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The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study.
Krenn M, Sener M, Rath J, Zulehner G, Keritam O, Wagner M, Laccone F, Iglseder S, Marte S, Baumgartner M, Eisenkölbl A, Liechtenstein C, Rudnik S, Quasthoff S, Grinzinger S, Spenger J, Wortmann SB, Löscher WN, Zimprich F, Kellersmann A, Rappold M, Bernert G, Freilinger M, Cetin H. Krenn M, et al. Among authors: loscher wn. J Neurol. 2023 Feb;270(2):909-916. doi: 10.1007/s00415-022-11440-0. Epub 2022 Oct 29. J Neurol. 2023. PMID: 36308527 Free PMC article.
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.
Fischer C, Trajanoski S, Papić L, Windpassinger C, Bernert G, Freilinger M, Schabhüttl M, Arslan-Kirchner M, Javaher-Haghighi P, Plecko B, Senderek J, Rauscher C, Löscher WN, Pieber TR, Janecke AR, Auer-Grumbach M. Fischer C, et al. Among authors: loscher wn. J Neurol. 2012 Mar;259(3):515-23. doi: 10.1007/s00415-011-6213-8. Epub 2011 Sep 4. J Neurol. 2012. PMID: 21892769 Free PMC article.
Hirayama disease in Austria.
Finsterer J, Löscher W, Wanschitz J, Baumann M, Quasthoff S, Grisold W. Finsterer J, et al. Joint Bone Spine. 2013 Oct;80(5):503-7. doi: 10.1016/j.jbspin.2012.10.013. Epub 2012 Dec 10. Joint Bone Spine. 2013. PMID: 23237996
Iatrogenic lesions of peripheral nerves.
Löscher WN, Wanschitz J, Iglseder S, Vass A, Grinzinger S, Pöschl P, Grisold W, Ninkovic M, Antoniadis G, Pedro MT, König R, Quasthoff S, Oder W, Finsterer J. Löscher WN, et al. Acta Neurol Scand. 2015 Nov;132(5):291-303. doi: 10.1111/ane.12407. Epub 2015 Apr 16. Acta Neurol Scand. 2015. PMID: 25882317 Review.
Secondary myopathy due to systemic diseases.
Finsterer J, Löscher WN, Wanschitz J, Quasthoff S, Grisold W. Finsterer J, et al. Among authors: loscher wn. Acta Neurol Scand. 2016 Dec;134(6):388-402. doi: 10.1111/ane.12576. Epub 2016 Feb 25. Acta Neurol Scand. 2016. PMID: 26915593 Free PMC article. Review.
124 results