Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (2) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (6) Blume, Alexander Dr. (1) Daniel, Peter Prof. Dr. (1) Daumke, Oliver Prof. Dr. (1) Dechend, Ralf Priv. Doz. (1) Diecke, Sebastian Dr. (3) Di Virgilio, Michela Prof. Dr. (2) Escobar Fernandez, Helena Dr. (14) Fielitz, Jens Dr. (6) Fischer, Cornelius Dr. (1) Franke, Vedran Dr. (1) Gouti, Mina Dr. (1) Henssen, Anton Prof. Dr. med. (1) Heuser, Arnd Dr. (1) Hübner, Norbert Prof. Dr. (4) Hummel, Oliver (1) Ignak, Busem (1) Izsvak, Zsuzsanna Dr. (2) Janke, Jürgen Dr. (1) Kabuss, Loreen-Claudine (1) Kempa, Stefan Dr. (3) Kieshauer, Janine (4) Kirchner, Marieluise Dr. (1) Kirwan, Jennifer Dr. (1) Koch, Katharina Sarah (1) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (2) Kunz, Severine Dr. (5) Lahmann, Ines Dr. (2) Lewin, Gary Prof. Dr. (1) Luft, Friedrich Prof. Dr. (4) Mahmoodzadeh, Shokoufeh PD Dr. (1) Marg, Andreas Dr. (16) Mertins, Philipp Dr. (1) Morano, Ingo Prof. Dr. (2) Müthel, Stefanie (6) Nazare, Marc (1) Perrot, Andreas (5) Popp, Oliver Dr. (1) Preibisch, Stephan Dr. (1) Qadri, Fatimunnisa Dr. (1) Rajewsky, Nikolaus Prof. Dr. (1) Saar, Kathrin Dr. (1) Schulz-Menger, Jeanette Prof. Dr. (6) Selbach, Matthias Prof. Dr. (1) Spuler, Simone Prof. (115) Stadelmann, Christian (2) Steinecker, Maria (1) Sunaga-Franze, Daniele Yumi Dr. (1) Telugu, Narasimha Swamy Dr. (2) Tursun, Baris Dr. (2) Wenzel, Katrin Dr. (6) Wolf, 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girdle muscular dystrophy R2 are the same disease U. Moore H. Gordish J. Diaz-Manera M.K. James A.G. Mayhew M. Guglieri R.F. Torron L.E. Rufibach J. Feng A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver E. Pegoraro L.P. Lowes J.R. Mendell K. Bushby V. Straub May 01, 2021 / Ann Neurol Assessing dysferlinopathy patients over three years with a new motor scale M. Jacobs M.K. James L.P. Lowes L.N. Alfano M. Eagle R.M. Lofra U. Moore J. Feng L.E. Rufibach K. Rose T. Duong L. Bello I. Pedrosa-Hernández S. Holsten C. Sakamoto A. Canal N.S.A. Práxedes S. Thiele C. Siener B. Vandevelde B. DeWolf E. Maron M. Guglieri J.Y. Hogrel A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver J. Díaz-Manera E. Pegoraro J.R. Mendell A.G. Mayhew V. Straub August 01, 2021 / Internist Diagnostik und Therapie von statinassoziierten Muskelsymptomen [Diagnostics and treatment of statin-associated muscle symptoms] U. Kassner S. Grunwald D. Spira N. Buchmann T. Bobbert E. Gazzerro T. Hollstein S. Spuler E. Steinhagen-Thiessen March 01, 2018 / Stem Cell Res Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene V. Meraviglia P. Benzoni S. Landi C. Murano M. Langione B.M. Motta S. Baratto R. Silipigni M. Di Segni P.P. Pramstaller D. DiFrancesco E. Gazzerro A. Barbuti A. Rossini December 18, 2019 / Nat Commun Human muscle-derived CLEC14A-positive cells regenerate muscle independent of PAX7 A. Marg H. Escobar Fernandez N. Karaiskos S.A. Grunwald E. Metzler J. Kieshauer S. Sauer D. Pasemann E. Malfatti D. Mompoint S. Quijano-Roy A. Boltengagen J. Schneider M. Schülke S. Kunz R. Carlier C. Birchmeier H. Amthor A. Spuler C. Kocks N. Rajewsky S. Spuler January 01, 2010 / Ann Neurol Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation H. Knoblauch C. Geier S. Adams B. Budde A. Rudolph U. Zacharias J. Schulz-Menger A. Spuler R.B. Yaou P. Nuernberg T. Voit G. Bonne S. Spuler February 09, 2010 / Circulation Cardiac involvement in sporadic