Zobrazeno 1 - 10
of 226
pro vyhledávání: '"A.-M. Beaufrère"'
Autor:
A.-M. Beaufrère, Didier Lémery, Denis Gallot, Pierre Dechelotte, M. Biard, H. Laurichesse-Delmas, F. Desvignes
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 42:290-296
Fetal brain tumors are rare and have different histologies. Although the definitive diagnosis relies on the histopathology of the tumor, it is useful to distinguish the tumors potentially curable from the tumors rapidly fatal after birth. Nevertheles
Autor:
S. Pouplin, Olivier Vittecoq, Thierry Lequerré, Gilles Avenel, C. Banse, Alain Daragon, P. Rottenberg, A. Devauchelle, M. Beaufrère, M. Kozyreff
Publikováno v:
Médecine et Maladies Infectieuses. 48:S92
Introduction Les infections osteoarticulaires (IOA) peuvent reveler une endocardite infectieuse (EI). En pratique clinique hospitaliere, la recherche d’une endocardite est frequente lorsqu’un patient presente une IOA. L’objectif de cette etude
Autor:
Armour, Marc1 (AUTHOR) joanne.michou@cvsvets.com, Michou, Joanne1 (AUTHOR), Schofield, Imogen2 (AUTHOR), Borland, Karla1 (AUTHOR)
Publikováno v:
Animals (2076-2615). Oct2024, Vol. 14 Issue 19, p2756. 10p.
Publikováno v:
La Revue de Médecine Interne. 27:144-147
Resume Introduction. – L'atteinte pancreatique est une localisation exceptionnelle de la granulomatose de Wegener et merite d'etre signalee. Exegese. – Nous decrivons une observation d'une forme pseudo-tumorale de granulomatose de Wegener localis
Autor:
C. Boda, P. Dechelotte, Didier Lémery, H. Laurichesse-Delmas, A.-M. Beaufrère, V. Sapin, Denis Gallot
Publikováno v:
Gynécologie Obstétrique & Fertilité. 31:943-947
Diffuse chorioangiomatosis is a rare placental pathology characterized by multiple chorioangiomas, inducing a high risk of fetal complications, especially cardiovascular, with a risk of fetal death. The physiopathology is not clearly established but
Autor:
Didier Lémery, H. Laurichesse-Delmas, A. Martin, P. Dechelotte, A. G. Kaemmerlen, A. M. Beaufrère
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 20:612-615
We describe the features of Fowler syndrome (proliferative vasculopathy and hydrocephaly-hydranencephaly) diagnosed in the first trimester. The pregnancy with no significant family history was referred for karyotyping and ultrasound examination after
Autor:
Matteini, Francesco1,2 (AUTHOR), Cannella, Roberto1 (AUTHOR), Garzelli, Lorenzo3,4 (AUTHOR), Dioguardi Burgio, Marco3,4 (AUTHOR), Sartoris, Riccardo3,4 (AUTHOR), Brancatelli, Giuseppe1 (AUTHOR), Vilgrain, Valérie3,4 (AUTHOR), Ronot, Maxime3,4 (AUTHOR), Vernuccio, Federica1 (AUTHOR) federicavernuccio@gmail.com
Publikováno v:
Insights into Imaging. 7/18/2024, Vol. 15 Issue 1, p1-17. 17p.
Autor:
F, Desvignes, A-M, Beaufrère, M, Biard, P, Déchelotte, H, Laurichesse-Delmas, D, Lemery, D, Gallot
Publikováno v:
Journal de gynecologie, obstetrique et biologie de la reproduction. 42(3)
Fetal brain tumors are rare and have different histologies. Although the definitive diagnosis relies on the histopathology of the tumor, it is useful to distinguish the tumors potentially curable from the tumors rapidly fatal after birth. Nevertheles
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9(12)
The early mortality of Kawasaki disease is low, resulting from coronary complications, mainly aneurismal thrombosis with myocardial infarction. The aneurysmal rupture is an exceptional cause of death.We report on a six-month-old girl who died suddenl
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 20(6)
We describe the features of Fowler syndrome (proliferative vasculopathy and hydrocephaly-hydranencephaly) diagnosed in the first trimester. The pregnancy with no significant family history was referred for karyotyping and ultrasound examination after