HuGE Literature Finder
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| Incidence and prognostic impact of cytogenetic aberrations in patients with systemic mastocytosis. Genes, chromosomes & cancer 2018 Jan . Naumann Nicole, Jawhar Mohamad, Schwaab Juliana, Kluger Sebastian, Lübke Johannes, Metzgeroth Georgia, Popp Henning D, Khaled Nada, Horny Hans-Peter, Sotlar Karl, Valent Peter, Haferlach Claudia, Göhring Gudrun, Schlegelberger Brigitte, Meggendorfer Manja, Hofmann Wolf-Karsten, Cross Nicholas C P, Reiter Andreas, Fabarius Ali |
| Impact of somatic and germline mutations on the outcome of systemic mastocytosis. Blood advances 2018 11 2 (21): 2814-2828. Muñoz-González Javier I, Jara-Acevedo María, Alvarez-Twose Iván, Merker Jason D, Teodosio Cristina, Hou Yanli, Henriques Ana, Roskin Krishna M, Sanchez-Muñoz Laura, Tsai Albert G, Caldas Carolina, Matito Almudena, Sánchez-Gallego J Ignacio, Mayado Andrea, Dasilva-Freire Noelia, Gotlib Jason R, Escribano Luis, Orfao Alberto, García-Montero Andrés |
| Splenomegaly, elevated alkaline phosphatase and mutations in the SRSF2/ASXL1/RUNX1 gene panel are strong adverse prognostic markers in patients with systemic mastocytosis. Leukemia 2016 Jul . Jawhar M, Schwaab J, Hausmann D, Clemens J, Naumann N, Henzler T, Horny H-P, Sotlar K, Schoenberg S O, Cross N C P, Fabarius A, Hofmann W-K, Valent P, Metzgeroth G, Reiter |
| Mastocytosis among elderly patients: A multicenter retrospective French study on 53 patients. Medicine 2016 Jun 95 (24): e3901. Rouet Audrey, Aouba Achille, Damaj Gandhi, Soucié Erinn, Hanssens Katia, Chandesris Marie-Olivia, Livideanu Cristina Bulai, Dutertre Marine, Durieu Isabelle, Grandpeix-Guyodo Catherine, Barète Stéphane, Bachmeyer Claude, Soria Angèle, Frenzel Laurent, Fain Olivier, Grosbois Bernard, de Gennes Christian, Hamidou Mohamed, Arlet Jean-Benoit, Launay David, Lavigne Christian, Arock Michel, Lortholary Olivier, Dubreuil Patrice, Hermine Olivier, Georgin-Lavialle Soph |
| Molecular profiling of myeloid progenitor cells in multi-mutated advanced systemic mastocytosis identifies KIT D816V as a distinct and late event. Leukemia 2015 May 29 (5): 1115-22. Jawhar M, Schwaab J, Schnittger S, Sotlar K, Horny H-P, Metzgeroth G, Müller N, Schneider S, Naumann N, Walz C, Haferlach T, Valent P, Hofmann W-K, Cross N C P, Fabarius A, Reiter |
| The detection of SRSF2 mutations in routinely processed bone marrow biopsies is useful in the diagnosis of chronic myelomonocytic leukemia. Human pathology 2014 Dec 45 (12): 2471-9. Federmann Birgit, Abele Manuel, Rosero Cuesta David Santiago, Vogel Wichard, Boiocchi Leonardo, Kanz Lothar, Quintanilla-Martinez Leticia, Orazi Attilio, Bonzheim Irina, Fend Fal |
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