Sickle cell disease.

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[27]  J. Schatz,et al.  Neuropsychologic effects of stroke in children with sickle cell anemia. , 1993, The Journal of pediatrics.

[28]  D. Fairclough,et al.  A randomized study of outpatient treatment with ceftriaxone for selected febrile children with sickle cell disease. , 1993, The New England journal of medicine.

[29]  J. Weil,et al.  Pathogenesis of Lung Disease in Sickle Hemoglobinopathies , 1993 .

[30]  M. Gelfand,et al.  Simultaneous occurrence of rib infarction and pulmonary infiltrates in sickle cell disease patients with acute chest syndrome. , 1993, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[31]  A. Qudah,et al.  Acute splenic sequestration together with aplastic crisis caused by human parvovirus B19 in patients with sickle cell disease. , 1993, The Journal of pediatrics.

[32]  A. Wayne,et al.  Transfusion management of sickle cell disease , 1993 .

[33]  E. Sariban,et al.  Bone marrow transplantation corrects the splenic reticuloendothelial dysfunction in sickle cell anemia. , 1993, Blood.

[34]  M. Espeland,et al.  Developmental Screening in Young Children with Sickle Cell Disease: Results of a Cooperative Study , 1993, The American journal of pediatric hematology/oncology.

[35]  C. McLaren,et al.  Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major , 1993, American journal of hematology.

[36]  S. Miller,et al.  Transient aplastic crisis in patients with sickle cell disease. B19 parvovirus studies during a 7-year period. , 1992, American journal of diseases of children.

[37]  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.

[38]  J. Scott,et al.  Neurologic events after partial exchange transfusion for priapism in sickle cell disease. , 1992, The Journal of pediatrics.

[39]  George J. Dover,et al.  Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments] , 1992 .

[40]  Richard D Moore,et al.  Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia. , 1992, Blood.

[41]  J. Silber,et al.  A modified transfusion program for prevention of stroke in sickle cell disease. , 1992, Blood.

[42]  J. Morris,et al.  Stroke in a cohort of patients with homozygous sickle cell disease. , 1992, The Journal of pediatrics.

[43]  R. Adams,et al.  The use of transcranial ultrasonography to predict stroke in sickle cell disease. , 1992, The New England journal of medicine.

[44]  Scott T. Miller,et al.  Less intensive long-term transfusion therapy for sickle cell anemia and cerebrovascular accident. , 1992, The Journal of pediatrics.

[45]  G. Buchanan,et al.  A fatal case of acute splenic sequestration in a 53-year-old woman with sickle-hemoglobin C disease. , 1992, The American journal of medicine.

[46]  C. Stocking,et al.  Bone marrow transplantation for sickle cell disease. A study of parents' decisions. , 1991, The New England journal of medicine.

[47]  J. Niland,et al.  Chronic renal failure in sickle cell disease: risk factors, clinical course, and mortality. , 1991, Annals of internal medicine.

[48]  E Vichinsky,et al.  Pain in sickle cell disease. Rates and risk factors. , 1991, The New England journal of medicine.

[49]  E. Vichinsky.  Comprehensive care in sickle cell disease: its impact on morbidity and mortality. , 1991, Seminars in hematology.

[50]  K. Ohene‐Frempong.  Stroke in sickle cell disease: demographic, clinical, and therapeutic considerations. , 1991, Seminars in hematology.

[51]  Cage S. Johnson,et al.  Vascular occlusion in sickle cell disease: current concepts and unanswered questions. , 1991, Blood.

[52]  R. Mulhern,et al.  High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease. , 1991, The Journal of pediatrics.

[53]  R. Hebbel.  Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology. , 1991, Blood.

[54]  K. Chirgwin,et al.  Role of Chlamydia pneumoniae in acute chest syndrome of sickle cell disease. , 1991, The Journal of pediatrics.

[55]  G. Buchanan,et al.  Outpatient management of febrile illness in infants and young chlidren with sickle cell anemia , 1990 .

[56]  O. Castro,et al.  Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease , 1990 .

[57]  R. Ware,et al.  Long-term management of splenic sequestration in children with sickle cell disease. , 1990, The Journal of pediatrics.

[58]  R. A. Johnson,et al.  Alloimmunization in sickle cell anemia and transfusion of racially unmatched blood. , 1990, The New England journal of medicine.

[59]  S. Piomelli,et al.  Planning an exchange transfusion in patients with sickle cell syndromes. , 1990, The American journal of pediatric hematology/oncology.

[60]  V. Mckie,et al.  Splenic phagocytic function in children with sickle cell anemia receiving long-term hypertransfusion therapy. , 1989, The Journal of pediatrics.

[61]  S. Leikin,et al.  Mortality in children and adolescents with sickle cell disease. Cooperative Study of Sickle Cell Disease. , 1989, Pediatrics.

