Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Jean-Christophe Fournet"'
Autor:
Roseline Thibeault, Martin Champagne, Louis de Repentigny, Jean-Christophe Fournet, Bruce Tapiero, Albert Moghrabi, Philippe Ovetchkine
Publikováno v:
Canadian Journal of Infectious Diseases and Medical Microbiology, Vol 19, Iss 2, Pp 203-205 (2008)
Few cases of Trichosporon species infection have been reported in children. The present report describes a case of fatal disseminated Trichosporon asahii infection in a child treated for relapsed leukemia. Voriconazole has previously shown promising
Externí odkaz:
https://doaj.org/article/54a3b0e2e09c4c14a0ee3f953ad79263
Autor:
Jean-Christophe Fournet, Jeanne Tran Van Nhieu, Elie-Serge Zafrani, Alice Boyez, J. Moroch, Cyrielle Robe, Karen Leroy, Yves Allory, Odette Georges, Alice Guyard, Anaïs Pujals
Publikováno v:
Virchows Archiv. 471:491-500
Formalin-fixed paraffin-embedded (FFPE) tissue blocks are widely used to identify clinically actionable molecular alterations or perform retrospective molecular studies. Our goal was to quantify degradation of DNA occurring during mid to long-term st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c37afedf0d64b7607cf51800846db216
https://doi.org/10.1007/s00428-017-2213-0
https://doi.org/10.1007/s00428-017-2213-0
Autor:
Dina J. Zand, Jeffrey A. Cleveland, Patrick M. A. Sleiman, Denise W. Metry, Lifeng Tian, Eniko Papp, Hakon Hakonarson, Nada Abdel-Magid, Cecilia E. Kim, Yiran Guo, Sandra Catalina Camacho, Elaine H. Zackai, Dong Li, Elizabeth McPherson, Jean-Christophe Fournet, Guy Vaksmann, Cyril Morisot, Olga Camacho-Vanegas, Brendan J. Keating, Maria Celeste M. Ramirez, David B. Everman, Ben Tweddale, Frederick G. Otieno, Carrie Zabel, John A. Martignetti, Cuiping Hou, Audrey M. Bernstein, Sandra K. Masur
Publikováno v:
The American Journal of Human Genetics. 92(6):1001-1007
Infantile myofibromatosis (IM) is a disorder of mesenchymal proliferation characterized by the development of nonmetastasizing tumors in the skin, muscle, bone, and viscera. Occurrence within families across multiple generations is suggestive of an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f973fceeac5e1e60209505167624ba
Autor:
Michel Duval, Martin A. Champagne, Anne-Laure Rougemont, Hulya Ozsahin, Marc Ansari, Françoise Le Deist, Jean-Christophe Fournet
Publikováno v:
Pediatric Transplantation. 16:E146-E149
PAP is a rare alveolointerstitial lung disorder characterized histologically by the intra-alveolar accumulation of eosinophilic and PAS-positive material. We observed two cases of PAP after unrelated CB hematopoietic progenitor cell transplantation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7917f6bb07bdd3eed39bb84537a8a274
https://doi.org/10.1111/j.1399-3046.2011.01487.x
https://doi.org/10.1111/j.1399-3046.2011.01487.x
Autor:
Raouf Fetni, Anne-Laure Rougemont, Stéphane Barrette, Riwa Absi, Jean-Christophe Fournet, Alexandre Montpetit, Dorothée Bouron-Dal Soglio
Publikováno v:
Human Pathology. 40:1347-1352
Since the first description of sclerosing rhabdomyosarcoma in 2000, 19 pediatric cases have been reported in the literature. However, it is debated whether sclerosing rhabdomyosarcoma represents a specific rhabdomyosarcoma entity or a variant of embr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb69feae3bc8f0eb4093ffa3c1e39dd
https://doi.org/10.1016/j.humpath.2009.01.021
https://doi.org/10.1016/j.humpath.2009.01.021
Autor:
Cybèle Bergeron, Anne-Laure Rougemont, Dorothée Bouron-Dal Soglio, Philippe Ovetchkine, Chantal Buteau, Jean-Christophe Fournet
Publikováno v:
Pediatric and Developmental Pathology. 12:390-393
