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Autori: Nikodinovic-Glumac Jelena

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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  
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