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Author/Creator Iglseder, Stephan

1. Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study. (10th March 2022)

Authors:
Krenn, Martin; Tomschik, Matthias; Wagner, Matias; Zulehner, Gudrun; Weng, Rosa; Rath, Jakob; Klotz, Sigrid; Gelpi, Ellen; Bsteh, Gabriel; Keritam, Omar; Colonna, Isabella; Paternostro, Chiara; Jäger, Fiona; Lindeck‐Pozza, Elisabeth; Iglseder, Stephan; Grinzinger, Susanne; Schönfelder, Martina; H...
Journal:
European journal of neurology
Issue:
Volume 29:Number 6(2022)
Page Start:
1815
Record Type:
Journal Article
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3. Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1. Issue 6 (December 2013)

Authors:
Nilsson, Johanna; Schoser, Benedikt; Laforet, Pascal; Kalev, Ognian; Lindberg, Christopher; Romero, Norma B.; Dávila López, Marcela; Akman, Hasan O.; Wahbi, Karim; Iglseder, Stephan; Eggers, Christian; Engel, Andrew G.; DiMauro, Salvatore; Oldfors, Anders
Journal:
Annals of neurology
Issue:
Volume 74:Issue 6(2013:Dec.)
Page Start:
914
Record Type:
Journal Article
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4. The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME. (15th December 2020)

Authors:
Senderek, Jan; Lassuthova, Petra; Kabzińska, Dagmara; Abreu, Lisa; Baets, Jonathan; Beetz, Christian; Braathen, Geir J.; Brenner, David; Dalton, Joline; Dankwa, Lois; Deconinck, Tine; De Jonghe, Peter; Dräger, Bianca; Eggermann, Katja; Ellis, Melina; Fischer, Carina; Stojkovic, Tanya; Herrmann, D...
Journal:
Neurology
Issue:
Volume 95:Number 24(2020)
Page Start:
Record Type:
Journal Article
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