еНаука - преглед
Преглед према Аутор Dobričić, Valerija
Приказ резултата 1 до 16 од 16
| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 2014 | C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome | Kostić, Vladimir  ; Dobričić, Valerija; Stanković, Iva; Ralić, Vesna; Stefanova, Elka | Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2011 | Epilepsy in a child with Wolf-Hirschhorn syndrome | Mitić, Vesna; Čuturilo, Goran  ; Novaković, Ivana ; Dimitrijević, Nikola; Damnjanović, Tatjana ; Dimitrijević, Aleksandar ; Dobričić, Valerija; Kostić, Vladimir ; Radlović, Nedeljko | Научни чланак | 23M23 - Међународни часопис категорије M23 |
| 2011 | Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification | Kostić, Vladimir ; Lukić-Ječmenica, Milica ; Novaković, Ivana ; Dobričić, Valerija; Brajković, Lela; Krajinović, Maja; Klein, Christine; Pavlović, Aleksandra | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2008 | HD phenocopies - Possible role of saitohin gene | Janković, N.; Kemanović, M. ; Dimitrijević, Rajna ; Keckarević-Marković, Milica ; Dobričić, Valerija; Savić-Pavićević, Dušanka ; Keckarević, D. ; Romac, Stanka | Naučni članak | 23M23 - Međunarodni časopis kategorije M23 |
| 2007 | Human Y-specific STR haplotypes in population of Serbia and Montenegro | Stevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2008 | Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population | Kecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Dobričić, Valerija; Keckarević, Dušan ; Ignjatović, P.; Romac, Stanka | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2014 | Mutations in Niemann Pick type C gene are risk factor for Alzheimer's disease | Kresojević, Nikola ; Dobričić, Valerija; Svetel, Marina ; Kostić, Vladimir | Naučni članak | 23M23 - Međunarodni časopis kategorije M23 |
| 2013 | Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice | Keller, Annika; Westenberger, Ana; Sobrido, Maria J; García-Murias, Maria; Domingo, Aloysius; Sears, Renee L; Lemos, Roberta R; Ordoñez-Ugalde, Andres; Nicolas, Gael; da, Cunha José E Gomes;
Rushing, Elisabeth J; Hugelshofer, Michael; Wurnig, Moritz C; Kaech, Andres; Reimann, Regina; Lohmann, Katja; Dobričić, Valerija; Carracedo, Angel; Petrović, Igor
; Miyasaki, Janis M; Abakumova, Irina; Mäe, Maarja Andaloussi; Raschperger, Elisabeth; Zatz, Mayana; Zschiedrich, Katja; Klepper, Jörg; Spiteri, Elizabeth; Prieto, Jose M; Navas, Inmaculada; Preuss, Michael; Dering, Carmen; Janković, Milena; Paucar, Martin; Svenningsson, Per; Saliminejad, Kioomars; Khorshid, Hamid R K; Novaković, Ivana; Aguzzi, Adriano; Boss, Andreas; Le, Ber Isabelle; Defer, Gilles; Hannequin, Didier; Kostić, Vladimir ; Campion, Dominique; Geschwind, Daniel H; Coppola, Giovanni; Betsholtz, Christer; Klein, Christine; Oliveira, Joao R M; | Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
| 2014 | Neurogenetika u eri 'omika' | Novaković, Ivana ; Dobričić, Valerija; Janković, Milena; Petrović, Igor; Stefanova, Elka; Svetel, Marina ; Kostić, Vladimir | Book parts | Mp. category will be shown later |
| 2013 | No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease | Svetel, Marina ; Pekmezović, Tatjana ; Marković, Vladana ; Novaković, Ivana ; Dobričić, Valerija; Djuric, Gordana; Stefanova, Elka ; Kostić, Vladimir | Article | 22M22 |
| 2011 | NPM1 gene mutations in children with Myelodysplastic syndromes | Jekić, Biljana ; Bunjevački, Vera ; Dobričić, Valerija; Novaković, Ivana ; Milašin, Jelena ; Popović, Branka ; Damnjanović, Tatjana ; Maksimović, Nela ; Perović, V. ; Luković, Ljiljana | Article | 23M23 |
| 2018 | Phenotype of PLP1-related Disorder Caused by Novel Mutation: A Case Report | Kresojević, Nikola; Petrović, Igor; Dobričić, Valerija; Tomić, Aleksandra; Branković, Vesna; Milić Rašić, Vedrana ; Svetel, Marina; Kostić, Vladimir | Article | Mp. category will be shown later |
| 2010 | Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population | Dimitrijević, Rajna ; Cadez, Ivana; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić-Pavićević, Dušanka ; Brajusković, Goran ; Romac, Stanka | Article | 23M23 |
| 2011 | Retinoic acid induced 1 gene and clinical subtypes of schizophrenia: An association study | Ivković, Maja ; Zamurović, Ljubica; Jovanović, Aleksandar; Dobričić, Valerija; Damjanović, Aleksandar ; Savić Pavićević, Dušanka ; Romac, Stanka | Article | 21M21 |
| 2010 | Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population | Kecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna ; Keckarević, Dušan ; Savić-Pavićević, Dušanka ; Keckarević-Marković, Milica ; Ivković, Maja ; Romac, Stanka | Article | 23M23 |
| 2013 | Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations | Kresojević, Nikola ; Mijajlović, Milija ; Perić, Stojan ; Pavlović, Aleksandra ; Svetel, Marina ; Janković, Milena ; Dobričić, Valerija; Novaković, Ivana ; Lakočević, Milan B.; Klein, Christine;
Kostić, Vladimir
; | Article | 21M21 |