Published in J Am Acad Dermatol on March 01, 1981
Iatrogenic skin lesions in phenylketonuric children due to a low tyrosine intake. J Inherit Metab Dis (1989) 0.75
Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study. Circulation (1998) 2.88
Cystathionine beta-synthase mutations in homocystinuria. Hum Mutat (1999) 1.96
Multiple hamartoma syndrome (Cowden's disease). Arch Dermatol (1972) 1.79
Obesity and leanness at birth and their relationship to body habitus in later childhood. Pediatrics (1975) 1.78
ABO blood group, other risk factors and incidence of venous thromboembolism: the Longitudinal Investigation of Thromboembolism Etiology (LITE). J Thromb Haemost (2007) 1.59
Homotransplantation of the liver in a patient with hepatoma and hereditary tyrosinemia. J Pediatr (1978) 1.53
The umbilical cord complications of true knots, nuchal coils, and cords around the body. Report from the collaborative study of cerebral palsy. Am J Obstet Gynecol (1966) 1.50
First-trimester chorionic gonadotropin measurements as an aid in the diagnosis of early pregnancy disorders. Am J Obstet Gynecol (1978) 1.46
Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet (1993) 1.38
Endometrial biopsy in the luteal phase of the cycle of conception. Fertil Steril (1971) 1.38
In vivo chloroquine-induced inhibition of insulin degradation in a diabetic patient with severe insulin resistance. Diabetes (1984) 1.30
Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation. Am J Hum Genet (1971) 1.21
Isozymes of rabbit phosphofructokinase. Electrophoretic and immunochemical studies. J Biol Chem (1973) 1.20
Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantation. N Engl J Med (1990) 1.19
A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis (2001) 1.15
Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuria. Hum Mol Genet (1997) 1.13
Physical and mental status at 4 years of age of survivors of the respiratory distress syndrome. Follow-up report from the collaborative study. J Pediatr (1975) 1.13
Six new mutations in the ornithine transcarbamylase gene detected by single-strand conformational polymorphism. Pediatr Res (1992) 1.12
The effects of a pacifying stimulus on behavioral and adrenocortical responses to circumcision in the newborn. J Am Acad Child Psychiatry (1984) 1.10
Hypoplastic enamel, onycholysis, and hypohidrosis inherited as an autosomal dominant trait. A review of ectodermal dysplasia syndromes. Oral Surg Oral Med Oral Pathol (1975) 1.08
Neonatal serum bilirubin levels related to cognitive development at ages 4 through 7 years. J Pediatr (1979) 1.08
Relationship of the human cumulus-free oocyte maturational profile with in vitro outcome parameters after intracytoplasmic sperm injection. J Assist Reprod Genet (1999) 1.02
Ethnicity, plasma phospholipid fatty acid composition and inflammatory/endothelial activation biomarkers in the Multi-Ethnic Study of Atherosclerosis (MESA). Eur J Clin Nutr (2012) 1.02
Maternal phenylketonuria. Detrimental effects on embryogenesis and fetal development. Am J Dis Child (1969) 1.02
Rabbit brain phosphofructokinase. Comparison of regulatory properties with those of other phosphofructokinase isozymes. J Biol Chem (1974) 1.01
Delayed pulmonary phosphatidylglycerol synthesis and reversal by prenatal dexamethasone in fetal rats of streptozotocin-diabetic mothers. Exp Lung Res (1983) 0.98
Short-term and long-term variability of plasma homocysteine measurement. Clin Chem (1997) 0.96
Distribution of phosphofructokinase isozymes in rabbit, mouse, guinea pig and rat. Comp Biochem Physiol B (1975) 0.93
Multiple hamartoma syndrome (Cowden disease). Arch Dermatol (1974) 0.93
Endocardial fibroelastosis occurring in a mother and son. Pediatrics (1966) 0.92
Phosphatidylglycerol in 261 samples of amniotic fluid from normal and diabetic pregnancies, as measured by one-dimensional thin-layer chromatography. Clin Chem (1979) 0.92
Detection of azoospermic factor genes in Chinese men with azoospermia or severe oligozoospermia. J Assist Reprod Genet (1999) 0.91
Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels. Clin Genet (2000) 0.91
Screening urine of 3-week-old newborns: transient methylmalonic and hydroxyphenyllactic aciduria. Biochem Med Metab Biol (1992) 0.90
Aspartyl residue 10 is essential for ATPase activity of rat hsc70. J Biol Chem (1993) 0.90
Perilipin polymorphism interacts with saturated fat and carbohydrates to modulate insulin resistance. Nutr Metab Cardiovasc Dis (2010) 0.89
Factor VII coagulant activity, factor VII -670A/C and -402G/A polymorphisms, and risk of venous thromboembolism. J Thromb Haemost (2007) 0.88
Relation of C-reactive protein and other cardiovascular risk factors to penile vascular disease in men with erectile dysfunction. Int J Impot Res (2003) 0.88
Effect of retinoic acid on implantation and post-implantation development of mouse embryos in vitro. Hum Reprod (2001) 0.88
Prospective study of the A455V polymorphism in the thrombomodulin gene, plasma thrombomodulin, and incidence of venous thromboembolism: the LITE Study. J Thromb Haemost (2003) 0.88
Clinical implications of intracytoplasmic sperm injection using cryopreserved testicular spermatozoa from men with azoospermia. J Reprod Med (2000) 0.87
Children with superior intelligence at 7 years of age: a prospective study of the influence of perinatal, medical, and socioeconomic factors. Am J Dis Child (1976) 0.87
Double-light phototherapy for neonatal hyperbilirubinemia. J Pediatr (1973) 0.86
The effect of antibiotics on the results of the Guthrie test given to phenylketonuric patients. J Pediatr (1968) 0.85
The shift of an increase in phosphofructokinase activity from protein synthesis-dependent to -independent mode during concanavalin A induced lymphocyte proliferation. Biochem Biophys Res Commun (1980) 0.85
Coping with aversive stimulation in the neonatal period: quiet sleep and plasma cortisol levels during recovery from circumcision. Child Dev (1985) 0.85
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network. Nutr Metab Cardiovasc Dis (2012) 0.85
Effects of fluvastatin (XU 62-320), an HMG-CoA reductase inhibitor, on the distribution and composition of low density lipoprotein subspecies in humans. Atherosclerosis (1991) 0.84
Maternal phenylketonuria-chronology of the detrimental effects on embryogenesis and fetal development: pathological report, survey, clinical application. Pediatr Pathol (1986) 0.84
Determination of the efficiency of controlled ovarian hyperstimulation in the gonadotropin-releasing hormone agonist-suppression cycle using the initial follicle count during gonadotropin stimulation. J Assist Reprod Genet (2001) 0.84
Simple and rapid method for extraction of DNA from fresh and cryopreserved clotted human blood. Clin Chem (1996) 0.84
Obesity modifies the association between plasma phospholipid polyunsaturated fatty acids and markers of inflammation: the Multi-Ethnic Study of Atherosclerosis. Int J Obes (Lond) (2011) 0.84
Improved thin-layer chromatography of disaturated phosphatidylcholine in amniotic fluid. Clin Chem (1981) 0.84
An adult phenylketonuric with schizophrenia. Clinical and biochemical similarities and possible genetic connection between the two diseases. Minn Med (1979) 0.84
Approaches to study interactions between kinesin motors and membranes. Methods Mol Biol (2001) 0.83
Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome. Pediatr Res (1989) 0.83
A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506). Arterioscler Thromb Vasc Biol (1997) 0.83
Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: a single nucleotide substitution in the second repeat prevents multiple alternate splicing. Am J Med Genet (2000) 0.83
Functional size of photosynthetic electron transport chain determined by radiation inactivation. Plant Physiol (1987) 0.83
Codon-54 polymorphism of the fatty acid-binding protein 2 gene is associated with elevation of fasting and postprandial triglyceride in type 2 diabetes. J Clin Endocrinol Metab (2000) 0.83
Identification and characterization of androgen receptor associated coregulators in prostate cancer cells. J Biol Regul Homeost Agents (2001) 0.83
