Autori: Jankovic Milena Z
Naslov | Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (Article) |
Autori | Hsu Sandy Chan ... Dobricic Valerija S ... Jankovic Milena Z ... Kostic Vladimir S ... Novakovic Ivana V ... (broj koautora 52) |
Info | NEUROGENETICS, (2013), vol. 14 br. 1, str. 11-22 |
Projekat | NIH/NINDS [R01 NS040752]; CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico); CAPES (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior to JRMO); FAPESP/CEPID (State of Sao Paulo Research Foundation to MZ); FACEPE (Fundacao de A |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Genetic testing in familial and young-onset Alzheimer's disease: mutation spectrum in a Serbian cohort (Article) |
Autori | Dobricic Valerija S Stefanova Elka D Jankovic Milena Z Gurunlian Nicole Novakovic Ivana V Hardy John Kostic Vladimir S Guerreiro Rita |
Info | NEUROBIOLOGY OF AGING, (2012), vol. 33 br. 7, str. - |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |