Published in AMA J Dis Child on April 01, 1959
Thalassaemia. Postgrad Med J (1965) 0.75
Haemoglobin Lepore in Cyprus. J Med Genet (1975) 0.75
Haemoglobin LeporeBoston in a Turkish family. J Med Genet (1976) 0.75
THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION. J Pediatr (1964) 4.12
Autoerythrocyte sensitization; a form of purpura producing painful bruising following autosensitization to red blood cells in certain women. Blood (1955) 3.69
Anaphylactoid purpura in children (Schonlein-Henoch syndrome): review with a follow-up of the renal complications. AMA J Dis Child (1960) 3.04
Temporary remissions in acute leukemia in children produced by folic acid antagonist, 4-aminopteroyl-glutamic acid. N Engl J Med (1948) 2.81
Congenital (erythroid) hypoplastic anemia. A 25-year study. Am J Dis Child (1961) 2.61
Recommendations for the nomenclature of hemoglobins. J Biol Chem (1961) 2.56
Erythroblastosis fetalis. Pediatrics (1952) 2.36
Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus. N Engl J Med (1952) 2.23
Coagulation defects with intrauterine death from Rh isosensitization. Am J Obstet Gynecol (1950) 1.90
Erythroblastosis fetalis; the value of blood from female donors for exchange transfusion. N Engl J Med (1949) 1.83
The electrophoretic and spectroscopic characterization of Hgb M. Blood (1958) 1.78
Identification of the abnormal polypeptide chain of hemoglobin G-Ib. J Mol Biol (1960) 1.69
Maternal afibrinogenemia associated with long-standing intrauterine fetal death. Am J Obstet Gynecol (1953) 1.68
Suspected correlation between blood-group frequency and pituitary adenomas. Science (1956) 1.68
Erythrocyte acid phosphomonesterase and glucose-6-phosphate dehydrogenase deficiency in Caucasians. Science (1963) 1.64
Effects of corticosteroids on coagulation of the blood. Nature (1962) 1.60
Chemical studies of several varieties of Hb M. Proc Natl Acad Sci U S A (1961) 1.57
The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin. Blood (1958) 1.57
In vitro erythrophagocytosis in acquired hemolytic anemia. Blood (1952) 1.57
Serum bilirubin levels in the newborn infant. J Pediatr (1953) 1.51
Prolonged obstructive jaundice in infancy. I. General survey of 156 cases. Pediatrics (1952) 1.42
Geographic blood group variability in the United States. J Am Med Assoc (1951) 1.41
Congenital afibrinogenemia; a study of some basic aspects of coagulation. Blood (1954) 1.41
Testosterone-induced remission in aplastic anemia of both acquired and congenital types. Further observations in 24 cases. N Engl J Med (1961) 1.39
Testosterone-induced remission in aplastic anemia. AMA J Dis Child (1959) 1.37
Erythroblastosis fetalis. II. Prognosis in relation to history, maternal titer and length of fetal gestation. Pediatrics (1950) 1.36
ISOIMMUNE NEONATAL THROMBOCYTOPENIC PURPURA. CLINICAL AND THERAPEUTIC CONSIDERATIONS. Blood (1964) 1.34
A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait. Blood (1958) 1.32
SUCCESSFUL TREATMENT OF PNEUMOCYSTIS CARINII PNEUMONITIS IN A PATIENT WITH CONGENITAL HYPOGAMMAGLOBULINEMIA. N Engl J Med (1965) 1.27
Congenital (erythroid) hypoplastic anemia: cortisone treated. Am J Dis Child (1961) 1.27
Erythroblastosis fetalis. IX. The problems of stillbirth. N Engl J Med (1954) 1.25
CHLORAMPHENICOL IN BLOOD: SIMPLE CHEMICAL ESTIMATIONS IN PATIENTS RECEIVING MULTIPLE ANTIBIOTICS. Science (1964) 1.25
Erythroblastosis fetalis. VII. Treatment with exchange transfusion. N Engl J Med (1951) 1.25
Purpura in infants and children; its natural history. AMA Am J Dis Child (1953) 1.24
Medicolegal applications of blood grouping. N Engl J Med (1954) 1.23
Erythroblastosis fetalis. VI. Prevention of kernicterus. AMA Am J Dis Child (1950) 1.22
On the inheritance of the antigen f of the Rh complex. Am J Hum Genet (1954) 1.22
Pheochromocytoma in children; report of three familial cases in two unrelated families. Pediatrics (1957) 1.21
Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia. Pediatrics (1959) 1.20
"Enclosed" hemorrhage and neonatal jaundice. Am J Dis Child (1961) 1.18
Immunoreactions involving platelet. VI. Reactions of maternal isoantibodies responsible for neonatal purpura. Differentiation of a second platelet antigen system. J Clin Invest (1962) 1.17
Rh and other blood groups. N Engl J Med (1949) 1.17
THE GASTROINTESTINAL EFFECTS OF IRON-DEFICIENCY ANEMIA. Pediatrics (1964) 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
The effect of adrenocorticotrophic hormone (ACTH) in idiopathic acquired hemolytic anemia as related to the hemolytic mechanisms. J Lab Clin Med (1951) 1.11
