Orphan Peripheral Neuropathies

por Finsterer, Josef, Löscher, Wolfgang N., Wanschitz, Julia, Iglseder, Stefan
Publicado 2021

Are neurological complications of monoclonal gammopathy of undetermined significance underestimated?

por Steiner, Normann, Schwärzler, Angelika, Göbel, Georg, Löscher, Wolfgang, Wanschitz, Julia, Gunsilius, Eberhard
Publicado 2016

New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant: Time for Acute Genetic Testing Before Treatment?

por Indelicato, Elisabetta, Pfeilstetter, Johannes, Zech, Michael, Unterberger, Iris, Wanschitz, Julia, Berweck, Steffen, Boesch, Sylvia
Publicado 2023

Bioenergetics of the Calf Muscle in Friedreich Ataxia Patients Measured by 31P-MRS Before and After Treatment with Recombinant Human Erythropoietin

por Nachbauer, Wolfgang, Boesch, Sylvia, Schneider, Rainer, Eigentler, Andreas, Wanschitz, Julia, Poewe, Werner, Schocke, Michael
Publicado 2013

Transcranial Magnetic Stimulation in the Differential Diagnosis of Unilateral Peripheral Facial Nerve Palsy

por Kleinveld, Vera E. A., Platzgummer, Sarah, Wanschitz, Julia, Horlings, Corinne G. C., Löscher, Wolfgang N.
Publicado 2023

Skeletal muscle proteome analysis underpins multifaceted mitochondrial dysfunction in Friedreich’s ataxia

por Indelicato, Elisabetta, Faserl, Klaus, Amprosi, Matthias, Nachbauer, Wolfgang, Schneider, Rainer, Wanschitz, Julia, Sarg, Bettina, Boesch, Sylvia
Publicado 2023

Amyloid myopathy: expanding the clinical spectrum of transthyretin amyloidosis—case report and literature review

por Ungericht, Maria, Wanschitz, Julia, Kroiss, Alexander S., Röcken, Christoph, Schuetz, Thomas, Messner, Moritz, Zaruba, Marc-Michael, Loescher, Wolfgang N., Poelzl, Gerhard
Publicado 2022

Cerebrospinal fluid protein in Guillain–Barré syndrome: Need for age‐dependent interpretation

por Hegen, Harald, Ladstätter, Felix, Bsteh, Gabriel, Auer, Michael, Berek, Klaus, Di Pauli, Franziska, Walde, Janette, Wanschitz, Julia, Zinganell, Anne, Deisenhammer, Florian
Publicado 2020

Autonomic function testing in Friedreich’s ataxia

por Indelicato, Elisabetta, Fanciulli, Alessandra, Ndayisaba, Jean-Pierre, Nachbauer, Wolfgang, Eigentler, Andreas, Granata, Roberta, Wanschitz, Julia, Poewe, Werner, Wenning, Gregor K., Boesch, Sylvia
Publicado 2018

Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the Phenotype

por Kuzdas-Wood, Daniela, Irschick, Regina, Theurl, Markus, Malsch, Philipp, Mair, Norbert, Mantinger, Christine, Wanschitz, Julia, Klimaschewski, Lars, Poewe, Werner, Stefanova, Nadia, Wenning, Gregor K.
Publicado 2015

Autonomic function testing in spinocerebellar ataxia type 2

por Indelicato, Elisabetta, Fanciulli, Alessandra, Ndayisaba, Jean Pierre, Nachbauer, Wolfgang, Granata, Roberta, Wanschitz, Julia, Wagner, Michaela, Gizewski, Elke R., Poewe, Werner, Wenning, Gregor K., Boesch, Sylvia
Publicado 2018

Skeletal muscle transcriptomics dissects the pathogenesis of Friedreich’s ataxia

por Indelicato, Elisabetta, Kirchmair, Alexander, Amprosi, Matthias, Steixner, Stephan, Nachbauer, Wolfgang, Eigentler, Andreas, Wahl, Nico, Apostolova, Galina, Krogsdam, Anne, Schneider, Rainer, Wanschitz, Julia, Trajanoski, Zlatko, Boesch, Sylvia
Publicado 2023

