L
Leon Verbruggen
Researcher at Vrije Universiteit Brussel
Publications - 52
Citations - 2409
Leon Verbruggen is an academic researcher from Vrije Universiteit Brussel. The author has contributed to research in topics: Arthritis & Rheumatoid arthritis. The author has an hindex of 19, co-authored 52 publications receiving 2344 citations. Previous affiliations of Leon Verbruggen include National Institutes of Health.
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Journal ArticleDOI
Intravenous zoledronic acid in postmenopausal women with low bone mineral density.
Ian R. Reid,Jacques P. Brown,Peter Burckhardt,Zebulun D. Horowitz,P J Richardson,Ulrich Trechsel,A Widmer,Jean-Pierre Devogelaer,Jean-Marc Kaufman,Philippe Jaeger,Jean-Jacques Body,Maria Luisa Brandi,Johann Broell,Raffaele Di Micco,Andrea R. Genazzani,Dieter Felsenberg,Joachim Happ,Michael J. Hooper,Jochen Ittner,Georg Leb,Hans Mallmin,Timothy M. Murray,Sergio Ortolani,Alessandro Rubinacci,Maria Sääf,Göran Samsioe,Leon Verbruggen,Pierre J. Meunier +27 more
TL;DR: Zoledronic acid infusions given at intervals of up to one year produce effects on bone turnover and bone density as great as those achieved with daily oral dosing with bisphosphonates with proven efficacy against fractures, suggesting that an annual infusion of zoledronic Acid might be an effective treatment for postmenopausal osteoporosis.
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Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment
Katrien Janssens,Filip Vanhoenacker,Mary-Louise Bonduelle,Leon Verbruggen,L. Van Maldergem,Stuart H. Ralston,Núria Guañabens,N. Migone,S Wientroub,Maria Teresa Divizia,Carsten Bergmann,Christopher P. Bennett,S Simsek,S Melançon,Tim Cundy,W. Van Hul +15 more
TL;DR: The detailed description of such a large set of CED patients will be of value in establishing the correct diagnosis, genetic counselling, and treatment, and the overview of possible treatments, diagnostic guidelines, and considerations for prenatal testing is provided.
Journal ArticleDOI
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease.
Katrien Janssens,R. Gershoni-Baruch,Núria Guañabens,N. Migone,Stuart H. Ralston,Mary-Louise Bonduelle,Willy Lissens,L. Van Maldergem,Filip Vanhoenacker,Leon Verbruggen,W. Van Hul +10 more
TL;DR: TGFB1 was evaluated as a candidate gene for causing CED because this region contains the gene encoding transforming growth factor-β1, an important mediator of bone remodelling.
Journal ArticleDOI
Evaluation of the role of RANK and OPG genes in Paget’s disease of bone
Wim Wuyts,L. Van Wesenbeeck,A Morales-Piga,Stuart H. Ralston,Lynne J. Hocking,Filip Vanhoenacker,Rene Westhovens,Leon Verbruggen,D. M. Anderson,Anne E. Hughes,W. Van Hul +10 more
TL;DR: The data suggest that RANK is not directly involved in PDB in a set of patients, as no mutations in the RANK coding region could be identified and allele frequencies of RANK polymorphisms did not differ in P DB patients as compared with the random population.
Journal ArticleDOI
DAS28 best reflects the physician's clinical judgment of response to infliximab therapy in rheumatoid arthritis patients: validation of the DAS28 score in patients under infliximab treatment
Bert Vander Cruyssen,Stijn Van Looy,Bart Wyns,Rene Westhovens,Patrick Durez,Filip Van den Bosch,Eric Veys,Herman Mielants,Luc De Clerck,A. Peretz,Michel Malaise,Leon Verbruggen,Nathan Vastesaeger,A. Geldhof,Luc Boullart,Filip De Keyser +15 more
TL;DR: It is proved that the momentary DAS28 score correlates best with the treating rheumatologist's decision to increase the dose of infliximab (+MTX), which indicates an insufficient response to inflIXimab at 3 mg/kg in patients with RA.