Embury SH - Search Results

1

Oxygen-induced marrow red cell hypoplasia leading to transfusion in sickle painful crisis.

Lane PK, Embury SH, Toy PT. Lane PK, et al. Among authors: embury sh. Am J Hematol. 1988 Jan;27(1):67-8. doi: 10.1002/ajh.2830270117. Am J Hematol. 1988. PMID: 3128106

2

The incidence of painful crisis in homozygous sickle cell disease: correlation with red cell deformability.

Lande WM, Andrews DL, Clark MR, Braham NV, Black DM, Embury SH, Mentzer WC. Lande WM, et al. Among authors: embury sh. Blood. 1988 Dec;72(6):2056-9. Blood. 1988. PMID: 3196878 Free article.

3

Cellular adhesion and the endothelium: P-selectin.

Kutlar A, Embury SH. Kutlar A, et al. Among authors: embury sh. Hematol Oncol Clin North Am. 2014 Apr;28(2):323-39. doi: 10.1016/j.hoc.2013.11.007. Epub 2014 Jan 17. Hematol Oncol Clin North Am. 2014. PMID: 24589269 Review.

4

The interaction of alpha-thalassemia with sickle cell anemia.

Embury SH. Embury SH. Hemoglobin. 1988;12(5-6):509-17. doi: 10.3109/03630268808991639. Hemoglobin. 1988. PMID: 3209393

5

Heparin inhibits the flow adhesion of sickle red blood cells to P-selectin.

Matsui NM, Varki A, Embury SH. Matsui NM, et al. Among authors: embury sh. Blood. 2002 Nov 15;100(10):3790-6. doi: 10.1182/blood-2002-02-0626. Epub 2002 Jul 5. Blood. 2002. PMID: 12393591 Free article.

6

Alpha thalassemia. A modifier of sickle cell disease.

Embury SH. Embury SH. Ann N Y Acad Sci. 1989;565:213-21. doi: 10.1111/j.1749-6632.1989.tb24169.x. Ann N Y Acad Sci. 1989. PMID: 2476060 Review. No abstract available.

7

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.

8

Viral burden and disease progression in HIV-1-infected patients with sickle cell anemia.

Bagasra O, Steiner RM, Ballas SK, Castro O, Dornadula G, Embury S, Jungkind D, Bobroski L, Kutlar A, Burchott S. Bagasra O, et al. Am J Hematol. 1998 Nov;59(3):199-207. doi: 10.1002/(sici)1096-8652(199811)59:3<199::aid-ajh4>3.0.co;2-l. Am J Hematol. 1998. PMID: 9798657 Free article. Clinical Trial.

9

Hematologic malignancy in sickle cell disease: report of four cases and review of the literature.

Stricker RB, Linker CA, Crowley TJ, Embury SH. Stricker RB, et al. Among authors: embury sh. Am J Hematol. 1986 Feb;21(2):223-30. doi: 10.1002/ajh.2830210212. Am J Hematol. 1986. PMID: 3455791

10

The effect of speed of deoxygenation on the percentage of aligned hemoglobin in sickle cells. Application of differential polarization microscopy.

Mickols WE, Corbett JD, Maestre MF, Tinoco I Jr, Kropp J, Embury SH. Mickols WE, et al. Among authors: embury sh. J Biol Chem. 1988 Mar 25;263(9):4338-46. J Biol Chem. 1988. PMID: 3346250 Free article.

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