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Table of Contents

October 20, 2016; 128 (16)

BLOOD FLASHBACK

INSIDE BLOOD COMMENTARIES

REVIEW ARTICLE

HEMATOPOIESIS AND STEM CELLS

  • Perturbed hematopoiesis in mice lacking ATMIN
    Fernando Anjos-Afonso, Joanna I. Loizou, Amy Bradburn, Nnennaya Kanu, Sukhveer Purewal, Clive Da Costa, Dominique Bonnet and Axel Behrens

PLATELETS AND THROMBOPOIESIS

THROMBOSIS AND HEMOSTASIS

TRANSPLANTATION

LETTERS TO BLOOD

  • A novel TERC CR4/CR5 domain mutation causes telomere disease via decreased TERT binding
    Baris Boyraz, Courtney M. Bellomo, Mark D. Fleming, Corey S. Cutler and Suneet Agarwal
  • Validation of the CLL-IPI and comparison with the MDACC prognostic index in newly diagnosed patients
    Massimo Gentile, Tait D. Shanafelt, Davide Rossi, Luca Laurenti, Francesca R. Mauro, Stefano Molica, Giovanna Cutrona, Giuseppina Uccello, Melissa Campanelli, Ernesto Vigna, Giovanni Tripepi, Kari G. Chaffee, Sameer A. Parikh, Sabrina Bossio, Anna Grazia Recchia, Idanna Innocenti, Raffaella Pasquale, Antonino Neri, Manlio Ferrarini, Gianluca Gaidano, Robin Foà and Fortunato Morabito
  • Cytopenia levels for aiding establishment of the diagnosis of myelodysplastic syndromes
    Peter L. Greenberg, Heinz Tuechler, Julie Schanz, Guillermo Sanz, Guillermo Garcia-Manero, Francesc Solé, John M. Bennett, David Bowen, Pierre Fenaux, Francois Dreyfus, Hagop Kantarjian, Andrea Kuendgen, Alessandro Levis, Luca Malcovati, Mario Cazzola, Jaroslav Cermak, Christa Fonatsch, Michelle M. Le Beau, Marilyn L. Slovak, Otto Krieger, Michael Luebbert, Jaroslaw Maciejewski, Silvia M. M. Magalhaes, Yasushi Miyazaki, Michael Pfeilstöcker, Mikkael Sekeres, Wolfgang R. Sperr, Reinhard Stauder, Sudhir Tauro, Peter Valent, Teresa Vallespi, Arjan A. van de Loosdrecht, Ulrich Germing and Detlef Haase
  • Chronic neutrophilic leukemia in a child with a CSF3R T618I germ line mutation
    Lawrence J. Druhan, Daniel P. McMahon, Nury Steuerwald, Andrea E. Price, Amanda Lance, Jonathan M. Gerber and Belinda R. Avalos
  • Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutations
    Nour Abdulhay, Claudia Fiorini, Attila Kumánovics, Ashleigh A. Sun, Jeannette Hansen-Rejali, Karl V. Voelkerding, Sergio D. Rosenzweig, Harry R. Hill and Vijay G. Sankaran

BLOOD WORK

CONTINUING MEDICAL EDUCATION (CME) QUESTIONS