Search Results - "Poulain, Stéphanie"

MYD88 L265P mutation in Waldenstrom macroglobulinemia by Poulain, Stéphanie, Roumier, Christophe, Decambron, Audrey, Renneville, Aline, Herbaux, Charles, Bertrand, Elisabeth, Tricot, Sabine, Daudignon, Agnès, Galiègue-Zouitina, Sylvie, Soenen, Valerie, Theisen, Olivier, Grardel, Nathalie, Nibourel, Olivier, Roche-Lestienne, Catherine, Quesnel, Bruno, Duthilleul, Patrick, Preudhomme, Claude, Leleu, Xavier

“…Mutation of the MYD88 gene has recently been identified in activated B-cell–like diffuse cell lymphoma and enhanced Janus kinase/signal transducer and…”
Get full text

TP53 Mutation and Its Prognostic Significance in Waldenstrom's Macroglobulinemia by Poulain, Stéphanie, Roumier, Christophe, Bertrand, Elisabeth, Renneville, Aline, Caillault-Venet, Aurélie, Doye, Emmanuelle, Geffroy, Sandrine, Sebda, Sheherazade, Nibourel, Olivier, Nudel, Morgane, Herbaux, Charles, Renaud, Loic, Tomowiak, Cécile, Guidez, Stéphanie, Tricot, Sabine, Roche-Lestienne, Catherine, Quesnel, Bruno, Preudhomme, Claude, Leleu, Xavier

“…is a tumor-suppressor gene that functions as a regulator influencing cellular responses to DNA damage, and alterations are associated with pejorative outcome…”
Get full text

High frequency of clonal hematopoiesis in Erdheim-Chester disease by Cohen Aubart, Fleur, Roos-Weil, Damien, Armand, Marine, Marceau-Renaut, Alice, Emile, Jean-François, Duployez, Nicolas, Charlotte, Frédéric, Poulain, Stéphanie, Lhote, Raphael, Hélias-Rodzewicz, Zofia, Della-Valle, Véronique, Bernard, Olivier, Maloum, Karim, Nguyen-Khac, Florence, Donadieu, Jean, Amoura, Zahir, Abdel-Wahab, Omar, Haroche, Julien

“…Erdheim-Chester disease (ECD) is a clonal hematopoietic disorder characterized by the accumulation of foamy histiocytes within organs (in particular, frequent…”
Get full text

Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia by Poulain, Stéphanie, Roumier, Christophe, Venet-Caillault, Aurélie, Figeac, Martin, Herbaux, Charles, Marot, Guillemette, Doye, Emmanuelle, Bertrand, Elisabeth, Geffroy, Sandrine, Lepretre, Frédéric, Nibourel, Olivier, Decambron, Audrey, Boyle, Eileen Mary, Renneville, Aline, Tricot, Sabine, Daudignon, Agnès, Quesnel, Bruno, Duthilleul, Patrick, Preudhomme, Claude, Leleu, Xavier

“…Whole-genome sequencing has revealed MYD88 L265P and CXCR4 mutations (CXCR4(mut)) as the most prevalent somatic mutations in Waldenström macroglobulinemia…”
Get full text

Guideline for the diagnosis, treatment and response criteria for Bing-Neel syndrome by Minnema, Monique C, Kimby, Eva, D'Sa, Shirley, Fornecker, Luc-Matthieu, Poulain, Stéphanie, Snijders, Tom J, Kastritis, Efstathios, Kremer, Stéphane, Fitsiori, Aikaterini, Simon, Laurence, Davi, Frédéric, Lunn, Michael, Castillo, Jorge J, Patterson, Christopher J, Le Garff-Tavernier, Magali, Costopoulos, Myrto, Leblond, Véronique, Kersten, Marie-José, Dimopoulos, Meletios A, Treon, Steven P

“…Bing Neel syndrome is a rare disease manifestation of Waldenström's macroglobulinemia that results from infiltration of the central nervous system by malignant…”
Get full text

Germline PAX5 mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia by Duployez, Nicolas, Jamrog, Laura A., Fregona, Vincent, Hamelle, Camille, Fenwarth, Laurène, Lejeune, Sophie, Helevaut, Nathalie, Geffroy, Sandrine, Caillault, Aurélie, Marceau-Renaut, Alice, Poulain, Stéphanie, Roche-Lestienne, Catherine, Largeaud, Laetitia, Prade, Naïs, Dufrechou, Stéphanie, Hébrard, Sylvie, Berthon, Céline, Nelken, Brigitte, Fernandes, José, Villenet, Céline, Figeac, Martin, Gerby, Bastien, Delabesse, Eric, Preudhomme, Claude, Broccardo, Cyril

