Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jelena Nikodinovic Glumac"'
Autor:
Stojan, Peric, Jelena, Stevanovic, Katherine, Johnson, Ana, Kosac, Marina, Peric, Marija, Brankovic, Ana, Marjanovic, Milena, Jankovic, Bojan, Banko, Sanja, Milenkovic, Milica, Durdic, Ivo, Bozovic, Jelena Nikodinovic, Glumac, Dragana, Lavrnic, Ruzica, Maksimovic, Vedrana, Milic-Rasic, Vidosava, Rakocevic-Stojanovic
Publikováno v:
Acta Myologica
Limb-girdle muscular dystrophy (LGMD) type 2A (calpainopathy) is an autosomal recessive disease caused by mutation in the CAPN3 gene. The aim of this study was to examine genetic and phenotypic features of Serbian patients with calpainopathy. The stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7841af5b59975fb4bab921555693fce6
https://pubmed.ncbi.nlm.nih.gov/31788660
https://pubmed.ncbi.nlm.nih.gov/31788660
Autor:
Peter Hackman, Bjarne Udd, Carsten G. Bönnemann, Ana Ferreiro, Carsten Bonnemann, Alan Beggs, Mathias Gautel, Mark Davis, Teresinha Evangelista, Marco Savarese, Jelena Nikodinovic Glumac, Jocelyn Laporte, John Edward Smith, Isabelle Richard, Henk Granzier, Raphäel Schneider, Heinz Jungbluth, Sarah Foye, Alison Rockett Frase
Publikováno v:
Neuromuscular Disorders
Neuromuscular Disorders, 2017, 27 (4), pp.396-407. ⟨10.1016/j.nmd.2017.01.009⟩
Neuromuscular Disorders, Elsevier, 2017, 27 (4), pp.396-407. ⟨10.1016/j.nmd.2017.01.009⟩
Neuromuscular Disorders, 2017, 27 (4), pp.396-407. ⟨10.1016/j.nmd.2017.01.009⟩
Neuromuscular Disorders, Elsevier, 2017, 27 (4), pp.396-407. ⟨10.1016/j.nmd.2017.01.009⟩
International audience; No abstract available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191c032eef75660635f52d2484fbcb37
https://hal.science/hal-02333059/document
https://hal.science/hal-02333059/document
Autor:
Albena Jordanova, David Blocquel, Derek Atkinson, Tinne Ooms, Thorsten Hornemann, Vedrana Milic Rasic, Xiang-Lei Yang, Biljana Ermanoska, Alejandro Estrada-Cuzcano, Regula Steiner, Jelena Nikodinovic Glumac, K. Peeters, Els De Vriendt, Bob Asselbergh
Publikováno v:
Neurology
Objective:To identify the unknown genetic cause in a nuclear family with an axonal form of peripheral neuropathy and atypical disease course.Methods:Detailed neurologic, electrophysiologic, and neuropathologic examinations of the patients were perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e5465acabedf6040aaf9ded4c41249
https://hdl.handle.net/10067/1421940151162165141
https://hdl.handle.net/10067/1421940151162165141
Autor:
Atkinson, Derek, Glumac, Jelena Nikodinovic, Asselbergh, Bob, Ermanoska, Biljana, Blocquel, David, Steiner, Regula, Estrada-Cuzcano, Alejandro, Peeters, Kristien, Ooms, Tinne, De Vriendt, Els, Xiang-Lei Yang, Hornemann, Thorsten, Milic Rasic, Vedrana, Jordanova, Albena, Nikodinovic Glumac, Jelena, Yang, Xiang-Lei
Publikováno v:
Neurology; 2/7/2017, Vol. 88 Issue 6, p533-542, 10p, 1 Color Photograph, 2 Charts, 2 Graphs