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Autori: Jankovic Milena Z

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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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