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Julia Wanschitz

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G Bsteh; H Gruber; Klaus Seppi; Julia Wanschitz; W N Löscher
Prognosis and prognostic factors in non-traumatic acute-onset compressive mononeuropathies - radial and peroneal mononeuropathies.
Wolfgang N Löscher; Monika Wallnöfer; Julia Wanschitz; Alexander Woertz; Gerhard Luef
Successful treatment of CANOMAD with IVIg and rituximab.
Wolfgang Nachbauer; Werner Poewe; Markus Reindl; Sylvia Boesch; Andreas Eigentler; Kurt Hufler; Wolfgang Löscher; Julia Wanschitz
Skeletal muscle involvement in friedreich ataxia and potential effects of recombinant human erythropoietin administration on muscle regeneration and neovascularization.

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All Publications

2013: G Bsteh; H Gruber; Klaus Seppi; Julia Wanschitz; W N Löscher
Prognosis and prognostic factors in non-traumatic acute-onset compressive mononeuropathies - radial and peroneal mononeuropathies.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013;20(6):981-5.
2013: Wolfgang N Löscher; Monika Wallnöfer; Julia Wanschitz; Alexander Woertz; Gerhard Luef
Successful treatment of CANOMAD with IVIg and rituximab.
Journal of neurology 2013;260(4):1168-70.
2012: Wolfgang Nachbauer; Werner Poewe; Markus Reindl; Sylvia Boesch; Andreas Eigentler; Kurt Hufler; Wolfgang Löscher; Julia Wanschitz
Skeletal muscle involvement in friedreich ataxia and potential effects of recombinant human erythropoietin administration on muscle regeneration and neovascularization.
Journal of neuropathology and experimental neurology 2012;71(8):708-15.
2012: Josef Finsterer; Wolfgang Löscher; Stefan Quasthoff; Michaela Auer-Grumbach; Julia Wanschitz; Giovanni Stevanin
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
Journal of the neurological sciences 2012;318(1-2):1-18.
2011: Julia Wanschitz; Sylvia Boesch; Wolfgang N Loescher; Martin Sawires; Michael Schocke; Klaus Seppi; Werner Poewe
Axial myopathy in parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2011;26(8):1569-71.
2010: Harald Hegen; Julia Wanschitz; Rainer Ehling; Florian Deisenhammer; Wolfgang N Löscher; Markus Reindl; Thomas Berger
Anti-alpha B-crystallin immunoreactivity in Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy.
Journal of the peripheral nervous system : JPNS 2010;15(2):150-2.
2009: Gabriel Miltenberger-Miltenyi; Thomas Schwarzbraun; Wolfgang N Löscher; Julia Wanschitz; Christian Windpassinger; Hans-Christoph Duba; Rainer Seidl; Gerhard Albrecht; Helga Weirich-Schwaiger; Heinz Zoller; Gerd Utermann; Michaela Auer-Grumbach; Andreas R Janecke
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.
European journal of human genetics : EJHG 2009;17(9):1154-9.
2008: Julia Wanschitz; Rainer Ehling; Wolfgang N Löscher; Betinna Künz; Florian Deisenhammer; Jens Kuhle; Herbert Budka; Markus Reindl; Thomas Berger
Intrathecal anti-alphaB-crystallin IgG antibody responses: potential inflammatory markers in Guillain-Barré syndrome.
Journal of neurology 2008;255(6):917-24.
2007: Margot Egger; Wilfried Schgoer; Arno G E Beer; Johannes Jeschke; Johannes Leierer; Markus Theurl; Silke Frauscher; Oren M Tepper; Andreas Niederwanger; Andreas Ritsch; Marianne Kearney; Julia Wanschitz; Geoffrey C Gurtner; Reiner Fischer-Colbrie; Günter Weiss; Hildegunde Piza-Katzer; Douglas Losordo; Josef R Patsch; Peter Schratzberger; Rudolf Kirchmair
Hypoxia up-regulates the angiogenic cytokine secretoneurin via an HIF-1alpha- and basic FGF-dependent pathway in muscle cells.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007;21(11):2906-17.
2007: Gabriel Miltenberger-Miltenyi; Andreas R Janecke; Julia Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N Löscher
Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.
Archives of neurology 2007;64(7):966-70.
2006: Julia Wanschitz; Wolfgang Dichtl; Herbert Budka; Wolfgang N Löscher; Sylvia Boesch
Acute motor and sensory axonal neuropathy in Burkitt-like lymphoma.
Muscle & nerve 2006;34(4):494-8.
2005: Petri Luoma; Ningguang Luo; Wolfgang N Löscher; Carol L Farr; Rita Horvath; Julia Wanschitz; Stefan Kiechl; Laurie S Kaguni; Anu Suomalainen
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.
Human molecular genetics 2005;14(14):1907-20.
2004: Rainer Ehling; Andreas Lutterotti; Julia Wanschitz; Michael Khalil; Claudia Gneiss; Florian Deisenhammer; Markus Reindl; Thomas Berger
Increased frequencies of serum antibodies to neurofilament light in patients with primary chronic progressive multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 2004;10(6):601-6.
2004: Wolfgang N Löscher; Julia Wanschitz; Karlheinz Reiners; Stefan Quasthoff
Morvan's syndrome: clinical, laboratory, and in vitro electrophysiological studies.
Muscle & nerve 2004;30(2):157-63.
2004: Stefan Kiechl; Rita Horváth; Petri Luoma; Ursula Kiechl-Kohlendorfer; B Wallacher-Scholz; Rolf Stucka; C Thaler; Julia Wanschitz; Anu Suomalainen; Michaela Jaksch; Johann Willeit
Two families with autosomal dominant progressive external ophthalmoplegia.
Journal of neurology, neurosurgery, and psychiatry 2004;75(8):1125-8.
2003: Julia Wanschitz; Hans Maier; Hans Lassmann; Herbert Budka; Thomas Berger
Distinct time pattern of complement activation and cytotoxic T cell response in Guillain-Barré syndrome.
Brain : a journal of neurology 2003;126(Pt 9):2034-42.
2001: Josef Finsterer; Claudia Stöllberger; Julia Wanschitz; Michaela Jaksch; Herbert Budka
Nail-patella syndrome associated with respiratory chain disorder.
European neurology 2001;46(2):92-5.