eNauka - pregled
Pregled prema Autor Milić-Rašić, Vedrana
Prikaz rezultata 1 do 20 od 75
sledeće >
Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
---|---|---|---|---|
2008 | A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease | Keckarević-Marković, Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2016 | A novel recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohort | J. Nikodinović-Glumac; A. Topf; H. Lochmüller; Savić Pavićević, Dušanka Lj. ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population | Pešović, Jovan Z. ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2017 | A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population. (✓) | Perić, Stojan ![]() ![]() ![]() | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
2016 | A recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohort | Perić, Stojan ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 23M23 - Rad u međ. časopisu |
2013 | Analiza rearanžmana u genu za distrofin primenom metode multipleks amplifikacije ligiranih proba | Pešović, Jovan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2020 | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies (✓) | Maksić, Jasmina ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 23M23 - Rad u međ. časopisu |
2016 | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats | Gagic, Milica; Keckarević Marković, Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
2014 | Association of SMN2 gene copy number with clinical types of spinal muscular atrophy (SMA) in Serbian patients | Brkušanin, Miloš ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2010 | Autoimmune myasthenia gravis: the youngest patient diagnosed in Serbia | Milić-Rašić, Vedrana ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2012 | Cardiac assessment in boys with Duchenne muscular dystrophy | Dina Vojinović; Milić-Rašić, Vedrana ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2021 | Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3 (✓) | Đorđević, Stefan A.; Milić-Rasić, Vedrana M. ![]() ![]() ![]() ![]() | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
2013 | CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype? | Nikodinović Glumac J; Milić-Rašić, Vedrana ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2013 | Clinical and Neurophysiologic characteristics of HINT1 neuropathy in Serbian patients | Milić-Rašić, Vedrana ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2012 | Clinical presentation in patients with congenital myasthenic syndrome (CMS) due to CHRNE mutations | Milić-Rašić, Vedrana ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2015 | Common features of the cerebral perforating arteries and their clinical significance (✓) | Đulejić, Vuk ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
2012 | Community-based study of health-related quality of life in spinal cord injury, muscular dystrophy, multiple sclerosis, and cerebral palsy | Jovanović, Mirjana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
2010 | Comparison of Charcot-Marie-Tooth neuropathy type 2 and type 1A: clinical characteristics | Milić-Rašić, Vedrana ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2009 | Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients | Keckarević-Marković, Milica ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |