Researchers
Dobričić, Valerija
Results 81-89 of 89
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2014 | Metabolic syndrome in patients with myotonic dystrophy type 1![]() | Vujnić, Milorad; Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2014 | Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depression disorder![]() | Canu, Elisa; Kostić, Milutin | Conference Paper | Mp. category will be shown later |
| 2014 | Splice site mutation in amelogenin X-linked gene, genotypephenotype relation![]() | Toljić, Boško M. | Conference Paper | Mp. category will be shown later |
| 2014 | Significant impact of behavioral and cognitive impairment on quality of life in patients with myotonic dystrophy type 1![]() | Stojanović-Rakočević, Vidosava | Article | 22M22 |
| 2014 | De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient![]() | Dobričić, Valerija | Article | 21aM21a |
| 2014 | Shorter CTG repeats length in an oligodendroglioma from a myotonic dystrophy type 1 patient![]() | Stojanović, Vidosava | Article | 23M23 |
| 2014 | Transcranial sonography in patients with myotonic dystrophy type 1![]() | Perić, Stojan | Article | 22M22 |
| 2011 | Direct detection of DMD/BMD carriers by quantitative real-time PCR![]() | Maksimović, Nela | Conference Paper | Mp. category will be shown later |
| 2007 | MECP2 mutations in Serbian Rett syndrome patients | Đarmati, Ana; Dobričić, Valerija | Article | 22M22 |
