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Преглед према Аутор Dobricic, Valerija
Приказ резултата 1 до 10 од 10
| 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  ; Djuric, Gordana; Novaković, Ivana  ; Dobricic, Valerija; Stefanova, Elka ; Kresojevic, Nikola ; Tomić, Aleksandra ; Jankovic, Milena ; Petrović, Igor ; Pekmezović, Tatjana ;
Kostić, Vladimir
; | Научни чланак | 23M23 - Међународни часопис категорије M23 |
| 2013 | Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilsons disease in Serbia | Tomić, Aleksandra ; Dobricic, Valerija; Novaković, Ivana ; Svetel, Marina ; Pekmezović, Tatjana ; Kresojevic, Nikola ; Potrebic, Aleksandra; Kostić, Vladimir | Научни чланак | 23M23 - Међународни часопис категорије M23 |
| 2012 | Could Spindle Cell Lung Carcinoma be Considered and Treated as Sarcoma, According to its Clinical Course, Morphology, Immunophenotype and Genetic Finding? | Kontić, Milica ; Stojsic, Jelena; Stević, Ruža ; Bunjevački, Vera ; Jekić, Biljana ; Dobricic, Valerija | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2016 | Excellent outcome of pallidal deep brain stimulation in DYT6 dystonia: A case report | Vuletic, Vladimira; Chudy, Darko; Almahariq, Fadi; Dobricic, Valerija; Kostić, Vladimir ; Bogdanovic, Nenad | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2012 | Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort | Dobricic, Valerija; Stefanova, Elka ; Jankovic, Milena ; Gurunlian, Nicole; Novaković, Ivana ; Hardy, John; Kostić, Vladimir ; Guerreiro, Rita | Научни чланак | 21a+M21a+ - Водећи међународни часопис категорије M21a+ |
| 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;
Gillessen-Kaesbach, Gabriele; Westenberger, Ana; Savić Pavićević, Dušanka
; Münchau, Alexander; Oprea, Gabriela; Klein, Christine; Rolfs, Arndt; Martemyanov, Kirill A.; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 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
; Kostić, Vladimir; Dobricic, Valerija; Lohmann, Ebba; Hanagasi, Hasmet; Guven, Gamze; Bilgic, Basar; Bras, Jose; Guerreiro, Rita; Beule, Dieter; Dirnagl, Ulrich; Sassi, Celeste; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2016 | The cumulative effect of genetic polymorphisms on depression and brain structural integrity | Kostić, Milutin ; Canu, Elisa; Agosta, Federica; Munjiza, Ana; Novaković, Ivana ; Dobricic, Valerija; Maria, Ferraro Pilar; Miler, Jerkovic Vera ; Pekmezović, Tatjana ; Lecic, Tosevski Dusica;
Filippi, Massimo;
| Article | 21a+M21a+ |
| 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
; Kostic, Vladimir; Dobricic, Valerija; Lohmann, Ebba; Hanagasi, Hasmet; Santos, Mariana; Guven, Gamze; Bilgic, Basar; Bras, Jose; Beule, Dieter; Dirnagl, Ulrich; Guerreiro, Rita; Sassi, Celeste; | Article | 21M21 |
| 2007 | Unverricht-Lundborg disease - the first report of genetically confirmed case in Serbia | Kecmanović, Miljana M. ; Ercegovac, Maja ; Dimitrijević, Rajko ; Dobricic, Valerija; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Sarić, M.; Bumbaširević, Ljiljana ; Romac, Stanka | Conference Paper | Mp. category will be shown later |