Researchers
Keckarević-Marković, Milica
Results 61-80 of 132
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2015 | Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin | Kecmanović, Miljana | Article | 21M21 |
| 2015 | PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy | Milić Rašić, Vedrana | Article | 21M21 |
| 2015 | Is it easy to recognize HINT1 neuropathy (oral presentation) | Milić Rašić, V.; Branković, V.; Mladenović, J.; Nikodinović, J.; Kosac, A.; Baets, J.; De Jonghe, P.; Jordanova, A.; Zimon, M.; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2015 | Population analysis of the European standard set (ESS) loci and SE33 locus in a Republic of Serbia | Jakovski Z; Keckarević, Dušan | Conference Paper | Mp. category will be shown later |
| 2015 | Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies | Mladenović, J.; Glumac, J. Nikodinović; Kosać, A.; Keckarević Marković, Milica | Conference Paper | 21M21 |
| 2014 | A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia![]() | Kecmanović, Miljana | Article | 23M23 |
| 2014 | Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 gene | Keckarević, Dušan | Conference Paper | Mp. category will be shown later |
| 2014 | PALM-LCM in sexual assault cases | Kecmanović, Miljana | Conference Paper | Mp. category will be shown later |
| 2014 | Elevated level of creatin phospho kinase in the blood of patients with peripheral polyneuropathies | Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2014 | Pseudodominant inheritance in HINT1 neuropathy | Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić Milica; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2014 | Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim origin | Kecmanović, Miljana | Conference Paper | Mp. category will be shown later |
| 2013 | Rabdomioliza kao dijagnostički i terapijski izazov kod hereditarne neuropatije sa kongenitalnom kataraktom i facijalnim dismorfizmom | Nikodinović Glumac J; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2013 | CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype? | Nikodinović Glumac J; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2013 | 4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder | Milic, Rasic V.; Nikodinovic, J.; Mladenovic, J.; De, Jonghe P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević Marković, Milica | Article | 21M21 |
| 2013 | Primena tritikalea u fermentacionim procesima kao doprinos održivom razvoju | Кецкаревић-Марковић, Милица | Doctoral theses | 70M70 |
| 2013 | Clinical and neurophysiologic charactersitics of HINT1 neuropathy in Serbian patients | Milić-Rasić, M.; Nikodinović, J.; Mladenović, J.; Jordanova, A.; Baets, J.; Zimon, M.; De Jonghe, P.; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2013 | Quality of life in patients with Charcot-Marie-Tooth disease in population of Belgrade | Jelena Mladenović; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2013 | Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicity | Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2013 | Clinical and Neurophysiologic characteristics of HINT1 neuropathy in Serbian patients | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
