S. Charache

R. Adams, S. Charache, S. Sarnaik, 1990, Journal of the Association for Academic Minority Physicians : the official publication of the Association for Academic Minority Physicians.

Delta-beta-thalassemia is due to a gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.

S. Antonarakis, A. F. Scott, S. Charache, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Iron deficiency anemia: mitochondrial alpha-glycerophosphate dehydrogenase in guinea pig skeletal muscle.

S. Charache, V. Macdonald, P. Hathaway, 1985, The Journal of laboratory and clinical medicine.

5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimens.

G. Dover, S. Boyer, S. Charache, 1985, Blood.

Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore.

D. Weatherall, S. Charache, M. Shepard, 1963, Blood.

Instant blood counts.

S. Charache, 1985, Annals of internal medicine.

Eye disease in sickling disorders.

S. Charache, 1996, Hematology/oncology clinics of North America.

Familial erythrocytosis due to electrophoretically undetectable hemoglobin with impaired oxygen dissociation (hemoglobin Malmö, alpha 2 beta 2 97 gln).

S. Boyer, S. Charache, V. Fairbanks, 1971, Mayo Clinic proceedings.

Electronic blood cell counters. Faulty calibration due to type and amount of anticoagulant in collection tubes.

S. Charache, M. Perlstein, D. Sears, 1985, Archives of pathology & laboratory medicine.

Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate

S. Brusilow, G. Dover, S. Charache, 1994 .

Pharmacological modification of hemoglobin F expression in sickle cell anemia: An update on hydroxyurea studies

S. Charache, 1993, Experientia.

Sickle-Cell Anemia: The Known and the Unknown

S. Charache, 1972 .

Cost‐effectiveness of hydroxyurea in sickle cell anemia

Richard D Moore, F. Barton, S. Charache, 2000, American journal of hematology.

Problems in transfusion therapy.

S. Charache, 1990, New England Journal of Medicine.

Transfusion of racially unmatched blood.

R. A. Johnson, E. Vichinsky, S. Charache, 1990, The New England journal of medicine.

5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimens

G. Dover, S. Boyer, S. Charache, 1985 .

Progress toward Increasing Fetal Hemoglobin Production in Man: Experience with 5‐Azacytidine and Hydroxyurea a

G. Dover, S. Boyer, S. Charache, 1985, Annals of the New York Academy of Sciences.

Oxygen equilibrium of hemoglobin J Cape Town.

S. Charache, T. Jenkins, 1971, The Journal of clinical investigation.

Evaluation of extracorporeal alkylation of red cells as a potential treatment for sickle cell anemia.

R. Dreyer, S. Charache, C. Hsu, 1976, Blood.

Infarction of bone marrow in the sickle cell disorders.

D. Page, S. Charache, 1967, Annals of internal medicine.

LIGAND BINDING TO HEMOGLOBINS: EFFECTS OF GLOBIN STRUCTURE

W. Caughey, S. Charache, A. Lanir, 1978 .

Properties of hemoglobin a and hemoglobin Zurich (β63 histidine→arginine): Quantitative evaluation of functional abnormalities in hemoglobins

J. A. Volpe, W. Caughey, S. Charache, 1976 .

Oxidation of Carbonyl

W. Caughey, S. Charache, A. Lanir, 2005 .

Variability of oxygen affinity of blood: human subjects native to high altitude.

R. Winslow, S. Charache, R. Berger, 1981, Journal of applied physiology: respiratory, environmental and exercise physiology.

5-Azacytidine acts directly on both erythroid precursors and progenitors to increase production of fetal hemoglobin.

T. Ley, A. Nienhuis, R. Humphries, 1985, The Journal of clinical investigation.

Pregnancy in carriers of high-affinity hemoglobins.

R. Williams, P. Catalano, S. Charache, 1985, Blood.

Treatment of sickle cell anemia with hydroxyurea and erythropoietin.

M. Goldberg, C. Brugnara, L. Schapira, 1990, The New England journal of medicine.

Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell disease.

G. Dover, S. Charache, 1992, Seminars in oncology.

Hydroxyurea as treatment for sickle cell anemia.

S. Charache, 1991, Hematology/oncology clinics of North America.

Hydroxyurea induction of hemoglobin F production in sickle cell disease: relationship between cytotoxicity and F cell production.

T. Ley, A. Nienhuis, R. Humphries, 1986, Blood.

Postsynthetic deamidation of hemoglobin Providence (beta 82 Lys replaced by Asn, Asp) and its effect on oxygen transport.

R. Winslow, R. V. Van Beneden, S. Charache, 1977, The Journal of clinical investigation.

Polycythemia produced by hemoglobin Osler (beta-145 (HC2) Tyr yields Asp).

