Go with the Flow

被引：1
作者：
Steinberg, Martin H. [1 ]
机构：
[1] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
来源：
NEW ENGLAND JOURNAL OF MEDICINE | 2017年 / 376卷 / 05期
关键词：
SICKLE-CELL-DISEASE; FETAL-HEMOGLOBIN; ENDOTHELIUM; HYDROXYUREA; ADHERENCE; ANEMIA;
D O I：
10.1056/NEJMe1615651
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：485 / 487
页数：3
相关论文
共 11 条
[1]   Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease [J].
Ataga, K. I. ;
Kutlar, A. ;
Kanter, J. ;
Liles, D. ;
Cancado, R. ;
Friedrisch, J. ;
Guthrie, T. H. ;
Knight-Madden, J. ;
Alvarez, O. A. ;
Gordeuk, V. R. ;
Gualandro, S. ;
Colella, M. P. ;
Smith, W. R. ;
Rollins, S. A. ;
Stocker, J. W. ;
Rother, R. P. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (05) :429-439
[2]   Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders [J].
Bauer, Daniel E. ;
Kamran, Sophia C. ;
Orkin, Stuart H. .
BLOOD, 2012, 120 (15) :2945-2953
[3]   National institutes of health consensus development conference statement: Hydroxyurea treatment for sickle cell disease [J].
Brawley, Otis W. ;
Cornelius, Llewellyn J. ;
Edwards, Linda R. ;
Gamble, Vanessa Northington ;
Green, Bettye L. ;
Inturrisi, Charles ;
James, Andra H. ;
Laraque, Danielle ;
Mendez, Magda ;
Montoya, Carolyn J. ;
Pollock, Brad H. ;
Robinson, Lawrence ;
Scholnik, Aaron P. ;
Schori, Melissa .
ANNALS OF INTERNAL MEDICINE, 2008, 148 (12) :932-+
[4]   Outcomes of Gene Therapy for Severe Sickle Disease and Beta-Thalassemia Major Via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex Vivo with a Lentiviral Beta AT87Q-Globin Vector [J].
Cavazzana, Marina ;
Ribeil, Jean-Antoine ;
Payen, Emmanuel ;
Suarez, Felipe ;
Beuzard, Yves ;
Touzot, Fabien ;
Cavallesco, Resy ;
Lefrere, Francois ;
Chretien, Stany ;
Bourget, Philippe ;
Monpoux, Fabrice ;
Pondarre, Corinne ;
Neven, Benedicte ;
Schmidt, Manfred ;
von Kalle, Christof ;
Kuypers, Frans A. ;
Sandler, Laura ;
Soni, Sandeep ;
Hermine, Olivier ;
Blanche, Stephane ;
De Montalembert, Mariane ;
Hacien-Bey-Abina, Salima ;
Leboulch, Philippe .
BLOOD, 2015, 126 (23)
[5]   Hydroxyurea and sickle cell anemia - Clinical utility of a myelosuppressive ''switching'' agent [J].
Charache, S ;
Barton, FB ;
Moore, RD ;
Terrin, ML ;
Steinberg, MH ;
Dover, GJ ;
Ballas, SK ;
McMahon, RP ;
Castro, O ;
Orringer, EP ;
Jones, S ;
Strayhorn, D ;
Rosse, W ;
Phillips, G ;
Peace, D ;
JohnsonTelfair, A ;
Milner, P ;
Kutlar, A ;
Tracy, A ;
Allen, GE ;
Moshang, J ;
Steinberg, M ;
Anderson, A ;
Sabahi, V ;
Pegelow, C ;
Temple, D ;
Case, E ;
Harrell, R ;
Embury, S ;
Schmidt, B ;
Koshy, M ;
TalischyZahed, N ;
Dorn, L ;
Pendarvis, G ;
McGee, M ;
Telfer, M ;
Davis, A ;
Finke, H ;
Perlin, E ;
Siteman, J ;
Gascon, P ;
diPaolo, P ;
Gargiulo, S ;
Eckman, J ;
Bailey, JH ;
Platt, A ;
Waller, L ;
Ramirez, G ;
Knors, V ;
Hernandez, S .
MEDICINE, 1996, 75 (06) :300-326
[6]   Cardiovascular complications and risk of death in sickle-cell disease [J].
Gladwin, Mark T. .
LANCET, 2016, 387 (10037) :2565-2574
[7]   ERYTHROCYTE ADHERENCE TO ENDOTHELIUM IN SICKLE-CELL-ANEMIA - A POSSIBLE DETERMINANT OF DISEASE SEVERITY [J].
HEBBEL, RP ;
BOOGAERTS, MAB ;
EATON, JW ;
STEINBERG, MH .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 302 (18) :992-995
[8]   Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes [J].
Kato, Gregory J. ;
Gladwin, Mark T. ;
Steinberg, Martin H. .
BLOOD REVIEWS, 2007, 21 (01) :37-47
[9]   P-selectin mediates the adhesion of sickle erythrocytes to the endothelium [J].
Matsui, NM ;
Borsig, L ;
Rosen, SD ;
Yaghmai, M ;
Varki, A ;
Embury, SH .
BLOOD, 2001, 98 (06) :1955-1962
[10]   Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin [J].
Ngo, Duyen A. ;
Aygun, Banu ;
Akinsheye, Idowu ;
Hankins, Jane S. ;
Bhan, Ishir ;
Luo, Hong Y. ;
Steinberg, Martin H. ;
Chui, David H. K. .
BRITISH JOURNAL OF HAEMATOLOGY, 2012, 156 (02) :259-264
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