Steinberg MH - Search Results

1

The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.

Steinberg MH, McCarthy WF, Castro O, Ballas SK, Armstrong FD, Smith W, Ataga K, Swerdlow P, Kutlar A, DeCastro L, Waclawiw MA; Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia and MSH Patients' Follow-Up. Steinberg MH, et al. Am J Hematol. 2010 Jun;85(6):403-8. doi: 10.1002/ajh.21699. Am J Hematol. 2010. PMID: 20513116 Free PMC article. Clinical Trial.

2

Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.

Steinberg MH, Embury SH. Steinberg MH, et al. Blood. 1986 Nov;68(5):985-90. Blood. 1986. PMID: 3533181 Free article. Review.

3

Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene.

Steinberg MH, Embury SH. Steinberg MH, et al. Birth Defects Orig Artic Ser. 1987;23(5A):43-8. Birth Defects Orig Artic Ser. 1987. PMID: 3689929 No abstract available.

4

Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia.

Steinberg MH, Hsu H, Nagel RL, Milner PF, Adams JG, Benjamin L, Fryd S, Gillette P, Gilman J, Josifovska O, et al. Steinberg MH, et al. Am J Hematol. 1995 Mar;48(3):175-81. doi: 10.1002/ajh.2830480307. Am J Hematol. 1995. PMID: 7532353

5

Mortality in sickle cell disease. Life expectancy and risk factors for early death.

Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH, Klug PP. Platt OS, et al. Among authors: steinberg mh. N Engl J Med. 1994 Jun 9;330(23):1639-44. doi: 10.1056/NEJM199406093302303. N Engl J Med. 1994. PMID: 7993409 Free article.

6

Hydroxyurea and sickle cell anemia. Clinical utility of a myelosuppressive "switching" agent. The Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Charache S, Barton FB, Moore RD, Terrin ML, Steinberg MH, Dover GJ, Ballas SK, McMahon RP, Castro O, Orringer EP. Charache S, et al. Among authors: steinberg mh. Medicine (Baltimore). 1996 Nov;75(6):300-26. doi: 10.1097/00005792-199611000-00002. Medicine (Baltimore). 1996. PMID: 8982148 Free article. Clinical Trial.

7

Hematological effects of atypical and Cameroon beta-globin gene haplotypes in adult sickle cell anemia.

Steinberg MH, Lu ZH, Nagel RL, Venkataramani S, Milner PF, Huey L, Safaya S, Rieder RF. Steinberg MH, et al. Am J Hematol. 1998 Oct;59(2):121-6. doi: 10.1002/(sici)1096-8652(199810)59:2<121::aid-ajh4>3.0.co;2-#. Am J Hematol. 1998. PMID: 9766796 Free article.

8

Modulation of fetal hemoglobin in sickle cell anemia.

Steinberg MH. Steinberg MH. Hemoglobin. 2001 May;25(2):195-211. doi: 10.1081/hem-100104028. Hemoglobin. 2001. PMID: 11480781 Review.

9

Pathophysiology of sickle cell disease: role of cellular and genetic modifiers.

Steinberg MH, Rodgers GP. Steinberg MH, et al. Semin Hematol. 2001 Oct;38(4):299-306. doi: 10.1016/s0037-1963(01)90023-x. Semin Hematol. 2001. PMID: 11605164 Review.

10

New Views of Sickle Cell Disease Pathophysiology and Treatment.

Rosse WF, Narla M, Petz LD, Steinberg MH. Rosse WF, et al. Among authors: steinberg mh. Hematology Am Soc Hematol Educ Program. 2000:2-17. doi: 10.1182/asheducation-2000.1.2. Hematology Am Soc Hematol Educ Program. 2000. PMID: 11701532

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