S. Charache, R. Jones, B. Brimhall, 1975, The Johns Hopkins medical journal.

Comparison of the effects of lower monohydric alcohols and inositol hexaphosphate on the oxidation of hemoglobin by menadione.

S. Charache, V. Macdonald, 1982, Biochimica et biophysica acta.

Nuclear magnetic resonance studies of hemoglobin. IV. The structure-function relationship of human adult hemoglobins A and Chesapeake and its implication to the nature of oxygenation of hemoglobin.

D. G. Davis, C. Ho, S. Charache, 1970, Biochemical and biophysical research communications.

Hydroxyurea and Sickle Cell Anemia Clinical Utility of a Myelosuppressive “Switching” Agent

M L Terrin, F. Barton, O. Castro, 1996, Medicine.

PROLONGED SURVIVAL OF A PATIENT WITH SICKLE CELL ANEMIA.

S. Charache, S. Richardson, 1964, Archives of internal medicine.

The Effect of Hemoglobin F-Chesapeake (α292 Arg. → Leuγ2) on Fetal Oxygen Affinity and Erythropoiesis

S. Charache, P. Hathaway, Clyde Jones, 1979, Pediatric Research.

RATE OF SICKLING OF RED CELLS DURING DEOXYGENATION OF BLOOD FROM PERSONS WITH VARIOUS SICKLING DISORDERS.

S. Charache, C. Conley, 1964, Blood.

Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea.

F. Barton, S. Eckert, G. Dover, 1995, Controlled clinical trials.

Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.

G. Dover, S. Boyer, S. Charache, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivo

G. Dover, S. Charache, S. Ballas, 1989, American journal of hematology.

The Negro Variety of Hereditary Persistence of Fetal Haemoglobin is a Mild Form of Thalassaemia

J. Clegg, D. Weatherall, S. Charache, 1976, British journal of haematology.

Nuclear magnetic resonance studies of hemoglobin Chesapeake: an alpha1beta2 mutant.

C. Ho, S. Charache, K. Wiechelman, 1974, Biochemistry.

Nuclear magnetic resonance studies of hemoglobins. VI. Heme proton spectra of human deoxyhemoglobins and their relevance to the nature of co-operative oxygenation of hemoglobin.

D. G. Davis, C. Ho, J. Baldassare, 1971, Journal of molecular biology.

Electron paramagnetic resonance studies of spin-labeled hemoglobins. II. Roles of subunit interactions and of intermediate structures in the cooperative oxygenation of hemoglobin and the results of hemoglobin Yakima, hemoglobin J capetown, and carboxypeptidases A and B treated hemoglobin A.

C. Ho, J. Baldassare, S. Charache, 1970, Biochemistry.

Studies on the folic acid vitamins. V. The effect of folic acid on the citrovorum factor activity of mouse liver

A. Goldin, S. Charache, S. R. Humphreys, 1960, Cancer.

Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea.

M L Terrin, F. Barton, M. Steinberg, 1997, Blood.

Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments]

George J. Dover, Richard D. Moore, Richard D Moore, 1992 .

Chemotherapy and Hemoglobin F Synthesis in Sickle Cell Disease a

G. Dover, S. Charache, 1989, Annals of the New York Academy of Sciences.

Treatment of sickle cell anemia.

S. Charache, 1981, Annual review of medicine.

Deletion of the β-globin structure gene in hereditary persistence of foetal haemoglobin

S. Charache, H. Kazazian, A. Dozy, 1975, Nature.

Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia.

Richard D Moore, O. Platt, E. Orringer, 1992, Blood.

Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia.

G. Dover, S. Charache, G J Dover, 1987, Blood.

Hemoglobin aggregation and pseudosickling in vitro of hemoglobin setif‐containing erythrocytes

C. Noguchi, S. Charache, J. Blanchette-Mackie, 1991, American journal of hematology/oncology.

Increasing fetal hemoglobin production in sickle cell disease: results of clinical trials.

G. Dover, S. Charache, 1987, Progress in clinical and biological research.

Fetal hemoglobin, sickling, and sickle cell disease.

S. Charache, Samuel Charache, 1990, Advances in pediatrics.

5-Azacytidine increases fetal hemoglobin production in a patient with sickle cell disease.

G. Dover, S. Boyer, S. Charache, 1983, Progress in clinical and biological research.

Effects of blood transfusion on exercise capacity in patients with sickle-cell anemia.

E. Bleecker, S. Charache, D. Bross, 1983, The American journal of medicine.

Stimulation of fetal hemoglobin production by hydroxyurea in sickle cell anemia.