Bisphosphonates in multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder – an alternative therapeutic approach

por Pichler, Karin, Karall, Daniela, Kotzot, Dieter, Steichen-Gersdorf, Elisabeth, Rümmele-Waibel, Alexandra, Mittaz-Crettol, Laureane, Wanschitz, Julia, Bonafé, Luisa, Maurer, Kathrin, Superti-Furga, Andrea, Scholl-Bürgi, Sabine
Publicado 2016

Myasthenic crisis following SARS-CoV-2 infection and delayed virus clearance in a patient treated with rituximab: clinical course and 6-month follow-up

por Wanschitz, Julia V., Kaml, Manuela, Pfausler, Bettina, Helbok, Raimund, Wildner, Sophie, Widmann, Gerlig, Sahanic, Sabina, Deisenhammer, Florian, Löscher, Wolfgang N., Reindl, Markus, Löffler-Ragg, Judith, Beer, Ronny
Publicado 2020

Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis

por Wanschitz, Julia V., Dubourg, Odile, Lacene, Emmanuelle, Fischer, Michael B., Höftberger, Romana, Budka, Herbert, Romero, Norma B., Eymard, Bruno, Herson, Serge, Butler-Browne, Gillian S., Voit, Thomas, Benveniste, Olivier
Publicado 2013

Th1 Response and Systemic Treg Deficiency in Inclusion Body Myositis

por Allenbach, Yves, Chaara, Wahiba, Rosenzwajg, Michelle, Six, Adrien, Prevel, Nicolas, Mingozzi, Federico, Wanschitz, Julia, Musset, Lucile, Charuel, Jean-Luc, Eymard, Bruno, Salomon, Benoit, Duyckaerts, Charles, Maisonobe, Thierry, Dubourg, Odile, Herson, Serge, Klatzmann, David, Benveniste, Olivier
Publicado 2014

Muscle involvement in SARS‐CoV‐2 infection

por Pitscheider, Lea, Karolyi, Mario, Burkert, Francesco R., Helbok, Raimund, Wanschitz, Julia V., Horlings, Corinne, Pawelka, Erich, Omid, Sara, Traugott, Marianna, Seitz, Tamara, Zoufaly, Alexander, Lindeck‐Pozza, Elisabeth, Wöll, Ewald, Beer, Ronny, Seiwald, Stefanie, Bellmann‐Weiler, Rosa, Hegen, Harald, Löscher, Wolfgang N.
Publicado 2020

Small fiber involvement is independent from clinical pain in late-onset Pompe disease

por Enax-Krumova, Elena K., Dahlhaus, Iris, Görlach, Jonas, Claeys, Kristl G., Montagnese, Federica, Schneider, llka, Sturm, Dietrich, Fangerau, Tanja, Schlierbach, Hannah, Roth, Angela, Wanschitz, Julia V., Löscher, Wolfgang N., Güttsches, Anne-Katrin, Vielhaber, Stefan, Hasseli, Rebecca, Zunk, Lea, Krämer, Heidrun H., Hahn, Andreas, Schoser, Benedikt, Rosenbohm, Angela, Schänzer, Anne
Publicado 2022

Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathy

por De Simoni, Desiree, Ricken, Gerda, Winklehner, Michael, Koneczny, Inga, Karenfort, Michael, Hustedt, Ulf, Seidel, Ulrich, Abdel-Mannan, Omar, Munot, Pinki, Rinaldi, Simon, Steen, Claudia, Freilinger, Michael, Breu, Markus, Seidl, Rainer, Reindl, Markus, Wanschitz, Julia, Lleixà, Cinta, Bernert, Günther, Wandinger, Klaus-Peter, Junker, Ralf, Querol, Luis, Leypoldt, Frank, Rostásy, Kevin, Höftberger, Romana
Publicado 2020

Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study

por 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, Hohenwarter, Christina, Freimüller, Manfred, Embacher, Norbert, Wanschitz, Julia, Topakian, Raffi, Töpf, Ana, Straub, Volker, Quasthoff, Stefan, Zimprich, Fritz, Löscher, Wolfgang N., Cetin, Hakan
Publicado 2022