Published in N Engl J Med on June 23, 1960
Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria. Nature (1956) 2.98
Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus. N Engl J Med (1952) 2.23
A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria. Pediatrics (1958) 2.02
Variability in the clinical manifestations of galactosemia. J Pediatr (1961) 1.64
The laboratory detection of heterozygotes. Am J Hum Genet (1957) 1.58
Gamma globulin in the prevention of infectious hepatitis; studies on the use of small doses in family outbreaks. N Engl J Med (1954) 1.56
Serum bilirubin levels in the newborn infant. J Pediatr (1953) 1.51
Pathogenetic problems in phenylketonuria. Am J Med (1957) 1.46
Prolonged obstructive jaundice in infancy. IV. Neonatal hepatitis. AMA Am J Dis Child (1954) 1.38
Prolonged obstructive jaundice in infancy. V. The genetic components in neonatal hepatitis. AMA J Dis Child (1958) 1.37
Family outbreaks of infectious hepatitis; prophylactic use of gamma globulin. N Engl J Med (1953) 1.34
Inhibition of glucuronosyl transferase by progestational agents from serum of pregnant women. Nature (1960) 1.25
A case of phenylketonuria with borderline intelligence. AMA J Dis Child (1957) 1.25
Serum phenylalanine and tyrosine levels in the newborn infant. N Engl J Med (1962) 1.25
Detection of the heterozygous carriers of phenylketonuria. Lancet (1956) 1.23
SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA. JAMA (1964) 1.20
Studies on linkage between phenylketonuria and the blood groups. Am J Hum Genet (1960) 1.20
Epinephrine metabolism in phenylketonuria. Proc Soc Exp Biol Med (1962) 1.08
Birth weight in infants of diabetic mothers. Ann Hum Genet (1957) 1.08
INHIBITION OF GLUCURONOSYL TRANSFERASE BY STEROID HORMONES. Arch Biochem Biophys (1963) 1.05
Birth weight in cystic fibrosis of the pancreas. Ann Hum Genet (1959) 1.04
The heterozygous carrier in galactosaemia. Nature (1958) 1.04
Studies on the genetic mechanism of cystic fibrosis of the pancreas. AMA J Dis Child (1959) 0.99
The dietary phenylalanine requirements and tolerances of phenylketonuric patients. AMA J Dis Child (1957) 0.98
Glucose-6-phosphate dehydrogenase deficiency in Taiwan. Am J Hum Genet (1963) 0.94
INHIBITORS OF GLUCURONYL TRANSFERASE IN THE NEWBORN. Ann N Y Acad Sci (1963) 0.94
Clinical course of hyperbilirubinemia in premature infants. A preliminary report. N Engl J Med (1960) 0.90
Coproporphyrin studies in children. I. Urinary coproporphyrin excretion in normal children. Proc Soc Exp Biol Med (1954) 0.89
Galactosemia: a study of twenty-seven kindreds in North America. Ann Hum Genet (1962) 0.89
Experimental studies on blood-spinal fluid barrier for bilirubin. J Lab Clin Med (1959) 0.88
THE INFLUENCE OF SERUM BILIRUBIN LEVELS UPON THE ULTIMATE DEVELOPMENT OF LOW BIRTHWEIGHT INFANTS. J Ment Defic Res (1965) 0.87
STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME. N Engl J Med (1964) 0.86
The genetic mechanism of galactosaemia. Arch Dis Child (1960) 0.86
Homologous serum-hepatitis following the use of fraction IV prepared from postpartum plasma; a report of four cases. Am J Med Sci (1953) 0.86
The genetic mechanism of idiopathic hyperlipemia. N Engl J Med (1957) 0.85
Pregnancy in the diabetic mother with nephritis. Lancet (1957) 0.84
BRAIN SEROTONIN IN EXPERIMENTAL TYROSINOSIS. Nature (1964) 0.84
A controlled study on effect of promethazine hydrochloride and meperidine hydrochloride upon serum billirubin levels in the newborn infant. J Pediatr (1963) 0.83
Development of 5-hydroxytryptophan decarboxylase activity in rat kidney. Nature (1960) 0.82
