Autori: Nikodinovic-Glumac Jelena
Naslov | The international database of titin gene variations and their phenotypes (Meeting Abstract) |
Autori | Hackman P Savarese M Bonnemann C Ferreiro A Beggs A Dawson Jesse Thompson R Evangelista T Lochmuller H Nikodinovic-Glumac Jelena Jungbluth H Foye S Udd B |
Info | NEUROMUSCULAR DISORDERS, (2018), vol. 28 br. , Suppl. 2, str. S104-S104 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Establishment of an international database of Titin mutations and their phenotypes - a follow up (Meeting Abstract) |
Autori | Hackman P ... Nikodinovic-Glumac Jelena ... (broj koautora 18) |
Info | NEUROMUSCULAR DISORDERS, (2017), vol. 27 br. , Suppl. 2, str. S239-S240 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
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 | A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohort (Meeting Abstract) |
Autori | Tonf A Nikodinovic-Glumac Jelena Peric Stojan Z Cassop-Thompson M Bertoli M Johnson Katherine Phillips L MacArthur D Rakocevic-Stojanovic Vidosava M Straub V |
Info | NEUROMUSCULAR DISORDERS, (2016), vol. 26 br. , Suppl. 2, str. S113-S114 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |