Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pierre-Yves Lovey"'
Autor:
Paolo Salvioni Chiabotti, Bettina Bisig, Anne Cairoli, Steven D. Hajdu, Pierre-Yves Lovey, Dina Milowich, Sonia Ziadi, Renaud Du Pasquier, Jean-Philippe Brouland, Laurence de Leval
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Central nervous system involvement in Hodgkin lymphoma is extremely rare, especially in nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), which usually carries a favorable prognosis. Here we report a case of a young patient with NLPHL, who dev
Externí odkaz:
https://doaj.org/article/04a38280eb774d72b5dc66a0df79a5e1
Autor:
Paula Fernandez, Max Solenthaler, Olivier Spertini, Stephane Quarroz, Alicia Rovo, Pierre-Yves Lovey, Leda Leoncini, Sylvie Ruault-Jungblut, Mathilde D'Asaro, Olivier Schaad, Mylène Docquier, Patrick Descombes, Thomas Matthes, Swiss Cytometry Society
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49010 (2012)
BACKGROUND: The diagnosis of malignant hematologic diseases has become increasingly complex during the last decade. It is based on the interpretation of results from different laboratory analyses, which range from microscopy to gene expression profil
Externí odkaz:
https://doaj.org/article/306354b0fbf141938812d1f062f17b23
Autor:
Carlo R. Largiadèr, Thomas R. Braschler, Stefan Farese, Behrouz Mansouri Taleghani, Pierre-Yves Lovey, Heinz Hengartner, Johanna A. Kremer Hovinga, Florian Buchkremer, Erika Tarasco
Publikováno v:
Hämostaseologie. 40:S5-S14
The Hereditary TTP Registry is an international cohort study for patients with a confirmed or suspected diagnosis of hereditary thrombotic thrombocytopenic purpura (hTTP) and their family members. Hereditary TTP is an ultra-rare blood disorder (preva
Autor:
Quentin Moyon, Marc Pineton de Chambrun, Marie Gousseff, Alexis Mathian, Miguel Hie, Geoffrey Urbanski, Franco Verlicchi, Stanislas Faguer, Antoine Dossier, Jean-Christophe Lega, Sophie Riviere, David Saadoun, Julie Graveleau, Marie-Josée Lucchini-Lecomte, Christine Christides, Sylvie Le Moal, Béatrice Bibes, Giuseppe Malizia, Marc Ruivard, Gilles Blaison, Laurent Alric, Christian Agard, Martin Soubrier, Jean-François Viallard, Hervé Levesque, Georges-Etienne Rivard, Nathalie Tieulie, Arnaud Hot, Pierre-Yves Lovey, Thomas Hanslik, François Lhote, Vincent Eble, Jorge Álvarez Troncoso, Avinash Aujayeb, Paul Quentric, Dov Taieb, Fleur Cohen-Aubart, Marc Lambert, Zahir Amoura
Publikováno v:
Journal of Allergy and Clinical Immunology: In Practice
Journal of Allergy and Clinical Immunology: In Practice, 2022, 10 (11), pp.2889-2895. ⟨10.1016/j.jaip.2022.07.006⟩
Journal of Allergy and Clinical Immunology: In Practice, 2022, 10 (11), pp.2889-2895. ⟨10.1016/j.jaip.2022.07.006⟩
International audience; Background: The systemic capillary leak syndrome (SCLS), also known as Clarkson disease, is a very rare condition characterized by recurrent life-threatening episodes of vascular hyperpermeability in the presence of a monoclon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff37f7eee45f0767c8bd973b3e66e933
https://hal.science/hal-03888981
https://hal.science/hal-03888981
Autor:
Marc Pineton de Chambrun, Quentin Moyon, Stanislas Faguer, Geoffrey Urbanski, Alexis Mathian, Noémie Zucman, Marie Werner, Charles-Edouard Luyt, Franco Verlicchi, Zahir Amoura, Marie Gousseff, Wladimir Mauhin, Arnaud Hot, Jean-Christophe Lega, Marc Lambert, Sophie Riviere, Antoine Dossier, Marc Ruivard, François Lhote, Gilles Blaison, Sybille Merceron, Nathalie Zapella, Laurent Alric, Christian Agard, Mathieu Lacout, David Saadoun, Julie Graveleau, Martin Soubrier, Julien Haroche, Julien Boileau, Marie-Josee Lucchini-Lecomte, Thomas Hanslik, Christine Christides, Hervé Levesque, Aline Talasczka, Caroline Bulte, Eric Hachulla, Olivier Decaux, Romain Sonneville, Florent Ibouanga, Bertrand Arnulf, Marcel Benedit, Jean François Viallard, Nathalie Tieulie, Fadi Haddad, Bruno Moulin, Fleur Cohen-Aubert, Pierre-Yves Lovey, Sylvie le Moal, Béatrice Bibes, Georges-Etienne Rivard, Eric Rondeau, Giuseppe Malizia, Philippe Debourdeau, Pierre Abgueguen, Annick Bosseray, Jérôme Devaquet, Claire Presne, François Liferman, Nicolas Limal, Laurent Argaud, Romain Hernu, Sylvie de la Salle, Jorge Álvarez Troncoso, John Harty, Pascal Godmer, Miguel Hie, Thomas Papo, Pierre-Yves Hatron
Publikováno v:
The Journal of Allergy and Clinical Immunology. in Practice
Autor:
Johanna A, Kremer Hovinga, Thomas R, Braschler, Florian, Buchkremer, Stefan, Farese, Heinz, Hengartner, Pierre-Yves, Lovey, Carlo R, Largiadèr, Behrouz, Mansouri Taleghani, Erika, Tarasco
Publikováno v:
Hamostaseologie. 40(S 01)
The
Autor:
Jean-Philippe Brouland, Anne Cairoli, Pierre-Yves Lovey, Bettina Bisig, Laurence de Leval, Paolo Salvioni Chiabotti, Dina Milowich, Sonia Ziadi, Renaud Du Pasquier, Steven D. Hajdu
Publikováno v:
Frontiers in oncology, vol. 10, pp. 1745
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology
Frontiers in Oncology, Vol 10 (2020)
Frontiers in Oncology
Central nervous system involvement in Hodgkin lymphoma is extremely rare, especially in nodular lymphocyte predominant Hodgkin lymphoma (NLPHL), which usually carries a favorable prognosis. Here we report a case of a young patient with NLPHL, who dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82b8af7c6cd34b0153285d8db29de69d
https://serval.unil.ch/notice/serval:BIB_F7E269EA64DC
https://serval.unil.ch/notice/serval:BIB_F7E269EA64DC
Publikováno v:
Forum Médical Suisse ‒ Swiss Medical Forum.