Inborn errors of carbohydrate metabolism. Diabetes (1961) 0.81
Further studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1960) 0.80
Medical genetics. N Engl J Med (1960) 0.80
Clinical management of phenylketonuria. Q Bull Northwest Univ Med Sch (1962) 0.80
Blood glucose-6-phosphate in heterozygous carriers and patients with liver glycogen disease (Von Gierke's disease). Nature (1961) 0.80
Lipoprotein lipase in cystic fibrosis of the pancreas. J Lab Clin Med (1962) 0.78
Viral hepatitis. N Engl J Med (1953) 0.78
Studies on mechanism for decreased lipoprotein lipase in cystic fibrosis of the pancrease. J Pediatr (1963) 0.78
Detection of heterozygous carriers in glycogen storage disease of the liver (von Gierke's disease). Nature (1959) 0.78
An inborn error of lipid metabolism. Pediatrics (1959) 0.78
MECHANISMS FOR THE DECREASE OF BRAIN SEROTONIN. Nature (1963) 0.78
Medical genetics. N Engl J Med (1960) 0.78
Studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1959) 0.76
STUDIES ON INHIBITION OF BRAIN 5-HYDROXYTRYPTOPHAN DECARBOXYLASE BY PHENYLALANINE METABOLITES. Proc Soc Exp Biol Med (1965) 0.76
Recent developments in inborn errors of metabolism. Am J Public Health Nations Health (1960) 0.75
Diet in relation to hereditary metabolic disorders. Pediatr Clin North Am (1962) 0.75
A manometric assay for glucose-6-phosphate dehydrogenase. Clin Chim Acta (1961) 0.75
The metabolism of indole-compounds in phenvlketonuria. Cereb Palsy Bull (1961) 0.75
ENZYMATIC OXIDATION OF GALACTOSE-6-PHOSPHATE. Nature (1964) 0.75
Galactosemia: clinical, genetic, and biochemical study. JAMA (1961) 0.75
Variability in the clinical manifestations of galactosemia. J Pediatr (1962) 0.75
ESSENTIAL FAMILIAL HYPERLIPEDEMIA IN CHILDHOOD. I. CARBOHYDRATE-INDUCED HYPERLIPIDEMIA. Pediatrics (1964) 0.75
Prolonged obstructive jaundice in infancy. AMA Am J Dis Child (1952) 0.75
Activity of glucose-6-phosphate dehydrogenase in erythrocyes of patients with various abnormal hemoglobins. Pediatrics (1960) 0.75
Coproporphyrin studies in children. 2. Erythrocyte coproporphyrin and protoporphyrin levels in normal infants and children. Proc Soc Exp Biol Med (1954) 0.75
Studies on the relation of mechanical fragility of erythrocytes to physiological jaundice. AMA Am J Dis Child (1953) 0.75
PARTIAL PURIFICATION OF HEXOSE-1-PHOSPHATE URIDYLTRANSFERASE FROM HUMAN RED CELLS. Biochim Biophys Acta (1965) 0.75
[Human biochemical genetics]. Duodecim (1962) 0.75
Recent advances in biochemical detection of heterozygous carriers in hereditary diseases. Metabolism (1960) 0.75
Medical genetics. N Engl J Med (1960) 0.75
The excretion of 5-hydroxyindoleacetic acid in the heterozygous carrier for phenylketonuria. J Ment Defic Res (1961) 0.75
Genetic errors of metabolism and environmental interaction: a synthesis. Ann N Y Acad Sci (1961) 0.75
Metabolism of 5-hydroxyindole compounds in experimentally produced phenylketonuric rats. Proc Soc Exp Biol Med (1961) 0.75
Sodium glucuronate and glucuronolactone in bilirubin conjugation and formation of borneol glucuronide. Am J Physiol (1959) 0.75
Studies of the mechanical fragility of erythrocytes. II. Relation to physiologic jaundice of the newborn infant. Pediatrics (1954) 0.75
BILIRUBIN METABOLISM. Pediatr Clin North Am (1965) 0.75
Recent developments in the study of hereditary diseases in children. Postgrad Med (1957) 0.75
THIN-LAYER CHROMATOGRAPHIC ANALYSIS OF PLASMA PHOSPHOLIPIDS IN ESSENTIAL FAMILIAL HYPERLIPIDEMIA. J Lab Clin Med (1964) 0.75
Studies on erythroblastosis due to ABO incompatibility. AMA Am J Dis Child (1953) 0.75