Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pierre, Sidon"'
Autor:
Vincent Cottin, Frédéric Lambert, Jean-François Cordier, Pierre Heimann, Dominique Bron, Pierre Sidon, Florence Roufosse
Publikováno v:
Respiration. 91:374-379
Chronic eosinophilic leukaemia associated with the FIP1L1-PDGFRA fusion gene (F/P+ CEL) is a rare cause of marked persistent hypereosinophilia, arising almost exclusively in male patients. Clinical presentations are heterogeneous with a higher incide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e51bc057c33a82aafb763bc32ee51b3b
https://doi.org/10.1159/000446076
https://doi.org/10.1159/000446076
Autor:
Pierre Sidon
Publikováno v:
La Cause Du Désir. :176
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4759784d4bc06959392f99925ef8a6a7
https://doi.org/10.3917/lcdd.105.0176
https://doi.org/10.3917/lcdd.105.0176
Autor:
Stéphanie Saxer, Pierre Sidon, John Stradling, Rudolf Speich, Elisabeth D. Hasler, Yeon-Mok Oh, Florence Roufosse, Ji Hyun Lee, Simonetta Baraldo, Marina Saetta, Jae Seung Lee, Kwang Ha Yoo, Malcolm Kohler, Yong Bum Park, Satz Mengensatzproduktion, Lisa Ayers, Nayia Petousi, Nasstasja Wassilew, Changhwan Kim, Vincent Cottin, Davide Biondini, Harald Hoffmann, Sang Do Lee, Chris D. Turnbull, Tae Hyung Kim, Lars C. Huber, Dominique Bron, Jin Hwa Lee, Ji Ye Jung, Mona Lichtblau, Chin Kook Rhee, Konrad E. Bloch, Silvia Ulrich, Berne Ferry, Young Sam Kim, Seong Yong Lim, Claire Andrejak, Elisabetta Balestro, Frédéric Lambert, Graziella Turato, Joon Beom Seo, Jean-François Cordier, Maria Enrica Tiné, Christoph Lange, Pierre Heimann, Erica Bazzan, Werner Druck Medien Ag, Seung Soo Sheen, Gina Somaini, Manuel G. Cosio
Publikováno v:
Respiration; international review of thoracic diseases. 91(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77473af16bcea7ff348813e21b964d9e
https://pubmed.ncbi.nlm.nih.gov/27300514
https://pubmed.ncbi.nlm.nih.gov/27300514
Autor:
Florence, Roufosse, Pierre, Heimann, Frédéric, Lambert, Pierre, Sidon, Dominique, Bron, Vincent, Cottin, Jean-François, Cordier
Publikováno v:
Respiration; international review of thoracic diseases. 91(5)
Chronic eosinophilic leukaemia associated with the FIP1L1-PDGFRA fusion gene (F/P+ CEL) is a rare cause of marked persistent hypereosinophilia, arising almost exclusively in male patients. Clinical presentations are heterogeneous with a higher incide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd60763e538627d534be6cb383758ecd
https://pubmed.ncbi.nlm.nih.gov/27164940
https://pubmed.ncbi.nlm.nih.gov/27164940
Autor:
Pierre Sidon
Publikováno v:
La Cause Du Désir. :80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d88cae82528075faaafc0f2a596567b8
https://doi.org/10.3917/lcdd.097.0080
https://doi.org/10.3917/lcdd.097.0080
Autor:
Hakim El Housni, Frédéric Lambert, Valérie Robin, Pierre Sidon, Barbara Dessars, Pierre Heimann
Publikováno v:
Clinical Chemistry. 52:1436-1438
We developed a quantitative and very sensitive method that combines molecular beacon (1) and locked nucleic acid (LNA) technologies (2) in a single sealed tube. We used the oncogenic somatic JAK2 V617F single-base sequence variant, observed in a broa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26606d9374ea9631a85e4b23e4b47bb5
https://doi.org/10.1373/clinchem.2006.066886
https://doi.org/10.1373/clinchem.2006.066886
Publikováno v:
Leukemia. 20(9)
The JAK2 V617F mutation is detectable at very low level in peripheral blood of healthy donors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60d3b2e0d21831fdf409f4d755aa2d0b
https://pubmed.ncbi.nlm.nih.gov/17268517
https://pubmed.ncbi.nlm.nih.gov/17268517
Autor:
Pierre Sidon
Publikováno v:
La Cause Du Désir. :51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e3472b1b9ad9d9df0aef8196c4f26b
https://doi.org/10.3917/lcdd.088.0051
https://doi.org/10.3917/lcdd.088.0051
Publikováno v:
Leukemia. 21:815-816
The JAK2 V617F mutation is detectable in granulocyte populations at greater than 2 copies per cell among individuals with myeloproliferative disorders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35a52dae831bdaf9a7814147bb0d9207
https://doi.org/10.1038/sj.leu.2404567
https://doi.org/10.1038/sj.leu.2404567