Martin H. Steinberg
Martin H. Steinberg
Professor of Medicine, Boston University School of Medicine
Verified email at
Cited by
Cited by
Mortality in sickle cell disease--life expectancy and risk factors for early death
OS Platt, DJ Brambilla, WF Rosse, PF Milner, O Castro, MH Steinberg, ...
New England Journal of Medicine 330 (23), 1639-1644, 1994
Sickle cell disease
FB Piel, MH Steinberg, DC Rees
New England Journal of Medicine 376 (16), 1561-1573, 2017
CRISPR-Cas9 gene editing for sickle cell disease and β-thalassemia
H Frangoul, D Altshuler, MD Cappellini, YS Chen, J Domm, BK Eustace, ...
New England Journal of Medicine 384 (3), 252-260, 2021
Disorders of hemoglobin: genetics, pathophysiology, and clinical management
MH Steinberg, BG Forget, DR Higgs, DJ Weatherall
Cambridge University Press, 2009
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment
MH Steinberg, F Barton, O Castro, CH Pegelow, SK Ballas, A Kutlar, ...
Jama 289 (13), 1645-1651, 2003
Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes
GJ Kato, MT Gladwin, MH Steinberg
Blood reviews 21 (1), 37-47, 2007
Management of sickle cell disease
MH Steinberg
New England Journal of Medicine 340 (13), 1021-1030, 1999
Erythrocyte adherence to endothelium in sickle-cell anemia: a possible determinant of disease severity
RP Hebbel, MAB Boogaerts, JW Eaton, MH Steinberg
New England Journal of Medicine 302 (18), 992-995, 1980
Intravascular hemolysis and the pathophysiology of sickle cell disease
GJ Kato, MH Steinberg, MT Gladwin
The Journal of clinical investigation 127 (3), 750-760, 2017
Fetal hemoglobin in sickle cell anemia
I Akinsheye, A Alsultan, N Solovieff, D Ngo, CT Baldwin, P Sebastiani, ...
Blood, The Journal of the American Society of Hematology 118 (1), 19-27, 2011
Genetic signatures of exceptional longevity in humans
P Sebastiani, N Solovieff, AT DeWan, KM Walsh, A Puca, SW Hartley, ...
PloS one 7 (1), e29848, 2012
Spontaneous oxygen radical generation by sickle erythrocytes.
RP Hebbel, JW Eaton, M Balasingam, MH Steinberg
The Journal of clinical investigation 70 (6), 1253-1259, 1982
The risks and benefits of long‐term use of hydroxyurea in sickle cell anemia: a 17.5 year follow‐up
MH Steinberg, WF McCarthy, O Castro, SK Ballas, FD Armstrong, W Smith, ...
American journal of hematology 85 (6), 403-408, 2010
Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms
M Saleh, JP Vaillancourt, RK Graham, M Huyck, SM Srinivasula, ...
Nature 429 (6987), 75-79, 2004
Hydroxyurea and sickle cell anemia clinical utility of a myelosuppressive “Switching” agent
S Charache, FB Barton, RD Moore, ML Terrin, MH Steinberg, GJ Dover, ...
Medicine 75 (6), 300-326, 1996
Predicting clinical severity in sickle cell anaemia
MH Steinberg
British journal of haematology 129 (4), 465-481, 2005
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea
MH Steinberg, ZH Lu, FB Barton, ML Terrin, S Charache, GJ Dover, ...
Blood, The Journal of the American Society of Hematology 89 (3), 1078-1088, 1997
Vasculopathy in sickle cell disease: biology, pathophysiology, genetics, translational medicine and new research directions
GJ Kato, RP Hebbel, MH Steinberg, MT Gladwin
American journal of hematology 84 (9), 618, 2009
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
P Sebastiani, MF Ramoni, V Nolan, CT Baldwin, MH Steinberg
Nature genetics 37 (4), 435-440, 2005
Sickle cell anemia, the first molecular disease: overview of molecular etiology, pathophysiology, and therapeutic approaches
MH Steinberg
The Scientific World Journal 8 (1), 1295-1324, 2008
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