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Infections and vaccinations preceding childhood Guillain-Barré syndrome: a prospective study.
Published in:
2006
By:
- Schessl, Joachim;
- Luther, Birgit;
- Kirschner, Janbernd;
- Mauff, Gottfried;
- Korinthenberg, Rudolf
Publication type:
journal article
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
Published in:
Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-26
By:
- Walter, Maggie C.;
- Reilich, Peter;
- Thiele, Simone;
- Schessl, Joachim;
- Schreiber, Herbert;
- Reiners, Karlheinz;
- Kress, Wolfram;
- Müller-Reible, Clemens;
- Vorgerd, Matthias;
- Urban, Peter;
- Schrank, Bertold;
- Deschauer, Marcus;
- Schlotter-Weigel, Beate;
- Kohnen, Ralf;
- Lochmüller, Hanns
Publication type:
Article
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
Published in:
2013
By:
- Walter, Maggie C;
- Reilich, Peter;
- Thiele, Simone;
- Schessl, Joachim;
- Schreiber, Herbert;
- Reiners, Karlheinz;
- Kress, Wolfram;
- Müller-Reible, Clemens;
- Vorgerd, Matthias;
- Urban, Peter;
- Schrank, Bertold;
- Deschauer, Marcus;
- Schlotter-Weigel, Beate;
- Kohnen, Ralf;
- Lochmüller, Hanns
Publication type:
journal article
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy.
Published in:
2008
By:
- Schessl, Joachim;
- Yaqun Zou;
- McGrath, Meagan J.;
- Cowling, Belinda S.;
- Maiti, Baijayanta;
- Chin, Steven S.;
- Sewry, Caroline;
- Battini, Roberta;
- Ying Hu;
- Cottle, Denny L.;
- Rosenblatt, Michael;
- Spruce, Lynn;
- Ganguly, Arupa;
- Kirschner, Janbernd;
- Judkins, Alexander R.;
- Golden, Jeffrey A.;
- Goebel, Hans-Hilmar;
- Muntoni, Francesco;
- Flanigan, Kevin M.;
- Mitchell, Christina A.
Publication type:
journal article
Severe Obstructive Sleep Apnea Alleviated by Oral Appliance in a Three-Year-Old Boy.
Published in:
Respiration, 2008, v. 76, n. 1, p. 112, doi. 10.1159/000098407
By:
- Schessl, Joachim;
- Rose, Edmund;
- Korinthenberg, Rudolf;
- Henschen, Matthias
Publication type:
Article
Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and miyoshi type of muscular dystrophy.
Published in:
Muscle & Nerve, 2012, v. 45, n. 5, p. 740, doi. 10.1002/mus.23281
By:
- Schessl, Joachim;
- Kress, Wolfram;
- Schoser, Benedikt
Publication type:
Article
Predominant fiber atrophy and fiber type disproportion in early ullrich disease.
Published in:
Muscle & Nerve, 2008, v. 38, n. 3, p. 1184, doi. 10.1002/mus.21088
By:
- Schessl, Joachim;
- Goemans, Nathalie M.;
- Magold, Alexandra I.;
- Zou, Yaqun;
- Hu, Ying;
- Kirschner, Janbernd;
- Sciot, Raf;
- Bönnemann, Carsten G.
Publication type:
Article
Patient-specific protein aggregates in myofibrillar myopathies: Laser microdissection and differential proteomics for identification of plaque components.
Published in:
Proteomics, 2012, v. 12, n. 23/24, p. 3598, doi. 10.1002/pmic.201100559
By:
- Feldkirchner, Sarah;
- Schessl, Joachim;
- Müller, Stefan;
- Schoser, Benedikt;
- Hanisch, Franz-Georg
Publication type:
Article
Role of GluR1 in Activity-Dependent Motor System Development.
Published in:
Journal of Neuroscience, 2008, v. 28, n. 40, p. 9953, doi. 10.1523/JNEUROSCI.0880-08.2008
By:
- Lei Zhang;
- Schessl, Joachim;
- Werner, Markus;
- Bonnemann, Carsten;
- Guoxiang Xiong;
- Mojsilovic-Petrovic, Jelena;
- Weiguo Zhou;
- Cohen, Akiva;
- Seeburg, Peter;
- Misawa, Hidemi;
- Jayaram, Aditi;
- Personius, Kirkwood;
- Hollmann, Michael;
- Sprengel, Rolf;
- Kalb, Robert
Publication type:
Article
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family.
