Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Birchmeier, Walter Prof. Dr. (4) Birchmeier-Kohler, Carmen Prof. Dr. (24) Dechend, Ralf Priv. Doz. (1) Escobar Fernandez, Helena Dr. (1) Fielitz, Jens Dr. (2) Griffel, Carola (2) Grossmann, Katja Dr. (1) Izsvak, Zsuzsanna Dr. (1) Lewin, Gary Prof. Dr. (2) Marg, Andreas Dr. (1) Müller, Thomas Dr. (7) Qadri, Fatimunnisa Dr. (1) Rajewsky, Klaus Prof. Dr. (1) Rybak-Wolf, Agnieszka Dr. (1) Selbach, Matthias Prof. Dr. (2) Spagnoli, Francesca Dr. (1) Treier, Mathias Prof. Dr. (2) Wenzel, Katrin Dr. (1) (-) Hübner, Norbert Prof. Dr. (3) (-) Saar, Kathrin Dr. (1) (-) Spuler, Simone Prof. (15) 1992 (1) 1993 (2) 1994 (2) 1995 (1) 1996 (4) 1997 (3) 1998 (2) 1999 (2) 2002 (1) 2004 (1) 2005 (4) 2006 (3) (-) 2007 (4) 2008 (3) (-) 2009 (5) 2010 (9) 2011 (5) 2012 (5) 2013 (3) (-) 2014 (7) 2015 (2) 2016 (6) 2017 (3) 2018 (5) 2019 (6) 2020 (8) 2021 (6) 2022 (12) 2023 (5) 2024 (1) AG Müller/Dechend (ECRC) (1) Biology of Malignant Lymphomas (1) (-) Developmental Biology / Signal Transduction (2) Developmental Neurobiology (6) Endocrinology, Diabetes and Nutritional Medicine (3) Genetics and Genomics of Cardiovascular Diseases (40) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Microenvironmental Regulation in Autoimmunity and Cancer (1) Mobile DNA (3) Molecular Biology of Peptide Hormones (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (4) Molecular Physiology of Somatic Sensation (1) (-) Myology (15) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (4) Proteome Dynamics (2) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) RNA Biology and Posttranscriptional Regulation (2) Systems Biology of Gene Regulatory Elements (1) Translational Cardiology and Functional Genomics (2) Translational Oncology of Solid Tumors (1) 16 Results: Active Filter: Hübner, Norbert Prof. Dr.Saar, Kathrin Dr.Spuler, Simone Prof.Developmental Biology / Signal TransductionMyology200720092014 Sort: Result score Newest to oldest Oldest to newest May 01, 2009 / Pathologe Amyloidose bei Muskeldystrophie [Amyloidosis in muscular dystrophy] M. Carl C. Roecken S. Spuler September 01, 2009 / Am J Hum Genet Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy L. Gueneau A.T. Bertrand J.P. Jais M.A. Salih T. Stojkovic M. Wehnert M. Hoeltzenbein S. Spuler S. Saitoh A. Verschueren C. Tranchant M. Beuvin E. Lacene N.B. Romero S. Heath D. Zelenika T. Voit B. Eymard R. Ben Yaou G. Bonne July 01, 2009 / Diabetes Free fatty acids link metabolism and regulation of the insulin-sensitizing fibroblast growth factor-21 K. Mai J. Andres K. Biedasek J. Weicht T. Bobbert M. Sabath S. Meinus F. Reinecke M. Moehlig M.O. Weickert M. Clemenz A.F. Pfeiffer U. Kintscher S. Spuler J. Spranger September 01, 2009 / Crit Care Med Nonexcitable muscle membrane predicts intensive care unit-acquired paresis in mechanically ventilated, sedated patients S. Weber-Carstens S. Koch S. Spuler C.D. Spies F. Bubser K.D. Wernecke M. Deja January 01, 2009 / Radiology Dysferlin-deficient muscular dystrophy: Gadofluorine M suitability at MR imaging in a mouse model S. Schmidt A. Vieweger M. Obst S. Mueller V. Gross M. Gutberlet J. Steinbrink S. Taubert B. Misselwitz L. Luedemann S. Spuler November 01, 2007 / J Mol Med Dysfunction of dysferlin-deficient hearts K. Wenzel C. Geier