Community-associated infections and especially pleural empyema due to Staphylococcus aureus are increasing worldwide. The virulence of staphylococcal strains is notably determined by different toxin expressing–genes, such as the Panton-Valentine le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3e7d4733c3a6368c0c57fce934adbee
https://doi.org/10.2350/08-09-0531.1
https://doi.org/10.2350/08-09-0531.1
Autor:
Françoise Rypens, Alexandre Montpetit, Dorothée Bouron-Dal Soglio, Anthony S. De Buys Roessingh, Anne-Laure Rougemont, Sarah Bouchard, Raouf Fetni, Jean-Christophe Fournet
Publikováno v:
American Journal of Surgical Pathology, Vol. 32, No 7 (2008) pp. 1095-1100
Neonatal cystic disorders of the lungs are a heterogeneous malformative group including giant lobar hyperinflation, congenital pulmonary airway malformations, intralobar pulmonary sequestration, and bronchogenic cyst. Here, we describe a giant cystic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76bb9ceb9a26f0e0ee8a8e1fae1a833d
https://doi.org/10.1097/pas.0b013e3181676fe7
https://doi.org/10.1097/pas.0b013e3181676fe7
Autor:
Françoise Truong, Raouf Fetni, Sawcene Hazourli, Dorothée Bouron-Dal Soglio, Josette Champagne, Luc L. Oligny, Jean-Christophe Fournet
Publikováno v:
Human Pathology. 39:292-297
Progressive transformation of germinal center (PTGC) is a pattern of lymph node reactive hyperplasia. It can also be the predominant pattern in a hyperplastic lymph node known as florid PTGC. It is characterized histologically by the expansion of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e262df5e571fa846f99ccb75041a3b0
https://doi.org/10.1016/j.humpath.2007.08.002
https://doi.org/10.1016/j.humpath.2007.08.002
Autor:
Aziz Belkadi, Bertrand Boisson, Emmanuel Laplantine, Kerry Dobbs, Gregory Hopkins, Hermann Eibel, Jean-Christophe Fournet, Sung-Yun Pai, Hart G.W. Lidov, Yuval Itan, Aurélie Cobat, Waleed Al-Herz, Luigi D. Notarangelo, Maya Chrabieh, Laurent Abel, Capucine Picard, Alain Israël, Erdyni N. Tsitsikov, Nadine Tarantino, Jean-Laurent Casanova, Melissa M. Hazen, Likun Du
Publikováno v:
Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2015, ⟨10.1084/jem.20141130⟩
Journal of Experimental Medicine, Rockefeller University Press, 2015, 〈10.1084/jem.20141130〉
The Journal of Experimental Medicine
Journal of Experimental Medicine, 2015, ⟨10.1084/jem.20141130⟩
Journal of Experimental Medicine, Rockefeller University Press, 2015, ⟨10.1084/jem.20141130⟩
Journal of Experimental Medicine, Rockefeller University Press, 2015, 〈10.1084/jem.20141130〉
The Journal of Experimental Medicine
Journal of Experimental Medicine, 2015, ⟨10.1084/jem.20141130⟩
Boisson et al. report a human homozygous mutation of HOIP, the gene encoding the catalytic component of the linear ubiquitination chain assembly complex, LUBAC. The missense alleles impair the expression of HOIP, destabilizing the LUBAC complex and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbd52fa3d4ae748a672d65b648e1fddf
https://hal-pasteur.archives-ouvertes.fr/pasteur-01158038
https://hal-pasteur.archives-ouvertes.fr/pasteur-01158038
Autor:
Josée Dubois, Laurent Garel, Jacques L. Michaud, Françoise Rypens, Andrée Grignon, Jean-Christophe Fournet
Publikováno v:
RadioGraphics. 26:811-829
Hand anomalies are difficult to diagnose and are often overlooked during prenatal ultrasonography (US). The spectrum of malformations varies from subtle finger deformities to the complete amputation of limbs. Malformations of the hand can be classifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::635d4bfe334bbf0078dba9a03f0506e0
https://doi.org/10.1148/rg.263055113
https://doi.org/10.1148/rg.263055113