G. Dover, S. Charache, 1989, Progress in clinical and biological research.

Failure of desmopressin to lower serum sodium or prevent crisis in patients with sickle cell anemia

S. Charache, W. Walker, 1981 .

Hereditary persistence of fetal hemoglobin. Heterogeneity of fetal hemoglobin in homozygotes and in conjunction with -thalassemia.

G. Apell, T. Huisman, S. Charache, 1971, The New England journal of medicine.

Hemoglobin Hasharon (α247 his(CD5)β2): a hemoglobin found in low concentration

S. Charache, U. Gessner, A. Mondzac, 1969 .

Postsynthetic Deamidation of Hemoglobin Providence (, 82 Lys > Asn, Asp) and its Effect on Oxygen Transport

S. Charache, M. Jessop, R. V. Beneden, 2022 .

HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN 1

S. Charache, C. Conley, Samuel Charache, 1969, Annals of the New York Academy of Sciences.

Pseudosickling of hemoglobin Setif

S. Charache, P. Fleming, E. Powell, 1987 .

Effect of 2,3-diphosphoglycerate on oxygen affinity of blood in sickle cell anemia.

S. Grisolía, S. Charache, A. Hellegers, 1970, The Journal of clinical investigation.

Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease.

S. Charache, D. F. Waugh, S Charache, 1967, The Journal of clinical investigation.

THALASSEMIA IN BLACK AMERICANS *

S. Charache, C. Conley, M. Bartalos, 1974, Annals of the New York Academy of Sciences.

Ophthalmologic manifestations of sickle cell thalassemia.

S. Charache, M. Goldberg, M. Goldberg, 1971, Archives of internal medicine.

Pregnancy in sickle cell disease.

S. Charache, J. Niebyl, 1985, Clinics in haematology.

Management of Sickle Cell Disease in Pregnant Patients

S. Charache, D. Bonds, J. Niebyl, 1980, Obstetrics and gynecology.

Pseudosickling of hemoglobin Setif.

S. Charache, P. Fleming, E. Powell, 1987, Blood.

Hb Potomac (101 Glu replaced by Asp): speculations on placental oxygen transport in carriers of high-affinity hemoglobins.

R. Winslow, S. Charache, R. Jones, 1978, Blood.

Methods for Measurement of Oxygen Affinity

S. Charache, 1974 .

a Hemoglobin Found in Low Concentration

S. Charache, A. Mondzac, E. E. Gayle, 1969 .

Life span of carbamylated red cells in sickle cell anemia.

S. Charache, P. Milner, 1973, Journal of Clinical Investigation.

Polycythemia associated with a hemoglobinopathy.

J. Clegg, D. Weatherall, S. Charache, 1966, The Journal of clinical investigation.

5 Haemochromatosis and diabetes

C. Saudek, S. Charache, 1992 .

Failure of desmopressin to lower serum sodium or prevent crisis in patients with sickle cell anemia.

S. Charache, W. Walker, 1981, Blood.

Toxic-therapeutic ratio of sodium cyanate.

S. Charache, N. Jander, T. Duffy, 1975, Archives of internal medicine.

Hemoglobin SC, SS/GPhiladelphia and SOArab diseases diagnostic importance of an integrative analysis of clinical, hematologic and electrophoretic findings.

G. Dover, W. Zinkham, S. Charache, 1977, The American journal of medicine.

Homeostatic responses to increased oxygen affinity.

S. Charache, 1977, Advances in experimental medicine and biology.

Flow cytometric reticulocyte counting with thioflavin T in a clinical hematology laboratory.

S. Charache, D. Metzger, Metzger Dk, 1987, Archives of pathology & laboratory medicine.

A MANIFESTATION OF ABNORMAL HEMOGLOBINS OF MAN: ALTERED OXYGEN AFFINITY * :

S. Charache, 1974, Annals of the New York Academy of Sciences.

Fast hemoglobin in lead poisoning.

D. Weatherall, S. Charache, 1966, Blood.

Binding of 2,3‐diphosphoglycerate to normal and abnormal oxyhemoglobin

S. Grisolía, S. Charache, A. Diederich, 1970, FEBS letters.

Hemoglobin Malmö β-97 (FG-4) Histidine→Glutamine: A Cause of Polycythemia

S. Boyer, S. Charache, V. Fairbanks, 1972 .

Binding of 2,3-Diphosphoglycerate (DPG) to Oxyhemoglobin; Levels and Effect of DPG on Oxygen Affinity of Normal and Abnormal Blood

S. Grisolía, S. Charache, D. Diederich, 1970 .

The molecular basis of hemoglobin Grady.

A. F. Scott, J. Clegg, H. Kazazian, 1981, American journal of human genetics.

A clinical trial of three-part electronic differential white blood cell counts.