inclusion-body myositis W. Utz S. Schmidt J. Schulz-Menger F. Luft S. Spuler March 12, 2010 / PLoS Genet Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations A. Rajab V. Straub L.J. McCann D. Seelow R. Varon R. Barresi A. Schulze B. Lucke S. Luetzkendorf M. Karbasiyan S. Bachmann S. Spuler M. Schuelke April 15, 2010 / Mov Disord Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach S. Spuler H. Krug C. Klein I.C. Medialdea W. Jakob G. Ebersbach D. Gruber K.T. Hoffmann T. Trottenberg A. Kupsch June 15, 2015 / Am J Physiol Cell Physiol Cavin 1 function does not follow caveolar morphology T. Timmel S. Kunz F. Seifert M. Schuelke S. Spuler Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
April 01, 2021 / Neuromuscul Disord Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same disease U. Moore H. Gordish J. Diaz-Manera M.K. James A.G. Mayhew M. Guglieri R.F. Torron L.E. Rufibach J. Feng A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver E. Pegoraro L.P. Lowes J.R. Mendell K. Bushby V. Straub
May 01, 2021 / Ann Neurol Assessing dysferlinopathy patients over three years with a new motor scale M. Jacobs M.K. James L.P. Lowes L.N. Alfano M. Eagle R.M. Lofra U. Moore J. Feng L.E. Rufibach K. Rose T. Duong L. Bello I. Pedrosa-Hernández S. Holsten C. Sakamoto A. Canal N.S.A. Práxedes S. Thiele C. Siener B. Vandevelde B. DeWolf E. Maron M. Guglieri J.Y. Hogrel A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver J. Díaz-Manera E. Pegoraro J.R. Mendell A.G. Mayhew V. Straub
August 01, 2021 / Internist Diagnostik und Therapie von statinassoziierten Muskelsymptomen [Diagnostics and treatment of statin-associated muscle symptoms] U. Kassner S. Grunwald D. Spira N. Buchmann T. Bobbert E. Gazzerro T. Hollstein S. Spuler E. Steinhagen-Thiessen
March 01, 2018 / Stem Cell Res Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene V. Meraviglia P. Benzoni S. Landi C. Murano M. Langione B.M. Motta S. Baratto R. Silipigni M. Di Segni P.P. Pramstaller D. DiFrancesco E. Gazzerro A. Barbuti A. Rossini
December 18, 2019 / Nat Commun Human muscle-derived CLEC14A-positive cells regenerate muscle independent of PAX7 A. Marg H. Escobar Fernandez N. Karaiskos S.A. Grunwald E. Metzler J. Kieshauer S. Sauer D. Pasemann E. Malfatti D. Mompoint S. Quijano-Roy A. Boltengagen J. Schneider M. Schülke S. Kunz R. Carlier C. Birchmeier H. Amthor A. Spuler C. Kocks N. Rajewsky S. Spuler
January 01, 2010 / Ann Neurol Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation H. Knoblauch C. Geier S. Adams B. Budde A. Rudolph U. Zacharias J. Schulz-Menger A. Spuler R.B. Yaou P. Nuernberg T. Voit G. Bonne S. Spuler
February 09, 2010 / Circulation Cardiac involvement in sporadic inclusion-body myositis W. Utz S. Schmidt J. Schulz-Menger F. Luft S. Spuler
March 12, 2010 / PLoS Genet Fatal cardiac arrhythmia and long-QT syndrome in a new form of congenital generalized lipodystrophy with muscle rippling (CGL4) due to PTRF-CAVIN mutations A. Rajab V. Straub L.J. McCann D. Seelow R. Varon R. Barresi A. Schulze B. Lucke S. Luetzkendorf M. Karbasiyan S. Bachmann S. Spuler M. Schuelke
April 15, 2010 / Mov Disord Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach S. Spuler H. Krug C. Klein I.C. Medialdea W. Jakob G. Ebersbach D. Gruber K.T. Hoffmann T. Trottenberg A. Kupsch
June 15, 2015 / Am J Physiol Cell Physiol Cavin 1 function does not follow caveolar morphology T. Timmel S. Kunz F. Seifert M. Schuelke S. Spuler