Published in Blood on May 01, 1951
INTRAUTERINE TRANSFUSION OF FOETUS IN HAEMOLYTIC DISEASE. Br Med J (1963) 4.69
First premarital screening of thalassaemia carriers in intermediate schools in Latium. J Med Genet (1978) 3.54
Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis. Am J Hum Genet (1953) 3.42
A Third Abnormal Hemoglobin Associated with Hereditary Hemolytic Anemia. Proc Natl Acad Sci U S A (1951) 3.22
Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies. Br Med J (1968) 2.87
Observations on the minor basic hemoglobin component in the blood of normal individuals and patients with thalassemia. J Clin Invest (1957) 2.84
The anemia of liver disease: observations on its mechanism. J Clin Invest (1955) 2.66
Abnormal rheology of oxygenated blood in sickle cell anemia. J Clin Invest (1970) 2.42
5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons. Proc Natl Acad Sci U S A (1982) 2.19
Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia. J Clin Invest (1968) 2.06
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation. J Clin Pathol (1972) 1.88
HUMAN HAEMOGLOBINS. J Med Genet (1965) 1.83
Expression of the sickle-cell gene in Africa. Br Med J (1955) 1.75
Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria. Am J Hum Genet (1966) 1.72
Screening for abnormal haemoglobins: a pilot study. Br Med J (1973) 1.72
Mechanical rotary device for plating out bacteria on solid medium. J Clin Pathol (1968) 1.67
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India. Indian J Hum Genet (2010) 1.61
THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS. Am J Hum Genet (1964) 1.60
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. Proc Natl Acad Sci U S A (1983) 1.60
BIOCHEMICAL POLYMORPHIC TRAITS IN A U. S. WHITE AND NEGRO POPULATION. Am J Hum Genet (1963) 1.58
INTRAUTERINE TRANSFUSION OF THE FOETUS IN HAEMOLYTIC DISEASE. Br Med J (1964) 1.55
Stimulation of fetal hemoglobin synthesis in baboons by hemolysis and hypoxia. Proc Natl Acad Sci U S A (1978) 1.52
Filter paper electrophoresis of human hemoglobin. J Clin Invest (1953) 1.51
Studies on the destruction of red blood cells. XII. Factors influencing the role of S hemoglobin in the pathologic physiology of sickle cell anemia and related disorders. J Clin Invest (1957) 1.42
Transplacental bleeding from the foetus. J Clin Pathol (1958) 1.41
Perinatal death from foetal exsanguination. Br Med J (1957) 1.38
Four haemoglobins in one individual. A study of the genetic interaction of Hb-G and Hb-C. Br Med J (1960) 1.35
Loci differentially affected by selection in two American black populations. Proc Natl Acad Sci U S A (1971) 1.31
The relationship of serum gamma-globulin concentration to malaria and sickling. J Clin Pathol (1960) 1.28
HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY. Br Med J (1964) 1.27
Haemoglobin Q-alpha-thalassaemia. Br Med J (1961) 1.25
Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin. Br Med J (1959) 1.23
Haemoglobin O in An Arab Family. Br Med J (1960) 1.23
Unusual haemoglobin variant in a Gujerati Indian. Br Med J (1957) 1.22
Studies of the incoporation of Fe59 into normal and abnormal hemoglobins. J Clin Invest (1959) 1.21
Hemoglobin Porto Alegre, a possible polymer of normal hemoglobin in a Caucasian Brazilian family. Am J Hum Genet (1963) 1.20
Some clinical, biochemical and genetic observations on hemoglobin C. J Clin Invest (1953) 1.19
Two families showing interaction of haemoglobin C or thalassaemia with high foetal haemoglobin in adults. Br Med J (1961) 1.19
The development of an acquired haemoglobin abnormality caused by thermal injury. J Clin Pathol (1960) 1.17
Date on the occurrence of hemoglobin C and other abnormal hemoglobins in some African populations. Am J Hum Genet (1956) 1.17