“…[Display omitted]…”
Get full text

Bendamustine plus rituximab in newly‐diagnosed Waldenström macroglobulinaemia patients. A study on behalf of the French Innovative Leukaemia Organization (FILO) by Laribi, Kamel, Poulain, Stéphanie, Willems, Lise, Merabet, Fatiha, Le Calloch, Ronan, Eveillard, Jean R., Herbaux, Charles, Roos‐Weil, Damien, Chaoui, Driss, Roussel, Xavier, Tricot, Sabine, Dupuis, Jehan, Dartigeas, Caroline, Bareau, Benoit, Bene, Marie C., Baugier de Materre, Alix, Leblond, Véronique

Get full text

MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome by Poulain, Stéphanie, Boyle, Eileen M., Roumier, Christophe, Demarquette, Hélène, Wemeau, Mathieu, Geffroy, Sandrine, Herbaux, Charles, Bertrand, Elisabeth, Hivert, Bénédicte, Terriou, Louis, Verrier, Albert, Pollet, Jean Paul, Maurage, Claude Alain, Onraed, Brigitte, Morschhauser, Franck, Quesnel, Bruno, Duthilleul, Patrick, Preudhomme, Claude, Leleu, Xavier

“…Summary Bing‐Neel syndrome (BNS), a rare neurological syndrome associated with Waldenström macroglobulinaemia (WM), is a direct involvement of the central…”
Get full text

BH3 profiling identifies ruxolitinib as a promising partner for venetoclax to treat T-cell prolymphocytic leukemia by Herbaux, Charles, Kornauth, Christoph, Poulain, Stéphanie, Chong, Stephen J.F., Collins, Mary C., Valentin, Rebecca, Hackett, Liam, Tournilhac, Olivier, Lemonnier, François, Dupuis, Jehan, Daniel, Adrien, Tomowiak, Cecile, Laribi, Kamel, Renaud, Loïc, Roos-Weil, Damien, Rossi, Cedric, Van Den Neste, Eric, Leyronnas, Cecile, Merabet, Fatiha, Malfuson, Jean Valère, Tiab, Mourad, Ysebaert, Loïc, Ng, Samuel, Morschhauser, Franck, Staber, Philipp B., Davids, Matthew S.

“…Conventional therapies for patients with T-cell prolymphocytic leukemia (T-PLL), such as cytotoxic chemotherapy and alemtuzumab, have limited efficacy and…”
Get full text

Rationale for the combination of venetoclax and ibrutinib in T-prolymphocytic leukemia by Kornauth, Christoph, Herbaux, Charles, Boidol, Bernd, Guillemette, Chantal, Caron, Patrick, Mayerhöfer, Marius E, Poulain, Stéphanie, Tournilhac, Olivier, Pemovska, Tea, Chong, Stephen J F, Van der Kouwe, Emiel, Kazianka, Lukas, Hopfinger, Georg, Heintel, Daniel, Jäger, Roland, Raderer, Markus, Jäger, Ulrich, Simonitsch-Klupp, Ingrid, Sperr, Wolfgang R, Kubicek, Stefan, Davids, Matthew S, Staber, Philipp B

Get full text

Efficacy of ibrutinib in the treatment of Bing–Neel syndrome by Cabannes‐Hamy, Aurélie, Lemal, Richard, Goldwirt, Lauriane, Poulain, Stéphanie, Amorim, Sandy, Pérignon, Renan, Berger, Juliette, Brice, Pauline, De Kerviler, Eric, Bay, Jacques‐Olivier, Sauvageon, Helene, Beldjord, Kheira, Mourah, Samia, Tournilhac, Olivier, Thieblemont, Catherine

Get full text

Continuous MYD88 Activation Is Associated With Expansion and Then Transformation of IgM Differentiating Plasma Cells by Ouk, Catherine, Roland, Lilian, Gachard, Nathalie, Poulain, Stéphanie, Oblet, Christelle, Rizzo, David, Saintamand, Alexis, Lemasson, Quentin, Carrion, Claire, Thomas, Morgane, Balabanian, Karl, Espéli, Marion, Parrens, Marie, Soubeyran, Isabelle, Boulin, Mélanie, Faumont, Nathalie, Feuillard, Jean, Vincent-Fabert, Christelle

“…Activating mutations of ( being the far most frequent) are found in most cases of Waldenström macroglobulinemia (WM) as well as in various aggressive B-cell…”
Get full text

Absence of CXCR4 mutations but high incidence of double mutant in CD79A/B and MYD88 in primary central nervous system lymphoma by Poulain, Stéphanie, Boyle, Eileen M., Tricot, Sabine, Demarquette, Hélène, Doye, Emmanuelle, Roumier, Christophe, Duthilleul, Patrick, Preudhomme, Claude, Maurage, Claude Alain, Morschhauser, Franck

