Researchers
Marjanović, Ana
Results 61-80 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Morphological and genetic analysis of freshwater sponges in Serbia![]() | Anđus, Stefan | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia![]() | Perić, Stojan | Article | Mp. category will be shown later |
| 2019 | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R. | Conference Paper | Mp. category will be shown later |
| 2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade![]() | Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation![]() | Ivančević, Nikola | Article | 23M23 |
| 2019 | Genetski zasnovana terapija neurodegenerativnih bolesti![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | The influence of polymorphisms in COMT, DAT (SLC6A3), DRD2, and ANKK1 genes on the onset of complications of long-term use of levodopa in individuals with Parkinson’s disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: First experience![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer disease![]() | Andabaka, Marko | Conference Paper | Mp. category will be shown later |
| 2019 | First record of freshwater sponge Trochospongilla horrida Weltner, 1893 in Serbia - A morphological and genetic study![]() | Anđus, Stefan | Article | 21M21 |
| 2019 | Molecular genetic testing of Huntington’s disease and genetic counselling![]() | Mandić, Ratka; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Genetika amiotrofične lateralne skleroze![]() | Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2019 | KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous Malformation![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2018 | Features of the Serbian cohort of patients with calpainopathy![]() | Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2018 | HTERT promoter methylation and single nucleotide polymorphism (-245 T > C) affect renal cell carcinoma behavior in Serbian population![]() | Trifunović, Jovanka | Article | 23M23 |
