Autori: Nikodinovic Jelena
| 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 | Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia (Article) |
| Autori | Zimon Magdalena ... Nikodinovic Jelena ... Todorovic Slobodanka Savic-Pavicevic Dusanka Lj ... Milic-Rasic Vedrana M ... (broj koautora 37) |
| Info | NATURE GENETICS, (2012), vol. 44 br. 10, str. 1080-1083 |
| Projekat | University of Antwerp (in part by IWS BOF) [23064]; Fund for Scientific Research-Flanders; Medical Foundation Queen Elisabeth (GSKE); Interuniversity Attraction Poles program of the Belgian Federal Science Policy Office (BELSPO) [P6/43]; Methusalem Excell |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Clinical presentation in patients with congenital myasthenic syndrome (CMS) due to CHRNE mutations (Meeting Abstract) |
| Autori | Nikodinovic Jelena Milic-Rasic Vedrana M |
| Info | EUROPEAN JOURNAL OF NEUROLOGY, (2012), vol. 19 br. , Suppl. 1, str. 32-32 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