Haemoglobinopathies in immigrant families. Postgrad Med J (1965) 1.14
HUMAN HEMOGLOBIN GENE LINKAGE: REPORT OF A FAMILY WITH HEMOGLOBIN B2, HEMOGLOBIN S, AND BETA THALASSEMIA, INCLUDING A PROBABLE CROSSOVER BETWEEN THALASSEMIA AND DELTA LOCI. Am J Hum Genet (1965) 1.12
Haematological effects of chronic benzene poisoning in 217 workers. Br J Ind Med (1971) 1.10
Haemoglobin L; a new haemoglobin found in a Punjabi Hindu. Br Med J (1957) 1.10
Details of blood changes in 32 patients with pancytopenia associated with long-term exposure to benzene. Br J Ind Med (1972) 1.09
A report on the interlaboratory quantitation of haemoglobin A2 and haemoglobin F. J Clin Pathol (1973) 1.08
Foetal exsanguination associated with surgical induction of labour. Br Med J (1956) 1.06
Hemoglobin Hiroshima (beta-143 histidine--aspartic acid): a newly identified fast moving beta chain variant associated with increased oxygen affinity and compensatory erythremia. J Clin Invest (1969) 1.06
The frequency of elevations in the A and fetal hemoglobin fractions in the natives of Liberia and adjacent regions, with data on haptoglobin and transferrin types. Am J Hum Genet (1961) 1.06
Frequency of thalassemia in a sample of the Spanish population. Am J Hum Genet (1967) 1.05
STUDIES ON SEVERAL GENETIC HEMATOLOGICAL TRAITS OF THE MEXICAN POPULATION. 8. HEMOGLOBIN S, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, AND OTHER CHARACTERISTICS IN A MALARIAL REGION. Am J Hum Genet (1965) 1.05
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. J Med Genet (1972) 1.05
THE THALASSAEMIA TRAIT IN AN ENGLISH FAMILY. J Clin Pathol (1963) 1.04
Quantitative determination of haemoglobin A2 using paper electrophoresis. J Clin Pathol (1961) 1.04
HAEMOGLOBIN H DISEASE IN AN ENGLISH FAMILY. Br Med J (1964) 1.03
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India. Indian J Hum Genet (2010) 1.03
Changing blood picture in sickle-cell anaemia from shortly after birth to adolescence. J Clin Pathol (1976) 1.02
Studies on the haemoglobin of newborn Nigerians. Br Med J (1960) 1.01
Persistent fetal haemoglobin and falsely high glycosylated haemoglobin levels. Br Med J (Clin Res Ed) (1984) 1.01
THALASSAEMIA IN SCOTS. J Clin Pathol (1963) 1.00
Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin. J Med Genet (1977) 0.99
The effect of methemoglobin formation in sickle cell disease. J Clin Invest (1961) 0.99
Between two worlds. Am J Hum Genet (1966) 0.99
Haemoglobinopathies and malaria in Thailand. Bull World Health Organ (1969) 0.99
A partial D-trisomy-normal mosaic female. J Med Genet (1971) 0.99
A study of the survival rate of cases of sickle-cell anaemia. Br Med J (1957) 0.99
Sickle-cell anaemia complicated by megaloblastic anaemia of infancy. Br Med J (1960) 0.98
Acute acquired haemolytic anaemia associated with polyagglutination. Arch Dis Child (1969) 0.97
A critical review of human haemoglobin variants. II. Individual haemoglobins. J Clin Pathol (1959) 0.96
Hemoglobin abnormalities in neoplastic hematological disorders. Can Med Assoc J (1973) 0.96
Blood groups, haemoglobins, and thalassaemia in Turks in southern Turkey and Eti-Turks. Br Med J (1958) 0.95
Stanleyville I and II: two new variants of adult haemoglobin. Br Med J (1959) 0.94
Homozygous beta thalassaemia in Liberia. J Med Genet (1975) 0.93
Ligand kinetics of hemoglobin S containing erythrocytes. Proc Natl Acad Sci U S A (1977) 0.93
Control of the simian fetal hemoglobin switch at the progenitor cell level. J Clin Invest (1981) 0.93
Combinations of high levels of hemoglobin F with haemoglobins A, S, and C in Ghana. Br Med J (1962) 0.93
The effects of deoxygenation of adult and fetal hemoglobin on the synthesis of red cell 2,3-diphosphoglycerate and its in vivo consequences. J Clin Invest (1970) 0.92
