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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  
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