Published in:
JAMA Neurology, 2015, v. 72, n. 6, p. 689, doi. 10.1001/jamaneurol.2015.37
By:
- Zukosky, Kristen;
- Meilleur, Katherine;
- Traynor, Bryan J.;
- Dastgir, Jahannaz;
- Medne, Livija;
- Devoto, Marcella;
- Collins, James;
- Rooney, Jachinta;
- Yaqun Zou;
- Yang, Michele L.;
- Gibbs, J. Raphael;
- Meier, Markus;
- Stetefeld, Joerg;
- Finkel, Richard S.;
- Schessl, Joachim;
- Elman, Lauren;
- Felice, Kevin;
- Ferguson, Toby A.;
- Ceyhan-Birsoy, Ozge;
- Beggs, Alan H.
Publication type:
Article
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
Published in:
Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 452, doi. 10.1093/brain/awn325
By:
- Joachim Schessl;
- Ana L. Taratuto;
- Caroline Sewry;
- Roberta Battini;
- Steven S. Chin;
- Baijayanta Maiti;
- Alberto L. Dubrovsky;
- Marcela G. Erro;
- Graciela Espada;
- Monica Robertella;
- Maria Saccoliti;
- Patricia Olmos;
- Leslie R. Bridges;
- Peter Standring;
- Ying Hu;
- Yaqun Zou;
- Kathryn J. Swoboda;
- Mena Scavina;
- Hans-Hilmar Goebel;
- Christina A. Mitchell
Publication type:
Article
Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy.
Published in:
Journal of Cell Biology, 2008, v. 183, n. 6, p. 1033, doi. 10.1083/jcb.200804077
By:
- Cowling, Belinda S.;
- McGrath, Meagan J.;
- Nguyen, Mai-Anh;
- Cottle, Denny L.;
- Kee, Anthony J.;
- Brown, Susan;
- Schessl, Joachim;
- Yaqun Zou;
- Joya, Josephine;
- Bönnemann, Carsten G.;
- Hardeman, Edna C.;
- Mitchel, Christina A.
Publication type:
Article
Impact of the coronavirus disease 2019 pandemic on stroke teleconsultations in Germany in the first half of 2020.
Published in:
European Journal of Neurology, 2021, v. 28, n. 10, p. 3267, doi. 10.1111/ene.14787
By:
- Vollmuth, Christoph;
- Miljukov, Olga;
- Abu‐Mugheisib, Mazen;
- Angermaier, Anselm;
- Barlinn, Jessica;
- Busetto, Loraine;
- Grau, Armin J.;
- Guenther, Albrecht;
- Gumbinger, Christoph;
- Hubert, Nikolai;
- Hüttemann, Katrin;
- Klingner, Carsten;
- Naumann, Markus;
- Palm, Frederick;
- Remi, Jan;
- Rücker, Viktoria;
- Schessl, Joachim;
- Schlachetzki, Felix;
- Schuppner, Ramona;
- Schwab, Stefan
Publication type:
Article
Safety and tolerability of intravenous immunoglobulin in patients with active dermatomyositis: results from the randomised, placebo-controlled ProDERM study.
Published in:
Arthritis Research & Therapy, 2024, v. 26, n. 1, p. 1, doi. 10.1186/s13075-023-03232-2
By:
- Aggarwal, Rohit;
- Schessl, Joachim;
- Charles-Schoeman, Christina;
- Bata-Csörgő, Zsuzsanna;
- Dimachkie, Mazen M.;
- Griger, Zoltan;
- Moiseev, Sergey;
- Oddis, Chester V.;
- Schiopu, Elena;
- Vencovský, Jiri;
- Beckmann, Irene;
- Clodi, Elisabeth;
- Levine, Todd
Publication type:
Article
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
Published in:
Neurogenetics, 2014, v. 15, n. 3, p. 151, doi. 10.1007/s10048-014-0410-4
By:
- Schessl, Joachim;
- Bach, Elisa;
- Rost, Simone;
- Feldkirchner, Sarah;
- Kubny, Christiana;
- Müller, Stefan;
- Hanisch, Franz-Georg;
- Kress, Wolfram;
- Schoser, Benedikt
Publication type:
Article

Found: 15