F. Qadri N. Huebner H. Schulz B. Erdmann V. Gross D. Bauer R. Dechend R. Dietz K.J. Osterziel S. Spuler C. Oezcelik June 01, 2007 / J Clin Endocrinol Metab Peroxisome proliferator-activated receptor-gamma C190S mutation causes partial lipodystrophy A. Luedtke J. Buettner W. Wu A. Muchir A. Schroeter S. Zinn-Justin S. Spuler H.H. Schmidt H.J. Worman February 27, 2007 / Neurology Muscle and nerve pathology in Dunnigan familial partial lipodystrophy S. Spuler T. Kalbhenn J. Zabojszcza F.K. van Landeghem A. Ludtke K. Wenzel M. Koehnlein M. Schuelke L. Luedemann H.H. Schmidt February 01, 2007 / Neuromuscul Disord Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF A. Diers M. Carl G. Stoltenburg-Didinger M. Vorgerd S. Spuler September 01, 2014 / Muscle Nerve Long term recovery in critical illness myopathy is complete, contrary to polyneuropathy S. Koch T. Wollersheim J. Bierbrauer K. Haas R. Mörgeli M. Deja C.D. Spies S. Spuler M. Krebs S. Weber-Carstens Pagination Current page 1 Page 2 Next page Next › Last page Last »
May 01, 2009 / Pathologe Amyloidose bei Muskeldystrophie [Amyloidosis in muscular dystrophy] M. Carl C. Roecken S. Spuler
September 01, 2009 / Am J Hum Genet Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy L. Gueneau A.T. Bertrand J.P. Jais M.A. Salih T. Stojkovic M. Wehnert M. Hoeltzenbein S. Spuler S. Saitoh A. Verschueren C. Tranchant M. Beuvin E. Lacene N.B. Romero S. Heath D. Zelenika T. Voit B. Eymard R. Ben Yaou G. Bonne
July 01, 2009 / Diabetes Free fatty acids link metabolism and regulation of the insulin-sensitizing fibroblast growth factor-21 K. Mai J. Andres K. Biedasek J. Weicht T. Bobbert M. Sabath S. Meinus F. Reinecke M. Moehlig M.O. Weickert M. Clemenz A.F. Pfeiffer U. Kintscher S. Spuler J. Spranger
September 01, 2009 / Crit Care Med Nonexcitable muscle membrane predicts intensive care unit-acquired paresis in mechanically ventilated, sedated patients S. Weber-Carstens S. Koch S. Spuler C.D. Spies F. Bubser K.D. Wernecke M. Deja
January 01, 2009 / Radiology Dysferlin-deficient muscular dystrophy: Gadofluorine M suitability at MR imaging in a mouse model S. Schmidt A. Vieweger M. Obst S. Mueller V. Gross M. Gutberlet J. Steinbrink S. Taubert B. Misselwitz L. Luedemann S. Spuler
November 01, 2007 / J Mol Med Dysfunction of dysferlin-deficient hearts K. Wenzel C. Geier F. Qadri N. Huebner H. Schulz B. Erdmann V. Gross D. Bauer R. Dechend R. Dietz K.J. Osterziel S. Spuler C. Oezcelik
June 01, 2007 / J Clin Endocrinol Metab Peroxisome proliferator-activated receptor-gamma C190S mutation causes partial lipodystrophy A. Luedtke J. Buettner W. Wu A. Muchir A. Schroeter S. Zinn-Justin S. Spuler H.H. Schmidt H.J. Worman
February 27, 2007 / Neurology Muscle and nerve pathology in Dunnigan familial partial lipodystrophy S. Spuler T. Kalbhenn J. Zabojszcza F.K. van Landeghem A. Ludtke K. Wenzel M. Koehnlein M. Schuelke L. Luedemann H.H. Schmidt
February 01, 2007 / Neuromuscul Disord Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF A. Diers M. Carl G. Stoltenburg-Didinger M. Vorgerd S. Spuler
September 01, 2014 / Muscle Nerve Long term recovery in critical illness myopathy is complete, contrary to polyneuropathy S. Koch T. Wollersheim J. Bierbrauer K. Haas R. Mörgeli M. Deja C.D. Spies S. Spuler M. Krebs S. Weber-Carstens