S. Charache, P. Metzger, E. Keyser, 1985, Archives of internal medicine.

The organization of hemoglobin in erythrocytes containing hemoglobin A or hemoglobin C.

R. Rand, S. Charache, 1970, Canadian journal of physiology and pharmacology.

Variability of the homeostatic response to altered p50.

R. Winslow, S. Charache, P. Chervenick, 1978, Blood.

Sickle cell anemia.

S. Charache, 1997, Annals of Internal Medicine.

Differences in the reaction sequences associated with drug-induced oxidation of hemoglobins E, S, A, and F.

S. Charache, V. Macdonald, 1983, The Journal of laboratory and clinical medicine.

Abdominal pain in sickle cell disease: the role of CT.

E. Fishman, D. Magid, S. Siegelman, 1987, Radiology.

Experimental therapy of sickle cell disease. Use of hydroxyurea.

S. Charache, 1994, The American journal of pediatric hematology/oncology.

Aplastic crisis due to extensive bone marrow necrosis in sickle cell disease.

D. Pardoll, R. Rodeheffer, S. Charache, 1982, Archives of internal medicine.

Differences in the infrared stretching frequency of carbon monoxide bound to abnormal hemoglobins.

S. Boyer, S. Charache, J. O. Alben, 1969, Biochemistry.

Preoperative transfusion in sickle cell anemia

S. Charache, 1991, American journal of hematology.

Letter: Toxicity of sodium cyanate.

S. Charache, 1974, The New England journal of medicine.

Social disability and psychiatric morbidity in sickle cell anemia and diabetes patients.

M. Folstein, S. Charache, N. Damlouji, 1982, Psychosomatics.

Hematologic changes during sexual maturation. Why do black adolescents have low hemoglobin concentrations?

S. Charache, A. Joffe, H. Wong, 1987, Journal of adolescent health care : official publication of the Society for Adolescent Medicine.

Hemoglobin Hasharon (alpha-2-47 his(CD5)beta-2): a hemoglobin found in low concentration.

S. Charache, U. Gessner, A. Mondzac, 1969, The Journal of clinical investigation.

Nuclear magnetic resonance studies of hemoglobins. VII. Tertiary structure around ligand binding site in carbonmonoxyhemoglobin.

C. Ho, S. Charache, T. Lindstrom, 1972, Biochemistry.

Laboratory evaluation of the Coulter "three-part electronic differential".

S. Charache, P. Metzger, E. Keyser, 1985, American journal of clinical pathology.

Treatment of sickling disorders

S. Charache, 1996, Current opinion in hematology.

Methemoglobinemia--sleuthing for a new cause.

S. Charache, 1986, The New England journal of medicine.

Effect of plasma from patients with liver disease on resistance of red blood cells to lysis by saponin.

S. Charache, S. Margolis, 1969, Journal of Laboratory and Clinical Medicine.

Oxygen equilibrium of hemoglobin J Cape Town.

S. Charache, T. Jenkins, 1971, The Journal of clinical investigation.

Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore.

D. Weatherall, S. Charache, M. Shepard, 1963, Blood.

Studies on the folic acid vitamins. IV. The persistence of amethopterin in mammalian tissues

S. Charache, S. R. Humphreys, P. Condit, 1960, Cancer.

Quality of Life

S. Charache, 2013, Revista brasileira de hematologia e hemoterapia.

MAJOR SITES FOR THE OXYGEN-LINKED BINDING OF CHLORIDE TO HEMOGLOBIN

S. Charache, J. O. Alben, J. Manning, 1978 .

Nuclear magnetic resonance studies of hemoglobiss. V. The heme proton spectra of human deoxyhemoglobins A, F, Zurich, and Chesapeake.

D. G. Davis, C. Ho, S. Charache, 1970, Biochemical and biophysical research communications.

Subunit dissociation of the abnormal hemoglobins G Georgia ( 2 95Leu (G2) 2 ) and Rampa ( 2 95Ser (G2) 2 ).

L. Smith, T. Huisman, S. Charache, 1972, The Journal of biological chemistry.

Hemoglobin Malmö Beta-97 (FG-4) histidine--glutamine: a cause of polycythemia.

S. Boyer, S. Charache, V. Fairbanks, 1972, The Journal of clinical investigation.

Treatment of acute sickle cell crises with a vasopressin analogue

S. Charache, W. Walker, Martha A. Moyer, 1983, American journal of hematology/oncology.

Oxygen affinity and stability of hemoglobin dunn (α6(A4)Asp→Asn): Use of isoelectric focusing in recognition of a new abnormal hemoglobin

S. Charache, B. Brimhall, G. Zaatari, 1980 .