Get full text

The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots by Lazarian, Grégory, Leroy, Bernard, Theves, Floriane, Hormi, Myriam, Letestu, Rémi, Eclache, Virginie, Tueur, Giulia, Ameur, Adam, Bidet, Audrey, Cornillet-Lefebvre, Pascale, Davi, Frédéric, Delabesse, Eric, Estienne, Marie-Hélène, Etancelin, Pascaline, Kosmider, Olivier, Laibe, Sophy, Muller, Marc, Nadal, Nathalie, Naguib, Dina, Pastoret, Cédric, Poulain, Stéphanie, Sujobert, Pierre, Veronese, Lauren, Imache, Samia, Lefebvre, Valérie, Cymbalista, Florence, Baran-Marszak, Fanny, Soussi, Thierry

“…TP53 aberrations are a major predictive factor of resistance to chemoimmunotherapy in chronic lymphocytic leukemia (CLL), and an assessment of them before each…”
Get full text

Characterisation of a new clinical presentation of chronic lymphocytic leukaemia: symptomatic bronchial involvement, a study from the FILO group by Nudel, Morgane, Baran‐Marszak, Fanny, Bossard, Jean‐Baptiste, Dubois, Romain, Dapvril, Héloïse, Dupuis, Jehan, Laribi, Kamel, Bay, Jacques‐Olivier, Tomowiak, Cécile, Dreyfus, Brigitte, Lepretre, Stéphane, Demarquette, Hélène, Wallyn, Frédéric, Wemeau, Lidwine, Wemeau, Mathieu, Poulain, Stéphanie, Morschhauser, Franck, Cymbalista, Florence, Herbaux, Charles

Get full text

Working Toward a Genomic Prognostic Classification of Waldenström Macroglobulinemia by Magierowicz, Marion, Pharm D, Tomowiak, Cécile, MD, Leleu, Xavier, MD, PhD, Poulain, Stéphanie, Pharm D, PhD

“…Waldenström macroglobulinemia is a rare indolent B-cell lymphoma. Whole-exome sequencing studies have improved our knowledge of the Waldenström…”
Get full text

Mast cell density and its clinical relevance in Waldenström's macroglobulinemia by Lemal, Richard, Poulain, Stéphanie, Ledoux‐Pilon, Albane, Veronese, Lauren, Tchirkov, Andrei, Lebecque, Benjamin, Tassin, Thomas, Bay, Jacques‐Olivier, Charlotte, Frédéric, Nguyen‐Khac, Florence, Berger, Marc, Godfraind, Catherine, Ysebaert, Loïc, Davi, Frédéric, Pereira, Bruno, Leblond, Véronique, Hermine, Olivier, Guièze, Romain, Pagès, Franck, Tournilhac, Olivier

“…The presence of numerous mast cells (MCs) mixed with tumor cells in the bone marrow (BM) is a hallmark of the diagnosis of Waldenström's macroglobulinemia…”
Get full text

Lenalidomide is safe and active in Waldenström macroglobulinemia by Fouquet, Guillemette, Guidez, Stéphanie, Petillon, Marie‐Odile, Louni, Chanaz, Ohyba, Bella, Dib, Malek, Poulain, Stéphanie, Herbaux, Charles, Martin, Audrey, Thielemans, Béatrice, Brice, Pauline, Choquet, Sylvain, Bakala, Jana, Bories, Claire, Demarquette, Hélène, Nudel, Morgane, Tournilhac, Olivier, Arnulf, Bertrand, LeGouill, Steven, Morel, Pierre, Banos, Anne, Karlin, Lionel, Salles, Gilles, Leblond, Véronique, Leleu, Xavier

“…Lenalidomide is manageable and effective in multiple myeloma, particularly in elderly patients. Surprisingly, the combination of lenalidomide with rituximab…”
Get full text

Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia by Poulain, Stéphanie, Roumier, Christophe, Galiègue‐Zouitina, Sylvie, Daudignon, Agnès, Herbaux, Charles, Aiijou, Rachid, Lainelle, Amélie, Broucqsault, Natacha, Bertrand, Elisabeth, Manier, Salomon, Renneville, Aline, Soenen, Valérie, Tricot, Sabine, Roche‐Lestienne, Catherine, Duthilleul, Patrick, Preudhomme, Claude, Quesnel, Bruno, Morel, Pierre, Leleu, Xavier

“…SNP array (SNPa) was developed to detect copy number alteration (CNA) and loss of heterozygosity (LOH) without copy number changes, CN‐LOH. We aimed to…”
Get full text

Profuse telangiectasias in an immunocompetent patient misleading presentation revealing a hepatosplenic‐Tγδ‐cell lymphoma by Diarra, Ava, Carpentier, Benjamin, Dubois, Romain, Poulain, Stéphanie, Klapisz, Leo, Terriou, Louis, Farhat, Meryem‐Maud

“…Here we present the case of an hepato‐splenic‐Tγδ‐cell lymphoma interestingly occurring in a non‐immunocompromised patient, with profuse telangiectasias giving…”
Get full text