Autori: Marjanovic Ana
Naslov | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression (Meeting Abstract) |
Autori | Pesic Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 888-888 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy (Article) |
Autori | Dawod Phepy GA Jancic Jasna B ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | GENES, (2020), vol. 11 br. 9, str. - |
Projekat | Serbian Ministry of Education, Science and Technological Development [ON175090, ON175091, 200110] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | The influence of ANNK1/DRD2 haplotypes on the onset of complications of long-term levodopa therapy in Parkinson's disease (Meeting Abstract) |
Autori | Radojevic Branislava Dragasevic-Miskovic Natasa T Marjanovic Ana ![]() ![]() ![]() ![]() |
Info | MOVEMENT DISORDERS, (2020), vol. 35 br. , Suppl. 1, str. S473-S474 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Yield of thePMP22deletion analysis in patients with compression neuropathies (Article) |
Autori | Ivanovic Vukan Marjanovic Ana ![]() ![]() ![]() ![]() ![]() |
Info | JOURNAL OF NEUROLOGY, (2020), vol. 267 br. 12, str. 3617-3623 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (Article) |
Autori | Bjelica Bogdan Peric Stojan Z ![]() ![]() ![]() ![]() ![]() |
Info | NEUROLOGICAL SCIENCES, (2020), vol. 41 br. 3, str. 625-630 |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175083] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation (Article) |
Autori | Ivancevic Nikola ![]() ![]() ![]() ![]() ![]() ![]() |
Info | VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 5, str. 543-546 |
Projekat | Serbian Ministry of Education, Science and Technological Development [ON175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract) |
Autori | Marjanovic Ana ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | NOTCH3 mutations in Serbian CADASIL patients (Meeting Abstract) |
Autori | Jankovic Milena Z ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 293-293 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience (Meeting Abstract) |
Autori | Brankovic M Dobricic Valerija S Svetel Marina V ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 292-292 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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