Vander Cruyssen, Bert, WESTHOVENS, R, DUREZ, P, VAN DEN BOSCH, FILIP, Mielants, Herman, DE CLERCK, L, ...
Vander Cruyssen, Bert, WESTHOVENS, R, DUREZ, P, Van Den Bosch, Filip, Mielants, Herman, DE CLERCK, L, ...
Vander Cruyssen, Bert, Van Looy, Stijn, Wyns, Bart, WESTHOVENS, R, DUREZ, P, Van Den Bosch, Filip, ...
Healthcare consumption and direct costs of rheumatoid arthritis in Belgium (2005)
Boonen, A, Verbruggen, L, Durez, P, De Clerck, L, Malaise, M, ...
The aim of this study was to compare the socioeconomic consequences of early and late rheumatoid arthritis in Belgium and to assess the patient out-of-pocket contributions. This multicentre...
Cruyssen, B, Van Looy, S, Wyns, B, Westhovens, R, Durez, P, Malaise, M, ...
This study is based on an expanded access program in which 511 patients suffering from active refractory rheumatoid arthritis (RA) were treated with intravenous infusions of infliximab (3 mg/kg+...
Vander Cruyssen, Bert, Van Looy, Stijn, WESTHOVENS, R, DUREZ, P, Van Den Bosch, Filip, VEYS, EM, ...
Healthcare consumption and direct costs of rheumatoid arthritis in Belgium (2005)
WESTHOVENS, R, BOONEN, A, VERBRUGGEN, L, DUREZ, P, DE CLERCK, L, MALAISE, M, ...
DAS28 is a robust measure of the physician's clinical judgment of response infliximab therapy (2005)
Vander Cruyssen, Bert, Van Looy, Stijn, Wyns, Bart, WESTHOVENS, R, DUREZ, P, ...
Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease (2004)
Van Hul, E, Van Driessche, K, Fransen, E, Devogelaer, J-P, Vanhoenacker, F, ...
A positional cloning effort in French Canadian families with Paget's disease of bone (PDB) resulted in the identification of a mutation in the sequestosome1 (SQSTM1) gene in a subset of both familial...
Chemical constituents and biological activities of Zanthoxylum usambarense. (2002)
He, Weidong, Van Puyvelde, Luc, De Kimpe, Norbert, VERBRUGGEN, L, ANTHONISSEN, K, ...
Evaluation of the role of RANK and OPG genes in Paget's disease of bone (2001)
Van Wesenbeeck, L, Morales-Piga, A, Ralston, S, Hocking, L, Vanhoenacker, F, ...
Paget's disease of bone (PDB) is one of the most common bone disorders in the western world. PDB is characterized by focal areas of increased osteoclastic bone resorption and bone formation, which...
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13
Janssens, K., Gershoni-Baruch, R., Van Hul, E., Brik, R., Guanabens, N., Migone, N., ...
Camurati-Engelmann disease, progressive diaphyseal dysplasia, or diaphyseal dysplasia Camurati-Engelmann is a rare, autosomal dominantly inherited bone disease, characterised by progressive cortical...
Janssens, K, Vanhoenacker, F, Bonduelle, M, Verbruggen, L, Van Maldergem, L, Ralston, S, ...
Camurati‐Engelmann disease (CED) is a rare autosomal dominant type of bone dysplasia. This review is based on the unpublished and detailed clinical, radiological, and molecular findings in 14 CED...
Chung, P. Y. J., Beyens, G., Riches, P. L., Van Wesenbeeck, L., Jennes, K., Daroszewska, A., ...
[Chung, P. Y. J.; Beyens, G.; Van Wesenbeeck, L.; Jennes, K.; Van Hul, W.] Univ Antwerp, Dept Med Genet, B-2020 Antwerp, Belgium. [Chung, P. Y. J.; Beyens, G.; Van Wesenbeeck, L.; Jennes, K.; Van...