Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Henkinbrant, A."'
Autor:
Pierre Wattiau, Eva Boldisova, Rudolf Toman, Marjan Van Esbroeck, Sophie Quoilin, Samia Hammadi, Hervé Tissot-Dupont, Didier Raoult, Jean-Marie Henkinbrant, Mieke Van Hessche, David Fretin
Publikováno v:
Emerging Infectious Diseases, Vol 17, Iss 12, Pp 2368-2369 (2011)
Externí odkaz:
https://doaj.org/article/1b4c391f75e64d53862ddee6ac338285
Publikováno v:
Acta Clinica Belgica. 50:291-296
SummaryThe authors report an observation of Wegener’s granulomatosis with pulmonary, bronchial, renal, cutaneous and sinusal involvement. Five years ago, the patient was referred to us because of bilateral diffuse pulmonary infiltrates of unknown o
Autor:
Sophie Quoilin, Jean-Marie Henkinbrant, Eva Boldisova, Hervé Tissot-Dupont, Rudolf Toman, Marjan Van Esbroeck, Didier Raoult, David Fretin, Mieke Van Hessche, Pierre Wattiau, Samia Hammadi
Publikováno v:
Emerging Infectious Diseases
Emerging Infectious Diseases, Vol 17, Iss 12, Pp 2368-2369 (2011)
Emerging Infectious Diseases, Vol 17, Iss 12, Pp 2368-2369 (2011)
To the Editor: Recent outbreaks of Q fever in the Netherlands and the United Kingdom raised public awareness about this ubiquitous bacterial disease known for decades to circulate worldwide (1–4). The disease, which ranges from a self-recovering in
Autor:
Jean-Pol d'Odemont, Ivan Philippart, Nicole Nolard, Jacques Hamels, Albert Henkinbrant, Jacques Fastrez, Max Lonneux
Publikováno v:
Journal of Allergy and Clinical Immunology. 95:1047-1049
Autor:
M.-A. Polet, J P D'Odemont, F. Breuskin, A. Henkinbrant, P. Van Eeckhout, J Fastrez, J. Dorzee
Publikováno v:
Acta clinica Belgica. 58(4)
Wegener’s disease (WG) is a systemic disease characterized histologically by necrotizing granulomatous inflammation and vasculitis involving small arteries, veins and capillaries (Klinger 1931, Wegener 1936, 1939). The mean age of onset is 40 (1, 2
Publikováno v:
The Journal of allergy and clinical immunology. 95(5 Pt 1)
[Wegener's granulomatosis: clinical, radiological and diagnostic characteristics. Apropos of a case]
Publikováno v:
Acta clinica Belgica. 50(5)
The authors report an observation of Wegener's granulomatosis with pulmonary, bronchial, renal, cutaneous and sinusal involvement. Five years ago, the patient was referred to us because of bilateral diffuse pulmonary infiltrates of unknown origin. A
Publikováno v:
Revue des maladies respiratoires. 10(1)
Publikováno v:
Acta gastro-enterologica Belgica. 53(3)
The authors describe a major pancreatic lipomatous infiltration, causing a "pseudo-hypertrophy" of the pancreas, in a 70-year-old man. This lesion was responsible of a hyperechogenic area at ultrasonography and of an empty pancreatic bed ("vanishing
Autor:
A. Henkinbrant, W. Khalek
Publikováno v:
Acta Clinica Belgica. 44:3-9
SummaryThe last 105 endoscopic sphincterotomies performed between 1983 and 1987 arc evaluated and compared with the recent data of the literature. The sphincterotomy has been successful in 98 cases (93 %). The indications were: 95 cases of common bil