Leukocytic inclusions--Dohle bodies--associated with platelet abnormality (the May-Hegglin anomaly). Report of a family and review of the literature. Blood (1962) 1.10
Inherited electrophoretic hemoglobin patterns among 20 inbred strains of mice. Science (1958) 1.09
Report of a second example of the Rh agglutinogen cv, with some comments on its relation to the agglutinogen f. Science (1953) 1.09
EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES. N Engl J Med (1964) 1.08
Second spectroscopically abnormal methemoglobin associated with hereditary cyanosis. Science (1959) 1.08
Erythroblastosis fetalis. I. Problems in the interpretation of changing mortality in erythroblastosis fetalis. Pediatrics (1950) 1.06
Erythroblastosis fetalis. IV. Further observations on kernicterus. Pediatrics (1950) 1.04
Fetomaternal transfusion. AMA J Dis Child (1959) 1.02
Haemophilia and related haemorrhagic disorders. Practitioner (1957) 1.01
Erythroblastosis foetalis or haemolytic disease of the newborn. Proc R Soc Med (1947) 1.00
Use of the plasma acid phosphatase value in the differentiation of thrombocytopenic states. N Engl J Med (1963) 1.00
Anemia associated with protein deficiency. A study of 2 cases with cystic fibrosis. J Pediatr (1961) 0.96
Effects of early feeding of strained meat to prematurely born infants. Pediatrics (1952) 0.96
Hemoglobin M. Science (1957) 0.96
Observations on the new Rh agglutinin anti-f. Blood (1954) 0.95
Treatment of classic hemophilia: the use of fibrinogen rich in factor VIII for hemorrhage and for surgery. N Engl J Med (1961) 0.95
ERYTHROCYTE PYRUVATE KINASE DEFICIENCY RESULTING IN CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA. N Engl J Med (1963) 0.95
Erythroblastosis fetalis. N Engl J Med (1957) 0.94
Biopsy of bone marrow with the Silverman needle in children. Pediatrics (1960) 0.94
Erythroblastosis fetalis. III. Prognosis in relation to clinical and serologic manifestations at birth. Pediatrics (1950) 0.93
Haptoglobin patterns in cord blood serums. Nature (1961) 0.91
Alkali-resistant hemoglobin in aplastic anemia of both acquired and congenital types. N Engl J Med (1962) 0.91
Vitamin B12 deficiency associated with disease of the small intestine. Observations on an infant following extensive small bowel resection. J Pediatr (1960) 0.91
THE BINDING OF CR51 TO HEMOGLOBIN. I. IN VITRO STUDIES. Blood (1963) 0.89
Starch block electrophoresis of hemoglobin. U S Armed Forces Med J (1959) 0.89
Genetical evidence for synthesis of transferrin in the foetus. Nature (1961) 0.89
Portal hypertension a complication of umbilical vein catheterization. Pediatrics (1963) 0.89
Rh and other blood groups. N Engl J Med (1949) 0.88
EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. II. MEASUREMENTS OF ERYTHROCYTE GLUCOSE CONSUMPTION, POTASSIUM FLUX AND ADENOSINE TRIPHOSPHATE STABILITY. N Engl J Med (1965) 0.88
PERNICIOUS ANEMIA WITH NEUROLOGIC INVOLVEMENT IN CHILDHOOD: REPORT OF A CASE WITH EMPHASIS ON DANGERS OF FOLIC ACID THERAPY. J Pediatr (1964) 0.88
Turnover among hospital staff nurses. Nurs Outlook (1958) 0.86
Inheritance of the human blood group antigen JKa. Nature (1951) 0.86
NORMAL RESPONSE OF SICKLE CELL ANEMIA PATIENTS TO IMMUNIZATION WITH SALMONELLA VACCINES. J Pediatr (1965) 0.85
Erythroblastosis fetalis: serum bilirubin. AMA Am J Dis Child (1952) 0.85
The inadequacies of routine bleeding and clotting times. N Engl J Med (1958) 0.84
Erythroblastosis fetalis. N Engl J Med (1957) 0.84
Prevention of kernicterus; management of erythroblastosis fetalis according to current knowledge. J Am Med Assoc (1954) 0.84
Erythrocyte glycolysis in erythroblastotic newborns. Erythrocyte glycolysis also in Rh-positive red cells coated with anti-D antibodies. AMA J Dis Child (1960) 0.83
Congenital hypoplastic anemia. Pediatrics (1957) 0.83
Skull changes in infants with chronic iron-deficiency anemia. N Engl J Med (1960) 0.82
Erythrokinetics in thalassemia. II. Studies in Lepore trait and hemoglobin H disease. J Lab Clin Med (1962) 0.82
MALIGNANT PHEOCHROMOCYTOMA. REPORT OF A CASE IN A 12-YEAR-OLD GIRL. Pediatrics (1963) 0.82
Erythrokinetic studies in thalassemia trait. J Lab Clin Med (1960) 0.81
A method for the determination of gentisic acid in serum. J Biol Chem (1951) 0.81
The production and proper use of Rh typing reagents. Am J Public Health Nations Health (1948) 0.81
Gross structure of haemoglobin A3 and the nature of its binding to chromium-51. Nature (1963) 0.80
HEREDITARY EOSINOPHILIA: REPORT OF A FAMILY AND REVIEW OF THE LITERATURE. Am J Hum Genet (1964) 0.80
Replacement transfusion as a treatment for erythroblastosis fetalis. Pediatrics (1948) 0.79