Autori: Jankovic Milena Z
Naslov | Presenting symptoms of GBA-related Parkinson's disease (Article) |
Autori | Kresojevic Nikola D Jankovic Milena Z Petrovic Igor N Kumar Kishore R Dragasevic Natasa T Dobricic Valerija S Novakovic Ivana V Svetel Marina V Klein Christine Pekmezovic Tatjana D Kostic Vladimir S |
Info | PARKINSONISM & RELATED DISORDERS, (2015), vol. 21 br. 7, str. 804-807 |
Projekat | Ministry of Education and Science, Republic of Serbia [ON175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Presenting symptoms of GBA-related Parkinson's disease (Meeting Abstract) |
Autori | Kresojevic Nikola D Jankovic Milena Z Petrovic Igor N Kumar Kishore R Dragasevic Natasa T Dobricic Valerija S Novakovic Ivana V Svetel Marina V Klein Christine Pekmezovic Tatjana D Kostic Vladimir K |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2015), vol. 22 br. , Suppl. 1, str. 437-437 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Identification of novel mutations in LRRK2 gene in patients with Parkinson's disease (Meeting Abstract) |
Autori | Jankovic Milena Z Kresojevic Nikola D Dobricic Valerija S Markovic Vladana V Petrovic Igor N Novakovic Ivana V Kostic Vladimir S |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2015), vol. 22 br. , Suppl. 1, str. 354-354 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population (Article) |
Autori | Jankovic Milena Z Kresojevic Nikola D Dobricic Valerija S Markovic Vladana V Petrovic Igor N Novakovic Ivana V Kostic Vladimir S |
Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2015), vol. 353 br. 1-2, str. 59-62 |
Projekat | Science of Republic of Serbia [ON175090, ON175091]; Ministry of Education |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Transcranial brain parenchyma sonography in Parkinson's disease with glucocerebrosidase mutations (Meeting Abstract) |
Autori | Mijajlovic Milija D Kresojevic Nikola D Peric Stojan Z Pavlovic Aleksandra M Svetel Marina V Jankovic Milena Z Dobricic Valerija S Novakovic Ivana V Lakocevic Milan B Kostic Vladimir S |
Info | CEREBROVASCULAR DISEASES, (2013), vol. 35 br. , Suppl. 2, str. 59-59 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia (Article) |
Autori | Svetel Marina V Djuric Gordana M Novakovic Ivana V Dobricic Valerija S Stefanova Elka D Kresojevic Nikola D Tomic Aleksandra D Jankovic Milena Z Petrovic Igor N Pekmezovic Tatjana D Kostic Vladimir S |
Info | ACTA NEUROLOGICA BELGICA, (2013), vol. 113 br. 3, str. 243-245 |
Projekat | Ministry of Education and Science of the Republic of Serbia [175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations (Article) |
Autori | Kresojevic Nikola D Mijajlovic Milija D Peric Stojan Z Pavlovic Aleksandra M Svetel Marina V Jankovic Milena Z Dobricic Valerija S Novakovic Ivana V Lakocevic Milan B Klein Christine Kostic Vladimir S |
Info | PARKINSONISM & RELATED DISORDERS, (2013), vol. 19 br. 4, str. 431-435 |
Projekat | Ministry of Science and Technology (MST), Republic of Serbia [175090] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia (Article) |
Autori | Dobricic Valerija S Kresojevic Nikola D Svetel Marina V Jankovic Milena Z Petrovic Igor N Tomic Aleksandra D Novakovic Ivana V Kostic Vladimir S |
Info | JOURNAL OF NEUROLOGY, (2013), vol. 260 br. 4, str. 1037-1042 |
Projekat | Ministry of Education and Science, Republic of Serbia [ON175090, ON175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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