Zobrazeno 1 - 10
of 138
pro vyhledávání: '"F, Rickaert"'
Publikováno v:
Mycoses. 30:449-453
One of the 1st known cases of disseminated histoplasmosis as a result of histoplasma duboisii was in a patient with AIDS. This patient a 38 year old caucasian was diagnosed in 1986 and had lived in Zaire from 1972 until 1978. There have been about 20
Autor:
Jacques Devière, Jean-Luc Van Laethem, F. Rickaert, Hubert Louis, Patrick Robberecht, Rally Eskinazi
Publikováno v:
Gut. 43:408-413
Background—Interleukin 10 (IL-10) decreases the severity of experimental acute pancreatitis. The role of endogenous IL-10 in modulating the course of pancreatitis is currently unknown.Aims—To examine the systemic release of IL-10 and its messenge
Autor:
J Van Rampelbergh, Michel Cremer, Pascale Vertongen, F. Rickaert, J.-L. Van Laethem, J. Devière, Patrick Robberecht
Publikováno v:
Gut. 36:781-787
Differential diagnosis of pancreatic cancer and chronic pancreatitis is sometimes difficult and cytological examination of brushings or aspirated material collected during endoscopic retrograde cholangiopancreatography (ERCP) remains disappointing. A
Publikováno v:
Revue medicale de Bruxelles. 31(6)
Intramural pseudodiverticulosis of the esophagus is a rare benign disease of the eosphageal wall, with dilation of the submucosal glands, and the predominant symptom is dysphagia. This disorder may be associated with gastroesophageal reflux, motility
Autor:
Carine Deprez, Frédérique Jacobs, Nadine Bourgeois, Françoise Moonens, Michel Gelin, Jean Van De Stadt, Michael Adler, Corinne Liesnard, Maria Lourdes Tavares, F. Rickaert
Publikováno v:
Journal of Hepatology. 18:284-289
Listeria is an uncommon cause of hepatitis in adults. We report the case of a liver transplant recipient who presented with a clinical picture of acute hepatitis, 8 months after grafting. Blood cultures yielded Listeria monocytogenes. The patient mad
Publikováno v:
Revue medicale de Bruxelles. 28(6)
We report the case of an autoimmune hepatitis in a 59-year old woman who was referred for a progressive jaundice. The patient had an history of CREST syndrome. The particularity of this case report is the rare association between these two autoimmune
Autor:
A. T. R. Axon, Debongnej C Donnaym, G. N. J. Tytgat, J. F. W. M. Bartelsman, E. René, R. Verdon, C. Rozé, T. Vallot, S. Matheron, C. Leport, C. Marche, Y. Van Laethem, P. Hermans, N. Clumeck, J. L. Van Laethem, N. Bourgeois, M. Gelin, F. Jacobs, F. Rickaert, J. Van De Stadt, A. Van Gossum, P. Vereerstraeten, M. Adler, G. B. McDonald, Fred Silverstein, N. G. Berg, Ph. Delmotte, J. Petermans, A. Mutsers, Th. Degrez, J. de Halleux, J. C. Debongnie, R. Fiasse, P. Mainguet, Y. Thirapathi, J. D. de Korwin, M. F. Blech, C. Rossit, M. C. Conroy, P. Hartemann, J. C. Burdin, J. Schmitt, S. Van Avermaet, S. Debeuckelaere, L. Du Ville, P. Potvin, G. Devis, D. Urbain, J. Jeanmart, M. Lemone, A. Kiromera, D. Van Daele, S. Saikali, S. De Wit, O. Thys, P. Hoang, D. P. Jewell, A. Vandelli, G. Cariani, G. Bonora, T. Lenzi, G. Fontana, J. H. Wandall, D. Alnor-Hansen, E. Hage, C. Garcéa Reinoso, F. Saez-Royuela, Guerrero M. Fernandez, Cubero JC. Porres, Campos C. González, C. Spiessens, P. de Witte, K. Geboes, J. Lemli, M. H. de Baets, G. C. Cook, J. C. Debongne, A. Jouret, J. Haot, A. Russo, G. Aprile, A. Magnano, M. Delmée, N. ctors, R. De Vos, K. eboes, P. utgeerts, V. esmet, G. antrappen, S. Motte, J. M. Dumonceau, J. Deviere, M. Baize, J. P. Thys, E. Serruys, M. Cremer, E De Koster, JF Nyst, Y Glupczynski, C Deprez, M Deltenre, P. Bechi, R. Dei, A. Amorosi, D. Pantalone, F. Pucciani, A. Di Napoli, R. Petrino, M. Boero, A. Morgando, R. Piglia, L. Chiandussi, E. Bologna, M. Stroppiana, S. Peyre, R. Rizzi, M. Bangera, C. Sateqna-Buidetti, B. Ramdani, V. Lamy, D. Famerée, J. Cappelli, R. Moisse, B. Gobert, M. C. Bene, G. Faure, JP Benhamou, J I Wyatt, F. Méqraud, M. P. Brassens-Rabbé, M. Albenque, C. Nejjari, B. J. Rathbone, G. Gasbarrini, S. Pretolani, N. Careddu, D. Cilia, P. Acampora, E. Brocchi, F. Bonvicini, P. Malfertheiner, N. Ectors, Carmelo Scarpignato, M. Deltenre, Y. Glupczynski, E. De Koster, JF. Nyst, J. Otero, R. F. Dondelinger, J. C. Kurdziel, P. Goffette, A. N. Dardenne, J. Pringot, P. Van Gansbeke, B. Lalmand, A. Grassart, J. Struyven, PJ Valette, P. Brandtzaeg, T. S. Halstensen, L. Helgeland, K. Kett, C. Cuvelier, P. P. Jewell, Sander J. H. van Deventer, Sandra A. Radema, Guido N. J. Tytgat, M. de Reuck, R. Potvliege, A. Burette, C. Deprez, C. Van Den Borre, H. Goossens, M. Verhas, L. Bourdeaux, D. DeVos, T. Devreker, S. Goutier, C. Cpttone, G. Disclafani, G. Genova, S. Romeo, P. Bazan, C Garcéa Reinoso, F Saez-Royuela, C González Campos, M. J. Struelens, C. Nonhoff, A. Maas, F. Rost, G. Gay, S. Delmotte
Publikováno v:
Acta Endoscopica. 20:153-216
Publikováno v:
Journal of Endocrinological Investigation. 13:317-326
A case of ectopic ACTH syndrome with intermittent secretion in a 72-yr-old woman is described. Plasma and urinary cortisol levels were obtained at frequent intervals for a period of more than 10 months and varied erratically from the normal range to
Publikováno v:
Journal belge de radiologie. 81(1)
Intraductal papillary-mucinous tumor of the pancreas (IPMT) is an uncommon entity, defined as an intraductal papillary proliferation of mucin-producing epithelial cells. Since the original description of the disease by Ohhashi in 1982, the definition
Autor:
J. Van De Stadt, Michel Baize, Günter Klöppel, M Devière, F. Rickaert, Michel Cremer, Michel Gelin, Camille Azar
Publikováno v:
Gut. 39(3)
BACKGROUND/AIM: The clinical presentation, pancreatographic findings, and outcome of patients with intraductal papillary mucinous tumours have not been reported in a large patient series in the English literature. This study reviewed 32 patients diag