Schechter AN - Search Results

1

Oneal PA, Gantt NM, Schwartz JD, Bhanu NV, Lee YT, Moroney JW, Reed CH, Schechter AN, Luban NL, Miller JL. Oneal PA, et al. Among authors: schechter an. Blood. 2006 Sep 15;108(6):2081-6. doi: 10.1182/blood-2006-04-015859. Epub 2006 May 30. Blood. 2006. PMID: 16735596 Free PMC article.

2

DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation.

Elion J, Berg PE, Lapouméroulie C, Trabuchet G, Mittelman M, Krishnamoorthy R, Schechter AN, Labie D. Elion J, et al. Among authors: schechter an. Blood. 1992 Feb 1;79(3):787-92. Blood. 1992. PMID: 1346253 Free article.

3

Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reaction.

Huang SZ, Rodgers GP, Zeng FY, Zeng YT, Schechter AN. Huang SZ, et al. Among authors: schechter an. Blood. 1991 Nov 1;78(9):2433-7. Blood. 1991. PMID: 1932755 Free article.

4

Levels of fetal hemoglobin necessary for treatment of sickle cell disease.

Noguchi CT, Rodgers GP, Serjeant G, Schechter AN. Noguchi CT, et al. Among authors: schechter an. N Engl J Med. 1988 Jan 14;318(2):96-9. doi: 10.1056/NEJM198801143180207. N Engl J Med. 1988. PMID: 2447498 Review. No abstract available.

5

Trans-activation of human globin genes by HTLV-I tax1.

Fox HB, Gutman PD, Dave HP, Cao SX, Mittelman M, Berg PE, Schechter AN. Fox HB, et al. Among authors: schechter an. Blood. 1989 Dec;74(8):2749-54. Blood. 1989. PMID: 2819244 Free article.

6

Is there a role for selective vasodilation in the management of sickle cell disease?

Rodgers GP, Roy MS, Noguchi CT, Schechter AN. Rodgers GP, et al. Among authors: schechter an. Blood. 1988 Mar;71(3):597-602. Blood. 1988. PMID: 3345339 Free article. Clinical Trial.

7

Electron microscopic studies of the intracellular polymerization of sickle hemoglobin.

Acquaye C, Blanchette-Mackie EJ, Reindorf C, Edelstein S, Schechter AN. Acquaye C, et al. Among authors: schechter an. Blood Cells. 1988;13(3):359-76. Blood Cells. 1988. PMID: 3382746

8

Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes.

Brittenham GM, Schechter AN, Noguchi CT. Brittenham GM, et al. Among authors: schechter an. Blood. 1985 Jan;65(1):183-9. Blood. 1985. PMID: 3965046 Free article.

9

5-Azacytidine increases gamma-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia.

Ley TJ, DeSimone J, Noguchi CT, Turner PH, Schechter AN, Heller P, Nienhuis AW. Ley TJ, et al. Among authors: schechter an. Blood. 1983 Aug;62(2):370-80. Blood. 1983. PMID: 6191799 Free article.

10

Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease.

Maier-Redelsperger M, Noguchi CT, de Montalembert M, Rodgers GP, Schechter AN, Gourbil A, Blanchard D, Jais JP, Ducrocq R, Peltier JY, et al. Maier-Redelsperger M, et al. Among authors: schechter an. Blood. 1994 Nov 1;84(9):3182-8. Blood. 1994. PMID: 7524767 Free article.

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