Autori: Jankovic Milena Z
Naslov | Oligoclonal bands in the cerebrospinal fluid of patients with Guillain-Barre syndrome (Meeting Abstract) |
Autori | Kalac Aida Basta Ivana Z Bozovic Ivo Jankovic Milena Z Berisavac Iva I Palibrk Aleksa Stojiljkovic-Tamas Olivera Jovanovic Dejana R Stevic Zorica D Rakocevic-Stojanovic Vidosava M Lavrnic Dragana V Peric Stojan Z |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2020), vol. 27 br. , Suppl. 1, str. 948-948 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot-Marie-Tooth disease type 1A (Meeting Abstract) |
Autori | Bjelica Bogdan Peric Stojan Z Bozovic Ivo Basta Ivana Z Kacar Aleksandra S Jankovic Milena Z Brankovic Marija Palibrk Aleksa Novakovic Ivana V Lavrnic Dragana V Stevic Zorica D Rakocevic-Stojanovic Vidosava M |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2020), vol. 27 br. , Suppl. 1, str. 400-400 |
Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175083] |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (Article) |
Autori | Bjelica Bogdan Peric Stojan Z Basta Ivana Z Bozovic Ivo Kacar Aleksandra S Marjanovic Ana Ivanovic Vukan Marjanovic Ana Jankovic Milena Z Novakovic Ivana V Rakocevic-Stojanovic Vidosava M |
Info | NEUROLOGICAL SCIENCES, (2020), vol. 41 br. 3, str. 625-630 |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175083] |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy (Meeting Abstract) |
Autori | Dawod Phepy GA Rovcanin Branislav R Marjanovic Ana Marjanovic Ana Jankovic Milena Z Novakovic Ivana V Motaleb Abdel F Jancic Jasna B Kostic Vladimir S |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract) |
Autori | Marjanovic Ana Dobricic Valerija S Brankovic Marija Jankovic Milena Z Mandic Gorana B Stefanova Elka D Stevic Zorica D Novakovic Ivana V Kostic Vladimir S |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | NOTCH3 mutations in Serbian CADASIL patients (Meeting Abstract) |
Autori | Jankovic Milena Z Dobricic Valerija S Marjanovic Ana Brankovic Marija Pavlovic Aleksandra M Dujmovic Irena Mijajlovic Milija D Novakovic Ivana V Kostic Vladimir S |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 293-293 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (Meeting Abstract) |
Autori | Dawod Phepy GA Rovcanin Branislav R Marjanovic Ana Marjanovic Ana Jankovic Milena Z Novakovic Ivana V Dujmovic Irena Jancic Jasna B Kostic Vladimir S |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 181-181 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Body composition analysis in patients with myotonic dystrophy types 1 and 2 (Article) |
Autori | Peric Stojan Z Bozovic Ivo Nisic Tanja Banovic Marija Vujnic Milorad Svabic Tamara S Pesovic Jovan Brankovic Marija Basta Ivana Z Jankovic Milena Z Savic-Pavicevic Dusanka Lj Rakocevic-Stojanovic Vidosava M |
Info | NEUROLOGICAL SCIENCES, (2019), vol. 40 br. 5, str. 1035-1040 |
Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175083] |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract) |
Autori | Jankovic Milena Z Dobricic Valerija S Kresojevic Nikola D Markovic Vladana V Petrovic Igor N Svetel Marina V Pekmezovic Tatjana D Novakovic Ivana V Kostic Vladimir K |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract) |
Autori | Marjanovic Ana Dobricic Valerija S Marjanovic Ivan V Brankovic Marija Jankovic Milena Z Mandic Gorana B Stevic Zorica D Novakovic Ivana V Stefanova Elka D Kostic Vladimir K |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |