Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea.
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M L Terrin | F. Barton | M. Steinberg | G. Dover | S. Charache | M. Terrin | M H Steinberg | G J Dover | S Charache | Z H Lu | F B Barton | Z. Lu | Z. H. Lu | Z. Lu
[1] S. Antonarakis,et al. Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[2] S. Charache,et al. Flow cytometric reticulocyte counting with thioflavin T in a clinical hematology laboratory. , 1987, Archives of pathology & laboratory medicine.
[3] Richard D Moore,et al. Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia. , 1992, Blood.
[4] M L Terrin,et al. Hydroxyurea and Sickle Cell Anemia Clinical Utility of a Myelosuppressive “Switching” Agent , 1996, Medicine.
[5] K. Betke,et al. Estimation of small percentages of foetal haemoglobin. , 1959, Nature.
[6] E Vichinsky,et al. Pain in sickle cell disease. Rates and risk factors. , 1991, The New England journal of medicine.
[7] M L Terrin,et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. , 1995, The New England journal of medicine.
[8] M. Keating,et al. The long QT syndrome. A review of recent molecular genetic and physiologic discoveries. , 1996, Medicine.
[9] T. Huisman,et al. DNA sequence variation associated with elevated fetal G gamma globin production. , 1985, Blood.
[10] N. Anagnou,et al. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait. , 1986, Blood.
[11] W. Bell,et al. Microscopic method for assaying F cell production: illustrative changes during infancy and in aplastic anemia. , 1978, Blood.
[12] R. Ware,et al. Hydroxyurea: An alternative to transfusion therapy for stroke in sickle cell anemia , 1995, American journal of hematology.
[13] J. Clegg,et al. The interaction of alpha-thalassemia and homozygous sickle-cell disease. , 1982, The New England journal of medicine.
[14] S. Zeger,et al. Longitudinal data analysis using generalized linear models , 1986 .
[15] D. Labie,et al. Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type. , 1985, The New England journal of medicine.
[16] G. Dover,et al. Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia. , 1987, Blood.
[17] A. Schechter,et al. Hematologic responses of patients with sickle cell disease to treatment with hydroxyurea. , 1990, The New England journal of medicine.
[18] D. Powars,et al. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. , 1993, American journal of diseases of children.
[19] N. Blin,et al. A general method for isolation of high molecular weight DNA from eukaryotes. , 1976, Nucleic acids research.
[20] J. Parker,et al. Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia. , 1991, Blood.
[21] O. Platt,et al. Mortality in sickle cell disease. Life expectancy and risk factors for early death. , 1994, The New England journal of medicine.
[22] E. Fabricius,et al. Determination of hydroxyurea in mammalian tissues and blood. , 1971, Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research.
[23] Y. Kan,et al. Detection of sickle cell anaemia and thalassaemias , 1987, Nature.
[24] S. Orkin,et al. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster , 1982, Nature.
[25] E. Baysal,et al. The β- and δ-Thalassemia Repository (Eighth Edition) , 1995 .
[26] W. Schroeder,et al. β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California , 1989 .
[27] M. Steinberg,et al. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. , 1984, Blood.
[28] George J. Dover,et al. Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments] , 1992 .
[29] G. Dover,et al. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age. , 1995, Blood.
[30] W. Feder,et al. Effective Increase in Nematode Populations by the Addition of Aureomycin , 1959, Nature.
[31] L. Benjamin,et al. Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia , 1995, American journal of hematology.
[32] J. Niland,et al. Chronic renal failure in sickle cell disease: risk factors, clinical course, and mortality. , 1991, Annals of internal medicine.
[33] Y. C. Chang,et al. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2 , 1992 .
[34] D. Meyers,et al. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. , 1992, Blood.
[35] D. Labie,et al. Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[36] G. Lathrop,et al. Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers. , 1994, American journal of human genetics.
[37] D. Powars. Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features. , 1991, Hematology/oncology clinics of North America.
[38] H. Origasa. Longitudinal Data Analysis Using Linear Models , 1988 .
[39] G. Dover,et al. Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production. , 1987, Blood.
[40] T. Ley,et al. Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production. , 1986, Blood.
[41] R. J. Hayes,et al. The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations , 1985, British journal of haematology.
[42] G. Dover,et al. Individual variation in the production and survival of F cells in sickle-cell disease. , 1978, The New England journal of medicine.
[43] Richard F. Gunst,et al. Applied Regression Analysis , 1999, Technometrics.
[44] K. Betke,et al. Estimation of Small Percentages of Fœtal Hæmoglobin , 1959, Nature.
[45] J. Smith,et al. Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease. , 1992, Journal of clinical epidemiology.
[46] P. Lauf,et al. Hydroxyurea affects cell morphology, cation transport, and red blood cell adhesion in cultured vascular endothelial cells. , 1994, Blood.
[47] P. Dr,et al. Sickle cell anemia: beta s-gene-cluster haplotypes as prognostic indicators of vital organ failure. , 1991, Seminars in hematology.
[48] F. Barton,et al. Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea. , 1995, Controlled clinical trials.
[49] A. Schechter,et al. Augmentation by erythropoietin of the fetal-hemoglobin response to hydroxyurea in sickle cell disease. , 1993, The New England journal of medicine.