[62]  A. Pappo,et al.  Acute splenic sequestration in a 2-month-old infant with sickle cell anemia. , 1989, Pediatrics.

[63]  M. Gaston,et al.  Newborn screening for sickle cell disease and other hemoglobinopathies. , 1989, Pediatrics.

[64]  T. Savitt,et al.  Herrick's 1910 case report of sickle cell anemia. The rest of the story. , 1989, JAMA.

[65]  A. Mallouh,et al.  Beneficial effect of blood transfusion in children with sickle cell chest syndrome. , 1988, American journal of diseases of children.

[66]  A. Schechter,et al.  Levels of fetal hemoglobin necessary for treatment of sickle cell disease. , 1988, The New England journal of medicine.

[67]  T. Hays,et al.  Experience with donors matched for minor blood group antigens in patients with sickle cell anemia who are receiving chronic transfusion therapy , 1987, Transfusion.

[68]  R. Grover,et al.  Reversibility of splenic function by transfusion in two young adults with sickle cell anemia. , 1987, The American journal of pediatric hematology/oncology.

[69]  G. Buchanan,et al.  Intravenous narcotic therapy for children with severe sickle cell pain crisis. , 1986, American journal of diseases of children.

[70]  J. Verter,et al.  Bacteremia in sickle hemoglobinopathies. , 1986, The Journal of pediatrics.

[71]  G. Maude,et al.  Clinical presentation of sickle cell-hemoglobin C disease. , 1986, The Journal of pediatrics.

[72]  E Vichinsky,et al.  Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial. , 1986, The New England journal of medicine.

[73]  R. Allison,et al.  Pulmonary edema. Complication in the management of sickle cell pain crisis. , 1986, The American journal of medicine.

[74]  G. Buchanan,et al.  Acute chest syndrome in children with sickle cell disease. A retrospective analysis of 100 hospitalized cases. , 1986, The American journal of pediatric hematology/oncology.

[75]  M. Poncz,et al.  Acute chest syndrome in sickle cell disease: etiology and clinical correlates. , 1985, The Journal of pediatrics.

[76]  M. Espeland,et al.  Developmental pattern of splenic dysfunction in sickle cell disorders. , 1985, Pediatrics.

[77]  D. Higgs,et al.  Acute splenic sequestration in homozygous sickle cell disease: natural history and management. , 1985, The Journal of pediatrics.

[78]  D. Higgs,et al.  Clinical presentation of homozygous sickle cell disease. , 1985, The Journal of pediatrics.

[79]  M. Stevens,et al.  Haematological change in sickle cell–haemoglobin C disease and in sickle cell‐beta thalassaemia: a cohort study from birth , 1985, British journal of haematology.

[80]  O. Platt,et al.  Influence of sickle hemoglobinopathies on growth and development. , 1984, The New England journal of medicine.

[81]  M. Reivich,et al.  Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease. , 1984, Blood.

[82]  E. Orringer,et al.  Pulmonary hypertension and cor pulmonale in the sickle hemoglobinopathies. , 1982, The American journal of medicine.

[83]  G. Serjeant,et al.  Causes of death in sickle-cell disease in Jamaica. , 1982, British medical journal.

[84]  G. Buchanan,et al.  Acute infarction of long bones in children with sickle cell anemia. , 1982, The Journal of pediatrics.

[85]  M. Stevens,et al.  Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. , 1981, Archives of disease in childhood.

[86]  G. Serjeant,et al.  Observations on the Natural History of Dactylitis in Homozygous Sickle Cell Disease , 1981, Clinical pediatrics.

[87]  M. Stevens,et al.  Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. , 1981, The Journal of pediatrics.

[88]  T. Slovis,et al.  Incidence of cholelithiasis in sickle cell anemia using the ultrasonic gray-scale technique. , 1980, The Journal of pediatrics.

[89]  J. Langston,et al.  Efficacy of transfusion therapy for one to two years in patients with sickle cell disease and cerebrovascular accidents. , 1980, The Journal of pediatrics.

[90]  D. Solanki,et al.  Severe mycoplasma pneumonia with pleural effusions in a patient with sickle cell-hemoglobin C(SC) disease. Case report and review of the literature. , 1979, The American journal of medicine.

[91]  J. Lobel,et al.  Developmental aspects of splenic function in sickle cell diseases. , 1979, Blood.

[92]  C. Pegelow,et al.  The natural history of stroke in sickle cell disease. , 1978, The American journal of medicine.

[93]  G. Serjeant,et al.  Early deaths in Jamaican children with sickle cell disease. , 1978, British medical journal.

[94]  D. Powars.  Natural history of sickle cell disease--the first ten years. , 1975, Seminars in hematology.

[95]  E. Barrett-Connor.  Pneumonia and pulmonary infarction in sickle cell anemia. , 1973, JAMA.

[96]  S. Levinson,et al.  CLINICAL LABORATORY DIAGNOSIS , 1937 .