C. Johnson

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The sickle cell hemolytic transfusion reaction syndrome

Cage S. Johnson, I. Shulman, L. Petz, 1997, Transfusion.

On the birth of an infant with sickle cell anemia.

C. Pegelow, W. Schroeder, D. Powars, 1977, Hemoglobin.

Vascular occlusion in sickle cell disease: current concepts and unanswered questions.

Cage S. Johnson, R. Francis, C. Johnson, 1991, Blood.

Arterial blood pressure in adults with sickle cell disease.

C. Johnson, A. J. Giorgio, 1981, Archives of internal medicine.

Myocardial infarction in sickle cell disease.

L. Haywood, D. Tatter, C. Cobb, 1996, Journal of the National Medical Association.

Glycosylated minor C, D, and E hemoglobins.

E. Beutler, S. Rahbar, K. Blume, 1981, Biochemical medicine.

Pernicious anemia in Latin Americans is not a disease of the elderly.

J. Weiner, R. Carmel, C. Johnson, 1987, Archives of internal medicine.

Unsuspected pernicious anemia in a patient with sickle cell disease receiving routine folate supplementation.

R. Carmel, M. Siegel, R. Sinow, 1987, Archives of internal medicine.

Racial patterns in pernicious anemia. Early age at onset and increased frequency of intrinsic-factor antibody in black women.

R. Carmel, C. Johnson, 1978, The New England journal of medicine.

Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity.

H. Meiselman, Cage S. Johnson, D. Powars, 1994, The American journal of pediatric hematology/oncology.

Iron deficiency occurs frequently in patients with pernicious anemia.

J. Weiner, R. Carmel, C. Johnson, 1987, JAMA.

Liver Involvement in Sickle Cell Disease

M. Omata, J. Weiner, M. Tong, 1985, Medicine.

Platelet-activating factor in plasma of patients with sickle cell disease in steady state.

J. Raj, B. Ibe, J. Kurantsin-Mills, 1997, The Journal of laboratory and clinical medicine.

Blood transfusions and immunophenotypic alterations of lymphocyte subsets in sickle cell anemia. The Transfusion Safety Study Group.

C. Pegelow, E. Operskalski, M. Hilgartner, 1995, Blood.

Sickle cell anemia: does myocardial ischemia occur during crisis?

L. Haywood, S. Norris, C. Johnson, 1991, Journal of the National Medical Association.

Acute myocardial infarction in sickle cell anemia.

L. Haywood, D. Tatter, C. Cobb, 1983, Archives of internal medicine.

6 Rheology of the sickle cell disorders

J. Stuart, C. Johnson, 1987 .

Failure of methylene blue treatment in toxic methemoglobinemia. Association with glucose-6-phosphate dehydrogenase deficiency.

E. Beutler, P. Rosen, W. McGehee, 1971, Annals of internal medicine.

alpha-Thalassemia: prevalence and hematologic findings in American Blacks.

E. Beutler, C. Johnson, C. Tegos, 1982, Archives of internal medicine.

Mechanical properties of oxygenated red blood cells in sickle cell (HbSS) disease.

H J Meiselman, H. Meiselman, G. Nash, 1984, Blood.

Human red cells protein kinase in normal subjects and patients with hereditary spherocytosis, sickle cell disease, and autoimmune hemolytic anemia.

E. Guinto, C. Johnson, E. Beutler, 1976, Blood.

Effect of polymerization tendency on haematological, rheological and clinical parameters in sickle cell anaemia

A. Girling, J. Stuart, C. Noguchi, 1989, British journal of haematology.

Chronic renal failure in sickle cell disease: risk factors, clinical course, and mortality.

J. Niland, Cage S. Johnson, L. Opas, 1991, Annals of internal medicine.

The effect of fetal hemoglobin on the sickling dynamics of SS erythrocytes.

H. Meiselman, C. Johnson, L. Sewchand, 1983, Blood cells.

Pharmacological modification of oxygen affinity improves deformability of deoxygenated sickle erythrocytes: a possible therapeutic approach to sickle cell disease.

J. Stuart, M. Sowter, C. Johnson, 1989, Clinical science.

Modification of Oxygen Affinity in Sickle Cell Anemia

J. Stuart, R. D. White, M. Sowter, 1989 .

Erythrocyte pyridoxine kinase levels in patients with sideroblastic anemia.

R. Chillar, C. Johnson, E. Beutler, 1976, The New England journal of medicine.

Multisystem damage associated with tricorporal priapism in sickle cell disease.

D. Powars, Z. Rogers, C. Johnson, 1993, The American journal of medicine.

Electrocardiogram analysis in adult patients with sickle cell disease.

L. Haywood, C. Johnson, K. Holloman, 1987, Journal of the National Medical Association.

Pregelation aggregation of sickle cell hemoglobin.

J. T. Penniston, M. Luzzana, C. Johnson, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Influence of oxygen tension on the viscoelastic behavior of red blood cells in sickle cell disease.

H J Meiselman, H. Meiselman, G. Nash, 1986, Blood.

Prevalence of glucose-6-phosphate dehydrogenase deficiency in sickle-cell disease.

E. Beutler, D. Powars, C. West, 1974, The New England journal of medicine.

Serum Autoantibodies in Patients With Sickle Cell Anemia

F. Quismorio, C. Johnson, 1984, The American journal of the medical sciences.

Iron-deficiency anemia: a medically treatable chronic anemia as a model for transfusion overuse.

A. Rabinowitz, I. Shulman, S. Saxena, 1993, The American journal of medicine.

Transient stress lymphocytosis during crisis of sickle cell anemia and emergency trauma and medical conditions. An immunophenotyping study.

R. Brynes, J. Parker, D. Endres, 1990, Archives of Pathology & Laboratory Medicine.

Rheology of the sickle cell disorders.

J. Stuart, C. Johnson, 1987, Bailliere's clinical haematology.

Thalassemia minor: routine erythrocyte measurements and differentiation from iron deficiency.

E. Beutler, C. Johnson, C. Tegos, 1983, American journal of clinical pathology.

Profiles of black and Latin-American patients having pernicious anemia. HLA antigens, lymphocytotoxic antibody, anti-parietal cell antibody serum gastrin levels, and ABO blood groups.

K. Tung, P. Terasaki, R. Carmel, 1981, American journal of clinical pathology.

Rheologic impairment of sickle RBCs induced by repetitive cycles of deoxygenation-reoxygenation.

H. Meiselman, G. Nash, C. Johnson, 1988, Blood.

Masking of macrocytosis by alpha-thalassemia in blacks with pernicious anemia.

E. Beutler, R. Carmel, W. Kuhl, 1982, The New England journal of medicine.

alpha-Thalassemia: prevalence and hematologic findings in American Blacks.

E. Beutler, C. Johnson, C. Tegos, 1982, Archives of Internal Medicine.

Intravenous iron-dextran in the treatment of iron deficient anemia.

C. Johnson, 1979, Journal of the National Medical Association.

Left ventricular filling pressure in sickle cell anemia.

L. Haywood, S. Norris, C. Johnson, 1992, Journal of the Association for Academic Minority Physicians : the official publication of the Association for Academic Minority Physicians.

The first example of a deletion in the human alpha chain: hemoglobin Boyle Heights or alpha 2 6 (A4) Asp----to O beta 2.

W. Schroeder, J. Shelton, J. B. Shelton, 1983, Hemoglobin.