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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2007 1
2008 1
2009 2
2010 3
2011 1
2012 1
2013 3
2014 3
2015 7
2016 4
2017 7
2018 4
2019 3
2020 4
2021 3
2022 6
2023 1
2024 4

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Page 1
Cognitive assessment in patients with myotonic dystrophy type 2.
Peric S, Gunjic I, Delic N, Stojiljkovic Tamas O, Salak-Djokic B, Pesovic J, Petrovic Djordjevic I, Ivanovic V, Savic-Pavicevic D, Meola G, Rakocevic-Stojanovic V. Peric S, et al. Among authors: savic pavicevic d. Neuromuscul Disord. 2022 Sep;32(9):743-748. doi: 10.1016/j.nmd.2022.06.011. Epub 2022 Jun 30. Neuromuscul Disord. 2022. PMID: 35879188 Free article.
Molecular genetics and genetic testing in myotonic dystrophy type 1.
Savić Pavićević D, Miladinović J, Brkušanin M, Šviković S, Djurica S, Brajušković G, Romac S. Savić Pavićević D, et al. Biomed Res Int. 2013;2013:391821. doi: 10.1155/2013/391821. Epub 2013 Mar 18. Biomed Res Int. 2013. PMID: 23586035 Free PMC article. Review.
Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2.
Peric S, Zlatar J, Nikolic L, Ivanovic V, Pesovic J, Petrovic Djordjevic I, Sreckovic S, Savic-Pavicevic D, Meola G, Rakocevic-Stojanovic V. Peric S, et al. Among authors: savic pavicevic d. Front Neurol. 2022 Jul 18;13:932883. doi: 10.3389/fneur.2022.932883. eCollection 2022. Front Neurol. 2022. PMID: 35923829 Free PMC article.
Clinical score for early diagnosis of myotonic dystrophy type 2.
Ivanovic V, Peric S, Pesovic J, Tubic R, Bozovic I, Petrovic Djordjevic I, Savic-Pavicevic D, Meola G, Rakocevic-Stojanovic V. Ivanovic V, et al. Among authors: savic pavicevic d. Neurol Sci. 2023 Mar;44(3):1059-1067. doi: 10.1007/s10072-022-06507-9. Epub 2022 Nov 19. Neurol Sci. 2023. PMID: 36401657 Free PMC article.
Multidimensional aspects of pain in myotonic dystrophies.
Peric M, Peric S, Rapajic N, Dobricic V, Savic-Pavicevic D, Nesic I, Radojicic S, Novakovic I, Lavrnic D, Rakocevic-Stojanovic V. Peric M, et al. Among authors: savic pavicevic d. Acta Myol. 2015 Dec;34(2-3):126-32. Acta Myol. 2015. PMID: 27199540 Free PMC article.
WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype.
Kulikovskaja L, Sarajlija A, Savic-Pavicevic D, Dobricic V, Klein C, Westenberger A. Kulikovskaja L, et al. Among authors: savic pavicevic d. Neurol Genet. 2018 Mar 27;4(2):e227. doi: 10.1212/NXG.0000000000000227. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29600274 Free PMC article. No abstract available.
50 results