еНаука - преглед
Преглед према Аутор Dobricic, Valerija
Приказ резултата 1 до 15 од 15
Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
---|---|---|---|---|
2013 | A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia | Svetel, Marina ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2013 | Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilsons disease in Serbia | Tomić, Aleksandra ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2012 | Could Spindle Cell Lung Carcinoma be Considered and Treated as Sarcoma, According to its Clinical Course, Morphology, Immunophenotype and Genetic Finding? | Kontić, Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2016 | Excellent outcome of pallidal deep brain stimulation in DYT6 dystonia: A case report | Vuletic, Vladimira; Chudy, Darko; Almahariq, Fadi; Dobricic, Valerija; Kostić, Vladimir ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2014 | Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2 | Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2012 | Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort | Dobricic, Valerija; Stefanova, Elka ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2015 | Metabolic syndrome in patients with myotonic dystrophy type 1 | Vujnic, Milorad; Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2017 | Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans | Lohmann, Katja; Masuho, Ikuo; Patil, Dipak N.; Baumann, Hauke; Hebert, Eva; Steinrücke, Sofia; Trujillano, Daniel; Skamangas, Nickolas K.; Dobricic, Valerija; Hüning, Irina; | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2021 | PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice | Messerschmidt, Clemens; Foddis, Marco; Blumenau, Sonja; Müller, Susanne; Bentele, Kajetan; Holtgrewe, Manuel; Kun-Rodrigues, Celia; Alonso, Isabel; do Carmo Macario, Maria; Morgadinho, Ana Sofia;
Velon, Ana Graça; Santo, Gustavo; Santana, Isabel; Mönkäre, Saana; Kuuluvainen, Liina; Schleutker, Johanna; Pöyhönen, Minna; Myllykangas, Liisa; Senatore, Assunta; Berchtold, Daniel; Winek, Katarzyna; Meisel, Andreas; Pavlović, Aleksandra
![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2015 | Screening for <b><i>C9orf72</i></b> Expansion Mutation in Serbian Patients with Early-Onset Dementia | Mandić-Stojimenović, Gorana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2016 | The cumulative effect of genetic polymorphisms on depression and brain structural integrity![]() | Kostić, Milutin ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]()
Filippi, Massimo;
| Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |
2014 | Transcranial sonography in patients with myotonic dystrophy type 1 | Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2023 | TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients | Foddis, Marco; Blumenau, Sonja; Holtgrewe, Manuel; Paquette, Kimberly; Westra, Kaitlyn; Alonso, Isabel; Macario, Maria do Carmo; Morgadinho, Ana Sofia; Velon, Ana Graça; Santo, Gustavo;
Santana, Isabel; Mönkäre, Saana; Kuuluvainen, Liina; Schleutker, Johanna; Pöyhönen, Minna; Myllykangas, Liisa; Pavlović, Aleksandra
![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2007 | Unverricht-Lundborg disease - the first report of genetically confirmed case in Serbia | Kecmanović, Miljana M. ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
2015 | Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry | Stojanović, Vidosava ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |