PCR in diagnostic testing of repeat expansion diseases | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2014 | PCR based Southern blot method for detection of expansions associated with myotonic dystrophy type 2 | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2014 | Interactions of TPH2 variants and childhood abuse as risk factors for suicide attempt in Serbian psychiatric patients | Karanović, Jelena | Conference Paper | Mp. category will be shown later |
| 2014 | Diagnosis of neuromuscular diseases in Serbia and launch of the Serbian neuromuscular disease network NMD-SERBNET | Kojić, Snežana | Conference Paper | Mp. category will be shown later |
| 2014 | Association of SMN2 gene copy number with clinical types of spinal muscular atrophy (SMA) in Serbian patients | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2013 | From genotype to phenotype: in silico modelling of serotonergic system | Saša Šviković; Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2013 | Molecular genetics and genetic testing in myotonic dystrophy type 1 | Savić Pavićević, Dušanka | Article | 23M23 |
