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A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.
Perić S, Glumac JN, Töpf A, Savić-Pavićević D, Phillips L, Johnson K, Cassop-Thompson M, Xu L, Bertoli M, Lek M, MacArthur D, Brkušanin M, Milenković S, Rašić VM, Banko B, Maksimović R, Lochmüller H, Stojanović VR, Straub V. Perić S, et al. Among authors: stojanovic vr. Eur J Hum Genet. 2017 May;25(5):572-581. doi: 10.1038/ejhg.2017.16. Epub 2017 Mar 15. Eur J Hum Genet. 2017. PMID: 28295036 Free PMC article.
Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness.
Johnson K, Töpf A, Bertoli M, Phillips L, Claeys KG, Stojanovic VR, Perić S, Hahn A, Maddison P, Akay E, Bastian AE, Łusakowska A, Kostera-Pruszczyk A, Lek M, Xu L, MacArthur DG, Straub V. Johnson K, et al. Among authors: stojanovic vr. Orphanet J Rare Dis. 2017 Nov 17;12(1):173. doi: 10.1186/s13023-017-0722-1. Orphanet J Rare Dis. 2017. PMID: 29149851 Free PMC article.
Fatigue in myotonic dystrophy type 1: a seven-year prospective study.
Peric S, Bjelica B, Bozovic I, Pesovic J, Paunic T, Banovic M, Brkusanin M, Aleksic K, Basta I, Pavicevic DS, Stojanovic VR. Peric S, et al. Among authors: stojanovic vr. Acta Myol. 2019 Dec 1;38(4):239-244. eCollection 2019 Dec. Acta Myol. 2019. PMID: 31970322 Free PMC article.
Peripheral neuropathy in patients with myotonic dystrophy type 1.
Peric S, Stojanovic VR, Nikolic A, Kacar A, Basta I, Pavlovic S, Lavrnic D. Peric S, et al. Among authors: stojanovic vr. Neurol Res. 2013 May;35(4):331-5. doi: 10.1179/1743132812Y.0000000144. Epub 2013 Jan 10. Neurol Res. 2013. PMID: 23336676
26 results