MALARIA AND STRESS IN RELATION TO HAEMOGLOBINS S AND C. Br Med J (1963) 0.91
Sickling times of individual erythrocytes at zero Po2. J Clin Invest (1975) 0.91
Abnormal hemoglobins in a Brazilian Negro population. Am J Hum Genet (1962) 0.91
Structural and functional studies on hemoglobin Bethesda (alpha2beta2 145His), a varient associated with compensatory erythrocytosis. J Clin Invest (1972) 0.91
Foetal haemoglobin in haemolytic disease of the newborn. Arch Dis Child (1961) 0.90
The hereditary anemias. Bull N Y Acad Med (1954) 0.90
A simple micromethod for the measurement of fetal haemoglobin. J Clin Pathol (1975) 0.90
Hereditary elliptocytosis in two Maltese families. J Clin Pathol (1961) 0.90
Hemoglobin Hasharon (alpha-2-47 his(CD5)beta-2): a hemoglobin found in low concentration. J Clin Invest (1969) 0.89
Studies on thalassemia, glucose-6-phosphate dehydrogenase deficiency, and sickle cell trait in the Province of Huelva (Spain). Am J Hum Genet (1969) 0.89
Thalassaemia and hydrops foetalis-family studies. Br Med J (1967) 0.88
Haemoglobin E in Burmese; two cases of haemoglobin E disease. Br Med J (1956) 0.88
Thalassaemia minor in an English family. Br Med J (1962) 0.88
Haemoglobin E and alpha-Thalassaemia. Br Med J (1967) 0.87
Thalassemia in Canadians. Can Med Assoc J (1967) 0.87
Haemoglobin H disease in Arabs in Kuwait. J Clin Pathol (1969) 0.87
Localization of genes on chromosome 13: analysis of two kindreds. Am J Hum Genet (1968) 0.87
A family illustrating the double inheritance of the sickle cell trait and of Mediterranean anaemia. J Clin Pathol (1954) 0.86
Hemoglobin Yoshizuka (G10(108)beta asparagine--aspartic acid): a new variant with a reduced oxygen affinity from a Japanese family. J Clin Invest (1969) 0.86
The disappearance of foetal haemoglobin in congenital cyanotic heart disease. Arch Dis Child (1958) 0.85
Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes. J Clin Invest (1968) 0.84
HEMOGLOBIN C DISEASE IN A SICILIAN-CANADIAN FAMILY. Can Med Assoc J (1963) 0.84
OBSERVATIONS ON THE RESISTANCE IN HB E THALASSAEMIA DISEASE TO INDUCED INFECTION WITH PLASMODIUM VIVAX. Bull World Health Organ (1964) 0.83
Studies on abnormal hemoglobins. II. Their identification by means of the method of fractional denaturation. Blood (1951) 3.25
Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance. Blood (1953) 2.06
Immunologic studies of hemoglobins. III. Fetal hemoglobin changes in the circulation of pregnant women. Blood (1955) 1.63
Immunologic studies of hemoglobins. II. Quantitative precipitin test using anti fetal hemoglobin sera. Blood (1953) 1.59
The life span of the elliptocyte; hereditary elliptocytosis and its relationship to other familial hemolytic diseases. Blood (1954) 1.55
Acanthrocytosis; a genetic erythrocytic malformation. Blood (1952) 1.43
Acute erythroblastopenia in sickle-cell anemia and infectious mononucleosis. AMA Am J Dis Child (1951) 1.42
Danger of dicumarol treatment in pregnancy. J Am Med Assoc (1949) 1.41
The human hemoglobins in health and disease. N Engl J Med (1955) 1.38
Aplastic crisis in sickle cell anemia; a study of its mechanism and its relationship to other types of hemolytic crises. J Lab Clin Med (1950) 1.37
ABSORPTION OF FLUORIDE AND CHLORIDE BY BARLEY ROOTS. Plant Physiol (1965) 1.37
Studies on hemoglobin E. I. The clinical, hematologic, and genetic characteristics of the hemoglobin E syndromes. J Lab Clin Med (1956) 1.31
Thrombotic thrombocytopenic purpura. II. Studies on the hemolytic syndrome in this disease. Blood (1950) 1.27
Studies on abnormal hemoglobins. IV. Persistence of fetal hemoglobin in the erythrocytes of normal children. Pediatrics (1952) 1.27
THE AMINO ACID COMPOSITION OF HEMOGLOBIN. 3. A QUALITATIVE METHOD FOR IDENTIFYING ABNORMALITIES OF THE POLYPEPTIDE CHAINS OF HEMOGLOBIN. Blood (1964) 1.25