Un patient de 51 ans, sans antecedent medico-chirurgical, se presente aux urgences pour un gonflement abdominal, des œdemes des membres inferieurs et un essoufflement en position couchee d’apparition progressive.
Autor:
Marc Pineton de Chambrun, Marie Gousseff, Wladimir Mauhin, Jean-Christophe Lega, Marc Lambert, Sophie Rivière, Antoine Dossier, Marc Ruivard, François Lhote, Gilles Blaison, Laurent Alric, Christian Agard, David Saadoun, Julie Graveleau, Martin Soubrier, Marie-Josée Lucchini-Lecomte, Christine Christides, Annick Bosseray, Hervé Levesque, Jean-François Viallard, Nathalie Tieulie, Pierre-Yves Lovey, Sylvie Le Moal, Béatrice Bibes, Giuseppe Malizia, Pierre Abgueguen, François Lifermann, Jacques Ninet, Pierre-Yves Hatron, Zahir Amoura, Arnaud Hot, Laurent Argaud, Romain Hernu, Sylvie de la Salle, Stanislas Ledochowski, Anne-Sophie Moreau, Thomas Papo, Romain Sonneville, Bruno Verdière, Sybille Merceron, Nathalie Zappella, Mickael Landais, Nicolas Limal, Damien Contou, Thomas Similowski, Alexandre Demoule, Bertrand Souweine, Julien Haroche, Julien Boileau, Bernard Lecomte, Thomas Hanslik, Antoine Vieillard-Baron, Nicolas Terzi, Caroline Bulte, Aline Talasczka, Eric Hachulla, Olivier Decaux, Florent Ibouanga, Bertrand Arnulf, Matthieu Groh, Elie Azoulay, Marcel Benedit, Assaad Maalouf, Bruno Moulin, Fleur Cohen-Aubart, Raymond Friolet, Sylvie le Moal, Micheline Pha, Georges-Etienne Rivard, Eric Rondeau, Philippe Debourdeau, Marc Puidupin, François Beloncle, Jérôme Devaquet, Claire Presne, François Liferman, Jean-Marc Mazou, Maude Andrieu, Sylvie Paulus, Yannick Fedun, Jean-Paul Mira, Jean-Herlé Raphalen, Oscar Len Abad, Hervé Devilliers, Alister Rogers, Pascal Godmer, Charles-Edouard Luyt, Alain Combes, Miguel Hie, Alexis Mathian
Publikováno v:
The American Journal of Medicine
The American Journal of Medicine, Elsevier [Commercial Publisher] 2017, 130 (10), pp.1219.e19-1219.e27. ⟨10.1016/j.amjmed.2017.05.023⟩
The American Journal of Medicine, 2017, 130 (10), pp.1219.e19-1219.e27. ⟨10.1016/j.amjmed.2017.05.023⟩
The American Journal of Medicine, Elsevier [Commercial Publisher] 2017, 130 (10), pp.1219.e19-1219.e27. ⟨10.1016/j.amjmed.2017.05.023⟩
The American Journal of Medicine, 2017, 130 (10), pp.1219.e19-1219.e27. ⟨10.1016/j.amjmed.2017.05.023⟩
International audience; Background: Monoclonal gammopathy-associated systemic capillary-leak syndrome, also known as Clarkson disease, is a rare condition characterized by recurrent life-threatening episodes of capillary hyperpermeability in the cont
Objective To evaluate the range of long term vascular manifestations of Coxiella burnetii infection. Design Cohort study in Switzerland of people affected in 1983 by the largest reported outbreak of Q fever and who were followed up 12 years later. Fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df4a64adcb53a3624916a512718af45
https://europepmc.org/articles/PMC28177/
https://europepmc.org/articles/PMC28177/