Published in Arch Biochem Biophys on November 01, 1963
PROLONGED NEONATAL UNCONJUGATED HYPERBILIRUBINEMIA ASSOCIATED WITH BREAST FEEDING AND A STEROID, PREGNANE-3(ALPHA), 20(BETA)-DIOL, IN MATERNAL MILK THAT INHIBITS GLUCURONIDE FORMATION IN VITRO. J Clin Invest (1964) 2.60
The effect of steroids and nucleotidesoon solubilized bilirubin uridine diphosphate-glucuronyltransferase. Biochem J (1970) 1.15
Formation of bilirubin glucoside. Biochem J (1971) 0.96
TRANSIENT FAMILIAL NEONATAL HYPERBILIRUBINEMIA. J Clin Invest (1965) 0.88
Glucuronidation of 3-O-methylnoradrenaline, harmalol and some related compounds. Biochem J (1968) 0.81
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
A metal-filled microelectrode. Science (1953) 1.45
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
Effect of anabolic steroids on liver function tests and creatine excretion. JAMA (1961) 1.13
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
Site of origin and velocity of conduction of fibrillary potentials in denervated skeletal muscle. Am J Physiol (1954) 1.04
Birth weight in cystic fibrosis of the pancreas. Ann Hum Genet (1959) 1.04
The heterozygous carrier in galactosaemia. Nature (1958) 1.04
Erythrocyte electrolytes in muscle disease. J Lab Clin Med (1959) 1.03
POLYMYOSITIS AND OTHER DISEASES RESEMBLING MUSCULAR DYSTROPHY. Arch Intern Med (1965) 1.00
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
INHIBITORS OF GLUCURONYL TRANSFERASE IN THE NEWBORN. Ann N Y Acad Sci (1963) 0.94
Uptake and binding of thyroxine and triiodothyronine by rat diaphragm in vitro. Am J Physiol (1961) 0.94
Glucose-6-phosphate dehydrogenase deficiency in Taiwan. Am J Hum Genet (1963) 0.94
Hypervitaminosis D in monkeys; a clinical and pathologic study. Am J Pathol (1958) 0.93
Clinical course of hyperbilirubinemia in premature infants. A preliminary report. N Engl J Med (1960) 0.90
Thyroxine and triidothyronine turnover studies in dystrophia myotonica. J Clin Endocrinol Metab (1961) 0.90
On the hydrolysis and oxidation of glucuronolactone. Biochim Biophys Acta (1959) 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
The genetic mechanism of galactosaemia. Arch Dis Child (1960) 0.86
STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME. N Engl J Med (1964) 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
Effect of norethandrolone on serum enzyme levels. J Clin Endocrinol Metab (1958) 0.83
Prolonged survival of dystrophic mice treated with 17 alpha-ethyl-19-nortestosterone. Nature (1959) 0.82
Development of 5-hydroxytryptophan decarboxylase activity in rat kidney. Nature (1960) 0.82
The fate of sodium glucuronate and glucuronolactone in man. J Clin Invest (1956) 0.81
Inborn errors of carbohydrate metabolism. Diabetes (1961) 0.81
Modified resin method for determination of radioiodine conversion ratio. J Lab Clin Med (1960) 0.81
The interaction of a nonionic detergent with protein. I. Physical properties of the protein detergent complex. Arch Biochem Biophys (1961) 0.81
Determination of creatine in biological fluids. Biochem J (1957) 0.81
EFFECTS OF STEROIDS ON THE COURSE OF HEREDITARY MUSCULAR DYSTROPHY IN MICE. Am J Physiol (1964) 0.80
Further studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1960) 0.80
Blood glucose-6-phosphate in heterozygous carriers and patients with liver glycogen disease (Von Gierke's disease). Nature (1961) 0.80
Clinical management of phenylketonuria. Q Bull Northwest Univ Med Sch (1962) 0.80
Medical genetics. N Engl J Med (1960) 0.80
The interaction of a nonionic detergent with protein. II. Effects on a bovine plasma albumin-azomercurial complex. Arch Biochem Biophys (1961) 0.79
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
MECHANISMS FOR THE DECREASE OF BRAIN SEROTONIN. Nature (1963) 0.78
An inborn error of lipid metabolism. Pediatrics (1959) 0.78
Lipoprotein lipase in cystic fibrosis of the pancreas. J Lab Clin Med (1962) 0.78
Detection of heterozygous carriers in glycogen storage disease of the liver (von Gierke's disease). Nature (1959) 0.78
Medical genetics. N Engl J Med (1960) 0.78
Hypertension associated with renal neoplasm: report of two cases. Ann Intern Med (1954) 0.77
STUDIES ON INHIBITION OF BRAIN 5-HYDROXYTRYPTOPHAN DECARBOXYLASE BY PHENYLALANINE METABOLITES. Proc Soc Exp Biol Med (1965) 0.76
Studies on the heterozygous carrier in galactosemia. J Lab Clin Med (1959) 0.76
Recent developments in inborn errors of metabolism. Am J Public Health Nations Health (1960) 0.75
Activity of glucose-6-phosphate dehydrogenase in erythrocyes of patients with various abnormal hemoglobins. Pediatrics (1960) 0.75
Studies on the relation of mechanical fragility of erythrocytes to physiological jaundice. AMA Am J Dis Child (1953) 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
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
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
ESSENTIAL FAMILIAL HYPERLIPEDEMIA IN CHILDHOOD. I. CARBOHYDRATE-INDUCED HYPERLIPIDEMIA. Pediatrics (1964) 0.75
THIN-LAYER CHROMATOGRAPHIC ANALYSIS OF PLASMA PHOSPHOLIPIDS IN ESSENTIAL FAMILIAL HYPERLIPIDEMIA. J Lab Clin Med (1964) 0.75
A manometric assay for glucose-6-phosphate dehydrogenase. Clin Chim Acta (1961) 0.75
Galactosemia: clinical, genetic, and biochemical study. JAMA (1961) 0.75
Variability in the clinical manifestations of galactosemia. J Pediatr (1962) 0.75
The metabolism of indole-compounds in phenvlketonuria. Cereb Palsy Bull (1961) 0.75
Studies on erythroblastosis due to ABO incompatibility. AMA Am J Dis Child (1953) 0.75
Metabolism of 5-hydroxyindole compounds in experimentally produced phenylketonuric rats. Proc Soc Exp Biol Med (1961) 0.75
Diet in relation to hereditary metabolic disorders. Pediatr Clin North Am (1962) 0.75
ENZYMATIC OXIDATION OF GALACTOSE-6-PHOSPHATE. Nature (1964) 0.75
Recent developments in the study of hereditary diseases in children. Postgrad Med (1957) 0.75
Medical genetics. N Engl J Med (1960) 0.75
Genetic errors of metabolism and environmental interaction: a synthesis. Ann N Y Acad Sci (1961) 0.75
Recent advances in biochemical detection of heterozygous carriers in hereditary diseases. Metabolism (1960) 0.75
[Human biochemical genetics]. Duodecim (1962) 0.75
PARTIAL PURIFICATION OF HEXOSE-1-PHOSPHATE URIDYLTRANSFERASE FROM HUMAN RED CELLS. Biochim Biophys Acta (1965) 0.75