Zobrazeno 1 - 10
of 113
pro vyhledávání: '"J.-C. Fournet"'
Autor:
Virginie Royal, Henri Kreis, Renaud Snanoudj, C. Legendre, Marion Rabant, J.-C. Fournet, Laure-Hélène Noël, Emmanuel Morelon, Caroline Elie, C. Girardin
Publikováno v:
American Journal of Transplantation. 11:2635-2646
The specificity of chronic histological lesions induced by calcineurin inhibitors (CNI) is often questioned, but few studies have directly compared long-term lesions in renal-transplant patients who received this treatment and those who did not. We t
Autor:
Christian Sainte-Rose, F Jaubert, J C Fournet, A Lellouch-Tubiana, A Yadav, Chantal Kalifa, J E Quazza
Publikováno v:
Histopathology. 35:170-173
Aims We report a case study to highlight the occurrence of glioblastoma multiforme in an ovarian teratoma. Methods and results A 10-year-old girl presented with a left frontal lobe primitive neuroectodermal tumour which was successfully treated. Afte
Autor:
Jean-François Rahier, M S Gross-Morand, Francis Brunelle, Jean-Marie Saudubray, V Foussier, Marie-Claire Brusset, Claire Nihoul-Fékété, J.-J. Robert, Claudine Junien, Jean-Paul Bonnefont, P de Lonlay, F. Poggi-Travert, J.-C. Fournet
Publikováno v:
Journal of Clinical Investigation, Vol. 100, no. 4, p. 802-807 (1997)
Sporadic persistent hyperinsulinemic hypoglycemia of infancy (PHHI) or nesidioblastosis is a heterogeneous disorder characterized by profound hypoglycemia due to inappropriate hypersecretion of insulin. An important diagnostic goal is to distinguish
Autor:
Michel Duval, J C Fournet, Martin A. Champagne, P Brazzola, F Gauvin, J Champagne, Jean Hugues Dalle
Publikováno v:
Bone Marrow Transplantation. 36:1103-1105
Fatal diffuse capillaritis after hematopoietic stem-cell transplantation for dyskeratosis congenita despite low-intensity conditioning regimen
Publikováno v:
Arkhiv patologii. 73(4)
The Foxl-2 gene is involved in eyelid and ovary development. Mutations can lead to a shortened protein and malformations such as BPES associated or not to POF. Forkhead point mutation C134W is a marker of adult type granulosa cell tumors only. Foxl-2
Autor:
Christine Sempoux, Claire Nihoul-Fékété, Virginie Verkarre, C. Saint-Martin, P. de Lonlay, Jean-Baptiste Arnoux, Jean-François Rahier, C. Vaury, Vassili Valayannopoulos, Francis Jaubert, Yves Aigrain, C. Bellanné-Chantelot, J.-C. Fournet, S. Gobrecht, M.J. Ribeiro
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (11), pp.752. ⟨10.1136/jmg.2009.075416⟩
Journal of Medical Genetics, 2010, 47 (11), pp.752. ⟨10.1136/jmg.2009.075416⟩
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (11), pp.752. 〈10.1136/jmg.2009.075416〉
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (11), pp.752. ⟨10.1136/jmg.2009.075416⟩
Journal of Medical Genetics, 2010, 47 (11), pp.752. ⟨10.1136/jmg.2009.075416⟩
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (11), pp.752. 〈10.1136/jmg.2009.075416〉
International audience; Background: Congenital hyperinsulinism (CHI) is characterized by an over secretion of insulin by the pancreatic ƒÒ-cells. This condition is mostly caused by mutations in ABCC8 or KCNJ11 genes encoding the SUR1 and KIR6.2 sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10b896fd7edb017724e362107205abed
https://hal.archives-ouvertes.fr/hal-00557386
https://hal.archives-ouvertes.fr/hal-00557386
Publikováno v:
Annales de pathologie. 30(3)
Publikováno v:
Paediatric respiratory reviews. 7
Autor:
M.-L. Figueres, J.-C. Fournet, David Eiss, Arnaud Mejean, V. Vasiliu, Virginie Verkarre, Olivier Hélénon, O. Alenda, J. Adam
Publikováno v:
Annales de Pathologie. 31:S185-S186
Autor:
Jean Michel Correas, Marc-Olivier Timsit, Jérôme Verine, V. Vasiliu, J. Adam, Marion Rabant, Virginie Verkarre, J.-C. Fournet, Ch. Legendre
Publikováno v:
Annales de Pathologie. 31:S184-S185