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Axial myopathy in parkinsonism.
Wanschitz JV, Sawires M, Seppi K, Boesch S, Loescher WN, Schocke M, Poewe W. Wanschitz JV, et al. Mov Disord. 2011 Jul;26(8):1569-71. doi: 10.1002/mds.23492. Epub 2011 Apr 25. Mov Disord. 2011. PMID: 21520279 No abstract available.
Hereditary transthyretin-related amyloidosis.
Finsterer J, Iglseder S, Wanschitz J, Topakian R, Löscher WN, Grisold W. Finsterer J, et al. Among authors: wanschitz j. Acta Neurol Scand. 2019 Feb;139(2):92-105. doi: 10.1111/ane.13035. Epub 2018 Oct 23. Acta Neurol Scand. 2019. PMID: 30295933
Hereditary ATTR Amyloidosis in Austria: Prevalence and Epidemiological Hot Spots.
Auer-Grumbach M, Rettl R, Ablasser K, Agis H, Beetz C, Duca F, Gattermeier M, Glaser F, Hacker M, Kain R, Kaufmann B, Kovacs GG, Lampl C, Ljevakovic N, Nagele J, Pölzl G, Quasthoff S, Raimann B, Rauschka H, Reiter C, Skrahina V, Schuhfried O, Sunder-Plassmann R, Verheyen ND, Wanschitz J, Weber T, Windhager R, Wurm R, Zimprich F, Löscher WN, Bonderman D. Auer-Grumbach M, et al. Among authors: wanschitz j. J Clin Med. 2020 Jul 14;9(7):2234. doi: 10.3390/jcm9072234. J Clin Med. 2020. PMID: 32674397 Free PMC article.
Hypoxia up-regulates the angiogenic cytokine secretoneurin via an HIF-1alpha- and basic FGF-dependent pathway in muscle cells.
Egger M, Schgoer W, Beer AG, Jeschke J, Leierer J, Theurl M, Frauscher S, Tepper OM, Niederwanger A, Ritsch A, Kearney M, Wanschitz J, Gurtner GC, Fischer-Colbrie R, Weiss G, Piza-Katzer H, Losordo DW, Patsch JR, Schratzberger P, Kirchmair R. Egger M, et al. Among authors: wanschitz j. FASEB J. 2007 Sep;21(11):2906-17. doi: 10.1096/fj.06-7440com. Epub 2007 May 15. FASEB J. 2007. PMID: 17504977
The prion protein in human neuromuscular diseases.
Kovács GG, Kalev O, Gelpi E, Haberler C, Wanschitz J, Strohschneider M, Molnár MJ, László L, Budka H. Kovács GG, et al. Among authors: wanschitz j. J Pathol. 2004 Nov;204(3):241-7. doi: 10.1002/path.1633. J Pathol. 2004. PMID: 15476279
91 results