Autori: Milic-Rasic Vedrana M
| Naslov | Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies (Article) |
| Autori | Maksic Jasmina Dobricic Valerija S Rasulic Lukas G Maksimovic Nela S Brankovic Marija Milic-Rasic Vedrana M Rakocevic-Stojanovic Vidosava M Novakovic Ivana V |
| Info | VOJNOSANITETSKI PREGLED, (2020), vol. 77 br. 4, str. 387-394 |
| Projekat | Serbian Ministry of Education, Science and Technological Development [175083, 175091] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article) |
| Autori | Dobricic Valerija S Tomic Aleksandra D Brankovic Vesna Kresojevic Nikola D Jankovic Milena Z Westenberger Ana Milic-Rasic Vedrana M Klein Christine Novakovic Ivana V Svetel Marina V Kostic Vladimir S |
| Info | PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84 |
| Projekat | Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population (Article) |
| Autori | Peric Stojan Z Nikodinovic-Glumac Jelena ... Savic-Pavicevic Dusanka Lj ... Brkusanin Milos Milenkovic Sanja M Milic-Rasic Vedrana M Banko Bojan Maksimovic Ruzica M ... Rakocevic-Stojanovic Vidosava M (broj koautora 19) |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2017), vol. 25 br. 5, str. 572-581 |
| Projekat | Sanofi Genzyme; Ultragenyx Pharmaceutical; LGMD2I Research Fund; Kurt+Peter Foundation; LGMD2D Foundation; Samantha J Brazzo Foundation; Medical Research Council UK [G1002274, 98482]; European Union [305444, 305121]; Ministry of Education, Science and Tec |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy (Article) |
| Autori | Atkinson Derek Nikodinovic-Glumac Jelena Asselbergh Bob Ermanoska Biljana Blocquel David Steiner Regula Estrada-Cuzcano Alejandro Peeters Kristien Ooms Tinne De Vriendt Els Yang Xiang-Lei Hornemann Thorsten Milic-Rasic Vedrana M Jordanova Albena |
| Info | NEUROLOGY, (2017), vol. 88 br. 6, str. 533-542 |
| Projekat | University of Antwerp [TOP BOF 29069]; Fund for Scientific Research-Flanders (FWO) [G.0543.13, G0D7713N]; Belgian Association against Neuromuscular Disorders (ABMM); NIH [NS 085092]; Fund for Scientific Research-Flanders |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Treatment options in HINT1 neuropathy (Meeting Abstract) |
| Autori | Nikodinovic-Glumac Jelena Milic-Rasic Vedrana M Brankovic Vesna Mladenovic Jelena M Todorovic Slobodanka |
| Info | EUROPEAN JOURNAL OF NEUROLOGY, (2016), vol. 23 br. , Suppl. 2, str. 470-470 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Compound Heterozygous Mutation in SGPL1 Causes Autosomal Recessive Charcot-Marie-Tooth Disease Type 2 in a Serbian Family (Meeting Abstract) |
| Autori | Atkinson Derek Asselbergs B De Vriendt Els Ooms T Estrada-Cuzcano A Nikodinovic Jelena Milic-Rasic Vedrana M Jordanova Albena |
| Info | JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, (2016), vol. 21 br. 3, str. 233-233 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats (Article) |
| Autori | Gagic Milica Keckarevic-Markovic Milica Kecmanovic Miljana Keckarevic Dusan P Mladenovic Jelena M Dackovic Jelena Milic-Rasic Vedrana M Romac Stanka P |
| Info | CLINICAL CHEMISTRY AND LABORATORY MEDICINE, (2016), vol. 54 br. 5, str. 773-780 |
| Projekat | Serbian Ministry of Education and Science [173016] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients (Article) |
| Autori | Brkusanin Milos Kosac Ana P Jovanovic Vladimir M Pesovic Jovan Brajuskovic Goran N Dimitrijevic Nikola Todorovic Slobodanka Romac Stanka P Milic-Rasic Vedrana M Savic-Pavicevic Dusanka Lj |
| Info | JOURNAL OF HUMAN GENETICS, (2015), vol. 60 br. 11, str. 723-728 |
| Projekat | Ministry of Education, Science and Technological Development, Republic of Serbia [173016] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Single referral center study in Serbia: a case series of 41 patients with congenital myasthenic syndromes (Meeting Abstract) |
| Autori | Kosac Ana P Milic-Rasic Vedrana M Mladenovic Jelena M Todorovic Slobodanka Vlahovic Gordana Rakocevic-Stojanovic Vidosava M Savic-Pavicevic Dusanka Lj Lochmuller H |
| Info | EUROPEAN JOURNAL OF NEUROLOGY, (2015), vol. 22 br. , Suppl. 1, str. 403-403 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations (Article) |
| Autori | Bladen Catherine L ... Monges Soledad Milic-Rasic Vedrana M Vojinovic Dina ... (broj koautora 61) |
| Info | HUMAN MUTATION, (2015), vol. 36 br. 4, str. 395-402 |
| Projekat | TREAT-NMD [FP6LSHM-CT-2006-036825, 20123307 UNEW_FY2013, AFM 16104]; European Union [305444, 305121] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