Tripling of serum progesterone (P4) and embryonic morphological features in conception and nonconception cycles, after human in vitro fertilization. J In Vitro Fert Embryo Transf (1988) 0.82
Cloning and nucleotide sequencing of the second internal transcribed spacer of ribosomal DNA for three species of Eimeria from chickens in Taiwan. Vet J (2005) 0.82
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy. Heart (1997) 0.82
Endothelial nitric oxide gene polymorphism (Glu298Asp) is not associated with coronary artery disease in Turkish population. Thromb Haemost (2002) 0.82
ADAM17_i33708A>G polymorphism interacts with dietary n-6 polyunsaturated fatty acids to modulate obesity risk in the Genetics of Lipid Lowering Drugs and Diet Network study. Nutr Metab Cardiovasc Dis (2009) 0.81
School behavior profile ratings of phenylketonuric children. Am J Ment Defic (1968) 0.81
Amino acid abnormalities in infants with extrahepatic biliary atresia and cirrhosis. J Pediatr Gastroenterol Nutr (1988) 0.81
Prenatal and postnatal developmental consequences of maternal phenylketonuria. Pediatrics (1966) 0.81
Phenylketonuric patients decades after diet. J Inherit Metab Dis (1995) 0.81
Orthodontic correction of a mandibular first molar deeply impacted by an odontoma: a case report. Quintessence Int (1997) 0.81
Hybridization of rabbit muscle and liver phosphofructokinases. Arch Biochem Biophys (1972) 0.80
Clinical manifestations of mannosidosis--a longitudinal study. Am J Med (1976) 0.80
Effects of induction anesthetic agents on outcome of assisted reproductive technology: a comparison of propofol and thiopental sodium. Chang Gung Med J (2000) 0.80
Tensile bond strength of reused orthodontic metal brackets. Zhonghua Ya Yi Xue Hui Za Zhi (1991) 0.80
Children with phenylketonuria: the interface of family and child functioning. J Dev Behav Pediatr (1991) 0.80
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency. Am J Hum Genet (1995) 0.80
Growth and bone characteristics of phenylketonurics. Comparative analysis of treated and untreated phenylketonuric children. Am J Dis Child (1966) 0.80
Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantation. Birth Defects Orig Artic Ser (1986) 0.80
Changes in composition and distribution of LDL subspecies in hypertriglyceridemic and hypercholesterolemic patients during gemfibrozil therapy. Atherosclerosis (1994) 0.80
Norwegian scabies in Bloom's syndrome. Arch Dermatol (1979) 0.80
Effect of hypothermic pulmonary artery flushing on capillary filtration coefficient. Transplantation (2000) 0.80
Fetal rat lung phosphatidylcholine synthesis in diabetic and normal pregnancies: a comparison of prenatal dexamethasone treatments. Biochim Biophys Acta (1981) 0.79
Semen studies on phenylketonurics. Biochem Med (1981) 0.79
The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene. Nutr Metab Cardiovasc Dis (2009) 0.79
Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies. Int J Obes (Lond) (2013) 0.79
Cowden disease. Birth Defects Orig Artic Ser (1975) 0.79
Causes of death of institutionalized phenylketonuric (PKU) patients-A national survey. Minn Med (1976) 0.79
Psychiatric diagnosis and behavioral characteristics of phenylketonuric children. J Nerv Ment Dis (1986) 0.78
Comparable clinical outcomes of tubal embryo transfer for oligoastheno-teratozoospermia treated with intracytoplasmic sperm injection and for female infertility treated with in vitro fertilization. Chang Gung Med J (2000) 0.78
The effects of circumcision on serum cortisol and behavior. Psychoneuroendocrinology (1981) 0.78
Free amino acid analysis of untimed and 24-h urine samples compared. Clin Chem (1980) 0.78
Single-strand conformational polymorphisms (SSCP): studies of the genetic polymorphisms of exon 4 of apolipoprotein C III. Clin Biochem (1995) 0.78
Screening for urinary oligosaccharides and simple sugars by thin-layer chromatography. Med Lab Sci (1979) 0.78
Corpus luteum function during pregnancies of previously infertile women. Obstet Gynecol (1976) 0.78