Zobrazeno 1 - 10
of 227
pro vyhledávání: '"F. Sassolas"'
Publikováno v:
Archives de Pédiatrie. 15:1541-1546
Resume L’infarctus cerebral de l’enfant est encore peu connu des pediatres, car peu frequent et de diagnostic difficile. Actuellement, la therapeutique a la phase aigue repose sur les antiagregants plaquettaires de type acide acetylsalicylique, l
Autor:
S Di Filippo, Marie Célard, Roland Henaine, A. Bozio, Jean Ninet, B Semiond, F. Sassolas, François Delahaye
Publikováno v:
Heart. 92:1490-1495
Objective: To assess the changing profile of infective endocarditis in patients with congenital heart disease. Methods: All cases diagnosed from 1966 to 2001 (revised Duke criteria) were retrospectively reviewed and categorised in periods I ( Results
Autor:
V. Mialou, S. Di Filippo, M. M. Meshref, Matthias Schell, L. Chalabreysse, P. Marec Bérard, C. Bergeron, F. Sassolas, C. Chassagne
Publikováno v:
Pediatric Blood & Cancer. 42:380-383
Primary cardiac lymphoma (PCL) is a rare and usually fatal malignancy, seldom reported in children. This report describes the case of a 10-year-old boy who presented with multiple intracardiac masses which, when biopsied, proved to be small non-cleav
Autor:
S. Di Filippo, Olivier Metton, Hervé Joly, F. Sassolas, A. Bozio, Mohamed Bakloul, Roland Henaine, C. Chareyras, Jean Ninet, Magali Veyrier, Nicolas Pangaud
Publikováno v:
Archives of Cardiovascular Diseases. 107(8-9)
This study was to: 1) analyze impact of antenatal echocardiography, 2) assess pronostic factors of outcome, in neonates and infants with coarctation of aorta (COA).MethodsSingle-center analysis of clinical and echocardiographic data of fetus with sus
Publikováno v:
Surgical and Radiologic Anatomy. 21:251-254
A left retro-aortic brachiocephalic vein is a rare anatomic entity. A retrospective study was made of 5218 congenital cardiopathies treated between 1982 and 1998 in a medico-surgical department of paediatric cardiology. A left retro-aortic brachiocep
Publikováno v:
Archives de Pédiatrie. 5:785-792
Summary Infective endocarditis remains a severe, potentially lethal disease, which justifies a rigourous prevention schedule. Children with cyanotic congenital heart disease, mitroaortic valvulopathies, prosthetic valve and uncorrected ventricular se
Autor:
A. Bozio, F. Sassolas, C. Vedrinne, G. Champsaur, François Tronc, Jacques Robin, A. Curtil, Jean Ninet
Publikováno v:
European Journal of Cardio-Thoracic Surgery. 11:117-122
Objecti6e: The choice of a valve substitute remains a challenge in young patients, with numerous reports of early degeneration and calcification of biological valves in this age group. Therefore an assessment of the long-term results after mechanical
Publikováno v:
Surgical and Radiologic Anatomy. 21:10-12
La position anormale retro-aortique de la VBCG est une anomalie rare. Cette anomalie est le plus souvent retrouvee chez les patients porteurs d'une tetralogie de Fallot. Bien que cette malformation n'ait pas de repercussion physiopathologique en elle
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 15(10)
Pediatric arterial ischemic stroke (AIS) is little known by pediatricians, as it is rare and difficult to diagnose. Current therapeutic approaches include platelet aggregation inhibitors, anticoagulation using heparin or thrombolysis with rt-PA, and
Autor:
Gabriel Baron, Arnaud Theulin, Christophe Deligny, J.C. Piette, Elizabeth Villain, Nathalie Morel, L. Mouthon, Z. Amoura, P. Ravaud, J. Lebidois, Sophie Georgin-Lavialle, N. Costedoat-Chalumeau, Kateri Levesque, Damien Bonnet, M. Hamidou, Alice Maltret, Laurent Fermont, F. Barriere, P. Pezard, E. Hachulla, Olivier Fain, D. Lemercier, P. Orquevaux, G. Guettrot-Imbert, F. Sassolas
Publikováno v:
Annals of the Rheumatic Diseases. 74:102.3-103
Background Neonatal lupus syndrome (NLS) includes congenital heart block (CHB) and cardiomyopathies. Its optimal management is debated. Objectives We analyzed the mortality and morbidity of CHB, with special focus on risk factors. Methods This was a