Circulating anticoagulants in hemophilia and in hemophilia-like disease. Blood (1950) 1.25
Pseudohemophilia type B; hereditary hemorrhagic diathesis characterized by prolonged bleeding time and decrease in antihemophilic factor. AMA Arch Intern Med (1956) 1.19
Regulation of human plasma fluoride concentration. J Appl Physiol (1960) 1.19
Huntington's chorea in the Chinese. Br Med J (1962) 1.15
Studies on abnormal hemoglobins. XII. Terminal and free amino groups of various types of human hemoglobin. Arch Biochem Biophys (1955) 1.13
[Anatomical and histological studies on arthroplasty with plexiglass endoprosthesis; possibilities and limitations of reformation of joints]. Arch Orthop Unfallchir (1956) 1.13
The human hemoglobins in health and disease. N Engl J Med (1955) 1.11
The amino acid composition of hemoglobin. II. Analytical technics. Blood (1961) 1.09
Variable manifestations of plasma thromboplastin component deficiency. J Lab Clin Med (1955) 1.04
Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis. Blood (1955) 1.03
Polycythemia with fibroids. J Am Med Assoc (1955) 1.02
Starch block electrophoretic studies of human hemoglobin solutions. I. Technic and results in the normal adult. Blood (1958) 1.00
Distribution and excretion of radiofluoride in the human. Proc Soc Exp Biol Med (1960) 0.99
PLASMA FLUORIDE CONCENTRATIONS ON PATIENTS TREATED WITH SODIUM FLUORIDE. J Clin Invest (1964) 0.98
Studies on abnormal hemoglobins. IX. Pure (homozygous) hemoglobin C disease. Blood (1954) 0.97
HETEROZYGOUS BETA-THALASSEMIA IN ASSOCIATION WITH HEREDITARY ELLIPTOCYTOSIS: A FAMILY STUDY. Blood (1965) 0.96
Hemoglobin E, a hereditary abnormality of human hemoglobin. Science (1954) 0.95
The pathogenesis of sickle cell anemia; a review. Am J Clin Pathol (1951) 0.95
A METHOD FOR THE QUANTITATIVE DETERMINATION OF HGB A2. Ann N Y Acad Sci (1964) 0.95
The L.E.-cell phenomenon in chronic hepatic disease. N Engl J Med (1956) 0.93
Hageman factor (HF) deficiency. Blood (1956) 0.92
Studies on hemoglobin E. II. The incidence of hemoglobin E in Thailand. J Lab Clin Med (1956) 0.92
Studies on abnormal hemoglobins. VII. The composition of the non-S hemoglobin fraction in sickle-cell anemia bloods; a comparative quantitative study by the methods of electrophoresis and alkali denaturation. J Lab Clin Med (1953) 0.90
Studies on human myoglobin. II. Fetal myoglobin: its identification and its replacement by adult myoglobin during infancy. Blood (1955) 0.90
Hereditary hemolytic disorders associated with abnormal hemoglobins. Am J Med (1955) 0.89
Immunologic studies of hemoglobins. I. The production of anti-hemoglobin sera and their immunologic characteristics. Blood (1953) 0.89
Radiofluoride distribution in tissues of normal and nephrectomized rats. Proc Soc Exp Biol Med (1960) 0.88
Thrombotic thrombocytopenic purpura; hemorrhagic diathesis with generalized platelet thromboses. Blood (1947) 0.87
Determinations of fetal hemoglobin in whole blood, using a modified alkali denaturation test. Am J Clin Pathol (1958) 0.86
The distribution of the thalassemia gene: a historical review. Blood (1959) 0.86
Thrombotic thrombocytopenic purpura. Adv Intern Med (1954) 0.86
Therapy of chronic ulceration of the legs associated with sickle cell anemia. J Am Med Assoc (1954) 0.85
The human hemoglobins in health and disease. N Engl J Med (1955) 0.85
Rates of transcapillary movement of calcium and sodium and of calcium exchange by the skeleton. Am J Physiol (1952) 0.85
Hemolytic mechanism in sickle cell-Hgb C disease. Proc Soc Exp Biol Med (1955) 0.83
The relative binding of calcium and strontium with serum proteins and other substances. Proc Soc Exp Biol Med (1962) 0.83
