K
Klaus W. Frommer
Researcher at University of Giessen
Publications - 55
Citations - 1295
Klaus W. Frommer is an academic researcher from University of Giessen. The author has contributed to research in topics: Adipokine & Bone remodeling. The author has an hindex of 15, co-authored 53 publications receiving 1057 citations.
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Journal ArticleDOI
Update on the profile of the EUSTAR cohort: an analysis of the EULAR Scleroderma Trials and Research group database
Florian M P Meier,Klaus W. Frommer,Robert Dinser,Ulrich A Walker,László Czirják,Christopher P. Denton,Yannick Allanore,Oliver Distler,Gabriela Riemekasten,Gabriele Valentini,Ulf Müller-Ladner +10 more
TL;DR: A database to prospectively gather key data of patients with SSc using a minimal essential dataset provides an abundance of information on the true clinical face of SSc that will be helpful in improving the classification of S Sc and its subsets and for developing more specific therapeutic recommendations.
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Adiponectin-mediated changes in effector cells involved in the pathophysiology of rheumatoid arthritis.
Klaus W. Frommer,Birgit Zimmermann,Florian M P Meier,D Schröder,Matthias Heil,Andreas Schäffler,Christa Büchler,Jürgen Steinmeyer,Fabia Brentano,Ulf Müller-Ladner,Elena Neumann +10 more
TL;DR: The findings of the present study indicate that adiponectin induces gene expression and protein synthesis in human RASFs, lymphocytes, endothelial cells, and chondrocytes, supporting the concept of adip onectin being involved in the pathophysiologic modulation of RA effector cells.
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Adipocytokines as driving forces in rheumatoid arthritis and related inflammatory diseases
TL;DR: The current knowledge about the influence of central adipokines in rheumatic diseases, highlighting several aspects of the role of adipokine in chronic inflammation, is summarized.
Journal ArticleDOI
Adipokines in bone disease.
TL;DR: Current knowledge relating to adipokines in rheumatic diseases is summarized, with a particular focus on the effects of adipokine on bone remodelling.
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Free fatty acids: potential proinflammatory mediators in rheumatic diseases
TL;DR: The data show that FFA are not only metabolic substrates but may also directly contribute to articular inflammation and degradation in inflammatory joint diseases and require extracellular and intracellular access to the TLR4 receptor complex.