Хайлтын үр дүнгүүд - Decamp, Matthieu

High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B -н Colson, Cindy, Decamp, Matthieu, Gruchy, Nicolas, Coudray, Nadia, Ballandonne, Céline, Bracquemart, Claire, Molin, Arnaud, Mittre, Hervé, Takatani, Rieko, Jüppner, Harald, Kottler, Marie-Laure, Richard, Nicolas

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USAID Associated with Myeloid Neoplasm and VEXAS Syndrome: Two Differential Diagnoses of Suspected Adult Onset Still’s Disease in Elderly Patients -н Delplanque, Marion, Aouba, Achille, Hirsch, Pierre, Fenaux, Pierre, Graveleau, Julie, Malard, Florent, Roos-Weil, Damien, Belfeki, Nabil, Drevon, Louis, Oganesyan, Artem, Groh, Matthieu, Mahévas, Matthieu, Razanamahery, Jerome, Maigne, Gwenola, Décamp, Matthieu, Miranda, Sébastien, Quemeneur, Thomas, Rossignol, Julien, Sailler, Laurent, Sébert, Marie, Terriou, Louis, Sevoyan, Anna, Hakobyan, Yervand, Georgin-Lavialle, Sophie, Mekinian, Arsène

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Myeloid malignancies with translocation t(4;12)(q11‐13;p13): molecular landscape, clonal hierarchy and clinical outcomes -н Parinet, Vincent, Chapiro, Elise, Bidet, Audrey, Gaillard, Baptiste, Maarek, Odile, Simon, Laurence, Lefebvre, Christine, Defasque, Sabine, Mozziconacci, Marie‐Joelle, Quinquenel, Anne, Decamp, Matthieu, Lifermann, François, Ali‐Ammar, Nadia, Maillon, Agathe, Baron, Marine, Martin, Mélanie, Struski, Stéphanie, Penther, Dominique, Micol, Jean‐Baptiste, Auger, Nathalie, Bilhou‐Nabera, Chrystèle, Martignoles, Jean‐Alain, Tondeur, Sylvie, Nguyen‐Khac, Florence, Hirsch, Pierre, Roos‐Weil, Damien

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