« Previous
Next »
Blood Reviews
Volume 19, Issue 2
, Pages 99-110
, March 2005
Three decades of innovation in the management of sickle cell disease: the road to understanding the sickle cell disease clinical phenotype
References
-
Gaston MH, Rosse WF and the Cooperative Group. The cooperative study of sickle cell disease: review of study design and objectives. Am J Pediatr Hematol/Oncol 1982;4:197–201
-
Gaston M, Smith J, Gallagher D, Flournoy-Gill Z, West S, Bellevue R, et al. and the CSSCD Study Group. Recruitment in the cooperative study of sickle cell disease (CSSCD). Contr Clin Trials 1987;8:131S–40S
-
Gaston MH, Verter JI, Woods G, Pegelow C, Kelleher J, Presbury G, et al. and the Prophylactic Penicillin Study Group. Prophylaxis with oral penicillin in children with sickle cell anemia. New Engl J Med 1986;314:1593–99
- . Sickle cell anaemia trial. Stat. Med. 1990;9:45–51
-
Pain in sickle cell disease: rates and risk factors.
New Engl. J. Med. 1991;325:11–16
-
Farber MD, Koshy M, Kinney TR and the Cooperative Group. Cooperative study of sickle cell disease: demographic and socioeconomic characteristics of patients and families with sickle cell disease. J Chron Dis 1985;38:495–505
-
West MS, Wethers D, Smith J, Steinberg M. and the Cooperative Study of Sickle Cell Disease. Laboratory profile of sickle cell disease: a cross-sectional analysis. J Clin Epidemiol 1992;45:893–909
-
.
Reference values and hematologic changes from birth to five years in patients with sickle cell disease.
Arch. Pediatr. Adolescent Med. 1994;148:1156–1162
-
Pearson HA, Gallagher MS, Chilcote R, Sullivan E, Wilmas J, Espeland M, et al. and the Cooperative Group. Developmental pattern of splenic dysfunction in sickle cell disorders. Pediatrics 1985;76:392–97
- Leg ulcers in patients with sickle cell disease. Blood. 1989;74:1403–1408
-
Sickle cell disease as a cause of osteonecrosis of the femoral head.
New Engl. J. Med. 1991;325:1476–1481
-
Osteonecrosis of the humeral head in sickle cell disease.
Orthop. Rel. Res. 1993;289:136–143
- . Developmental screening in young children with sickle cell disease: results of a cooperative study. Am. J. Pediatr. Hematol. Oncol. 1993;15:87–91
- Cognitive functioning and brain magnetic resonance imaging in children with sickle cell disease. Pediatrics. 1996;97:864–870
-
The spectrum of brain MR abnormalities in sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease.
Am. J. Neuroradiol. 1996;17:965–972
- Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998;91:288–294
- Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. Pediatrics. 1999;103:640–645
- The acute chest syndrome in sickle cell disease: incidence and risk factors. Blood. 1994;84:643–649
- . Acute chest syndrome in sickle cell disease: clinical presentation and course. Blood. 1997;89:1787–1792
- . The heart in sickle cell anemia: the cooperative study of sickle cell disease (CSSCD). Chest. 1995;108:1214–1219
-
Rosse WF, Gallagher D, Kinney TR, Castro O, Dosik H, Moohr J, et al. and the CSSCD. Transfusion and alloimmunization in sickle cell disease. Blood 1990;76:1431–7
-
.
Influence of sickle hemoglobinopathies on growth and development.
New Engl. J. Med. 1984;311:7–12
- . Reliability of Tanner stage assessments in a multi-center study. Am. J. Hum. Biol. 1990;2:503–510
-
Zarkowsky HS, Gallagher D, Gill FM, Wang W, Falletta JM, Lande WM, et al. and the Cooperative Group. Bacteremia in sickle hemoglobinopathies. J Pediatr 1986;109:579–85
-
Newborn experience in the cooperative study of sickle cell disease.
Pediatr. Suppl. 1989;83:827–829
- Clinical events in the first decade in a cohort of infants with sickle cell disease. Blood. 1995;86:776–783
-
.
The influence of infant and maternal sickle cell disease on birth outcome and neonatal course.
Arch. Pediatr. Adolescent Med. 1994;148:1156–1162
-
Leikin SL, Gallagher D, Kinney TR, Sloane D, Klug P, Rida W and the CSSCD. Mortality in children and adolescents with sickle cell disease. Pediatrics 1989;84:500–8
-
Prediction of adverse outcomes in children with sickle cell disease.
New Engl. J. Med. 2000;342:83–89
- Surgery and anesthesia in sickle cell disease. Blood. 1995;86:3676–3684
- . Pregnancy in sickle cell disease: experience of the cooperative study of sickle cell disease. Obstet. Gynecol. 1996;87:199–204
- Natural history of blood pressure in sickle cell disease: risks for stroke and death associated with relative hypertension in sickle cell anemia. Am. J. Med. 1997;102:171–177
-
Mortality in sickle cell disease: life expectancy and risk factors for early death.
New Engl. J. Med. 1994;330:1639–1644
-
Steinberg MH, Rosenstock W, Coleman MB, Adams JG, Platica O, Cedeno M, et al. and the Cooperative Group. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia. Blood 1984;63:1353–60
-
Embury SH, Gholson MA, Gillette P, Rieder RF. and the Cooperative Group. The leftward deletion [α-THAL-2] á-Thal-2 haplotype in a black subject with hemoglobin SS. Blood 1985;65:769–71
- . Estimation of growth curves from longitudinal data collected at irregular time intervals. Comput. Biomed. Res. 1986;19:575–587
-
Steinberg MH, West MS, Gallagher D, Mentzer W and the CSSCD. Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell disease. Blood 1988;71:748–52
-
.
Joint estimation of incidence and diagnostic error rates from irregular longitudinal data.
J. Am. Stat. Assoc. 1989;84:972–979
- . Estimating incidence and diagnostic error rates for bivariate progressive processes. Biometrics. 1993;49:1010–1021
-
Causes and outcomes of the acute chest syndrome in sickle cell disease.
New Engl. J. Med. 2000;342:1855–1865
- Discontinuing penicillin prophylaxis in children with sickle cell anemia. J. Pediatr. 1995;127:685–690
- Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia. Blood. 1992;79:2555–2565
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia.
New Engl. J. Med. 1995;332:1317–1322
- Hydroxyurea and sickle cell anemia: clinical utility of a myelosuppressive “switching” agent. Medicine. 1996;75:300–325
- . Fetal hemoglobin in sickle cell anemia: relation to regulatory sequences cis to the Beta-globin gene. Blood. 1996;87:1604–1611
-
Effects of hydroxyurea administration on the body-weight, body composition, and exercise performance of patients with sickle cell anaemia.
Clin. Sci. 1997;92:481–486
-
Moore RD, Charache S, Terrin ML, Barton FB, Ballas SK and the Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. Cost-effectiveness of hydroxyurea in sickle cell anemia. Am J Hematol 2000;64:26–31
-
A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease.
New Engl. J. Med. 1995;333:206–213
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial doppler ultrasonography.
New Engl. J. Med. 1998;339:5–11
- Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS Study, a phase I/II trial. Blood. 1999;94:1550–1554
-
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia; risks and benefits up to9 years of treatment.
J. Am. Med. Assoc. 2003;289:1645–1651
PII: S0268-960X(04)00020-7
doi: 10.1016/j.blre.2004.04.002
« Previous
Next »
Blood Reviews
Volume 19, Issue 2
, Pages 99-110
, March 2005