Endogenous and biliary excretion of calcium-45 and strontium-89. Arch Biochem Biophys (1957) 0.83
Rapid test for the demonstration of sickle cells and its clinical significance. J Am Med Assoc (1948) 0.83
The developing (Coombs) test in spherocytic hemolytic anemias; its significance for the pathophysiology of spherocytosis and splenic hemolysis. J Lab Clin Med (1949) 0.83
Retention and turnover of radiocalcium by the skeleton of large rats. Proc Soc Exp Biol Med (1951) 0.82
ANALYSIS OF ECTOPIC BONE IN OSTEOMA CUTIS. Arch Dermatol (1963) 0.82
MICRODETERMINATION OF CALCIUM IN BIOLOGICAL MATERIALS. Anal Biochem (1964) 0.82
Distribution, migration and binding of whole blood fluoride evaluated with radiofluoride. Am J Physiol (1960) 0.81
[Pathologic-anatomic knowledge from the progress in surgery]. Langenbecks Arch Klin Chir Ver Dtsch Z Chir (1955) 0.81
A new variant of hemoglobin M disease: hemoglobin M-Chicago. J Lab Clin Med (1962) 0.81
Plasma thromboplastin antecedent deficiency. AMA Arch Intern Med (1955) 0.81
Skeletal calcium turnover in nongrowing rats. Proc Soc Exp Biol Med (1953) 0.81
The hemoglobin D syndromes. Blood (1958) 0.81
Rapid demonstration of A2 hemoglobin by means of agar gel electrophoresis. Am J Clin Pathol (1960) 0.80
The experimental production of Heinz bodies in various hemoglobinopathies and the thalassemic syndromes. J Lab Clin Med (1958) 0.80
An unusual circulating anticoagulant in systemic lupus erythematosus. Acta Haematol (1956) 0.80
Anaphylactic reaction following injection of heparin. N Engl J Med (1950) 0.79
Studies on abnormal hemoglobins. X. A new syndrome: hemoglobin C-thalassemia disease. Blood (1954) 0.79
On the prevalence of hemoglobin D in the American Negro. Blood (1956) 0.78
Studies on human myoglobin. I. Myoglobin in sickle cell disease. Blood (1955) 0.78
[Physiopathic and psychopathic contractures, an attempt at differential diagnosis]. Lyon Chir (1954) 0.77
THE AMINO ACID COMPOSITION OF HEMOGLOBIN. VI. SEPARATION OF THE TRYPTIC PEPTIDES OF HEMOGLOBIN KNOXVILLE NO. I ON DOWEX-I X-2 AND SEPHADEX. Biochim Biophys Acta (1965) 0.76
Hemoglobin patterns in American Indians. Science (1959) 0.76
Molybdenum metabolism and interrelationships with copper and phosphorus. J Biol Chem (1949) 0.76
Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia. Blood (1952) 0.76
A microhemolyzing technic for preparing solutions of hemoglobin for paper electrophoretic analysis. Am J Clin Pathol (1958) 0.76
SODIUM FLUORIDE AND CELL GROWTH. Br Med J (1965) 0.75
SODIUM FLUORIDE AND CELL GROWTH. Br Med J (1965) 0.75
Effect of platelet extract on hemophilic blood. J Clin Invest (1951) 0.75
[Psychotic and neurotic syndromes in brain tumors]. Strasb Med (1953) 0.75
[Epithelioma of pituitary; clinical and postoperative data]. Neurochirurgie (1955) 0.75
[Pathological alcoholic intoxications and acute alcoholic psychoses]. Strasb Med (1955) 0.75
[Manifestations of hysteria and disorders of consciousness in the course of evolutive cerebral lesions; clinical and electroencephalographic studies of 4 similar cases]. Cah Psychiatr (1956) 0.75
[Clinical results in psychosurgery, statistical report]. Rev Neurol (Paris) (1953) 0.75
[Electroencephalographic disturbances in relation to paroxysmal disorders of consciousness, with cyclic evolution; presentation of a syndrome of probable encephalitic origin]. Rev Neurol (Paris) (1956) 0.75
[The syndrome of dementia presenilis: comparison of clinical and psychometric data]. Cah Psychiatr (1956) 0.75
[Pathological anatomy and histopathology of renal tuberculosis after chemotherapy as studied on pole resections]. Urol Int (1956) 0.75
[Convulsive crisis, crepuscular incidents, contracture and edema of upper extremities in a patient with mental debility]. Cah Psychiatr (1955) 0.75