Published in J Pediatr on May 01, 1981
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia. J Inherit Metab Dis (2001) 1.42
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency. J Clin Invest (1996) 1.18
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations. Am J Hum Genet (2000) 1.15
Isolated persistent hypermethioninemia. Am J Hum Genet (1995) 1.11
Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency. J Clin Invest (1988) 1.11
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. Am J Hum Genet (1997) 1.10
Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency. J Clin Invest (1995) 1.05
Insight into S-adenosylmethionine biosynthesis from the crystal structures of the human methionine adenosyltransferase catalytic and regulatory subunits. Biochem J (2013) 1.03
Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes. Orphanet J Rare Dis (2015) 1.01
One-carbon metabolism nutrient status and plasma S-adenosylmethionine concentrations in middle-aged and older Chinese in Singapore. Int J Mol Epidemiol Genet (2012) 0.96
Hepatic methionine adenosyltransferase deficiency in a 31-year-old man. Am J Hum Genet (1987) 0.93
Biochemistry and pharmacology of S-adenosyl-L-methionine and rationale for its use in liver disease. Drugs (1990) 0.93
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnancies. J Inherit Metab Dis (2003) 0.76
Crystallography captures catalytic steps in human methionine adenosyltransferase enzymes. Proc Natl Acad Sci U S A (2016) 0.75
Confirmation that MAT1A p.Ala259Val mutation causes autosomal dominant hypermethioninemia. Mol Genet Metab Rep (2017) 0.75
Antibodies to ribosomes in chronic active hepatitis. Gastroenterology (1979) 12.78
Hybrid plasmids containing an active thymidine kinase gene of Herpes simplex virus 1. Nucleic Acids Res (1979) 5.55
Comfrey herb tea-induced hepatic veno-occlusive disease. Am J Med (1989) 2.09
The ultrastructure of acidophilic "Councilman-like" bodies in the liver. Am J Pathol (1966) 2.04
Hepatitis after exposure to halothane. Ann Intern Med (1969) 1.95
The histological features of chronic hepatitis C and autoimmune chronic hepatitis: a comparative analysis. Hepatology (1992) 1.85
Serum bilirubin: a prognostic factor in primary biliary cirrhosis. Gut (1979) 1.78
A monoclonal antibody to a differentiation antigen present on mature human macrophages and absent from monocytes. J Immunol (1985) 1.76
Milk protein quantity and quality in low-birthweight infants: I. Metabolic responses and effects on growth. Pediatrics (1976) 1.70
Electron microscopy and immunoelectronmicroscopy of cytoplasmic hepatitis B antigen in hepatocytes. Am J Pathol (1974) 1.70
Fatty liver hepatitis and cirrhosis in obese patients. Am J Med (1979) 1.66
Antimitochondrial antibodies in jaundice following drug administration. JAMA (1969) 1.61
A cysteine-rich collagenous protein from bovine placenta. Isolation of its constituent polypeptide chains and some properties of the non-denatured protein. Eur J Biochem (1981) 1.56
Fat-storing cells (lipocytes) in human liver. Arch Pathol (1966) 1.55
Evaluation of colchicine therapy in primary biliary cirrhosis. Gastroenterology (1988) 1.55
Cholestasis is the result of hypoactive hypertrophic smooth endoplasmic reticulum in the hepatocyte. Lancet (1969) 1.54
Paradoxical elevation of serum cholesterol by clofibrate in patients with primary biliary cirrhosis. Gastroenterology (1969) 1.49
Immune processes in the pathogenesis of liver disease. Ann N Y Acad Sci (1965) 1.46
Antibodies to cytoplasmic antigens in primary biliary cirrhosis and chronic active hepatitis. J Lab Clin Med (1967) 1.46
Glutaric aciduria type II: report on a previously undescribed metabolic disorder. Clin Chim Acta (1976) 1.44
Lymphocyte stimulation and chronic liver disease. Lancet (1967) 1.42
HLA-DR expression in bile duct damage in hepatitis C. Mod Pathol (1993) 1.42
The histologic effects of low-dose methotrexate therapy for primary biliary cirrhosis. Arch Pathol Lab Med (1998) 1.42
Continuing changing patterns of disease in pyogenic liver abscess: a study of 38 patients. Am J Gastroenterol (1984) 1.40
Metabolism of L- 35 S-methionine in vitamin B 6 deficiency: observations on cystathioninuria. Biochem Med (1970) 1.40
Effect of weight reduction on hepatic abnormalities in overweight patients. Gastroenterology (1990) 1.40
Introduction and control of three invasive mosquito species in the Netherlands, July-October 2010. Euro Surveill (2010) 1.40
Pathophysiology of cholestasis. Hum Pathol (1970) 1.39
Introduction and establishment of the exotic mosquito species Aedes japonicus japonicus (Diptera: Culicidae) in Belgium. J Med Entomol (2009) 1.38
Mechanism of cholestasis. 6. Bile acids in human livers with or without biliary obstruction. Gastroenterology (1972) 1.34
Hepatic drug reactions. Prog Liver Dis (1972) 1.33
Nonsuppurative destructive chronic cholangitis and chronic hepatitis. Prog Liver Dis (1970) 1.28
D.N.A. polymerase in preparations containing Australia antigen. Lancet (1971) 1.27
Taurine: biological update. Annu Rev Biochem (1986) 1.27
The vocabulary of chronic hepatitis. N Engl J Med (1971) 1.26
Red cell transketolase as an indicator of nutritional deficiency. Am J Clin Nutr (1980) 1.26
Hepatocellular hyalin in cholestasis and cirrhosis: its diagnostic significance. Gastroenterology (1973) 1.23
Bridging the gap: an integrated paediatric to adult clinical service for young adults with kidney failure. BMJ (2012) 1.21
Tissue factor and cell signalling in cancer progression and thrombosis. J Thromb Haemost (2011) 1.20
The effect of altered thyroid function on the ultrastructure of the human liver. Am J Med (1971) 1.18
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997. Eur J Pediatr (1999) 1.17
Pyridoxine-dependency in homocystinuria. Lancet (1968) 1.16
A case of autochthonous Plasmodium vivax malaria, Corsica, August 2006. Euro Surveill (2006) 1.16
Bile ductules in cholestasis: morphologic evidence for secretion and absorption in man. Lab Invest (1967) 1.16
Evaluation of matrix-assisted laser desorption/ionization time of flight mass spectrometry for characterization of Culicoides nubeculosus biting midges. Med Vet Entomol (2010) 1.15
Methionine intolerance: a possible risk factor for coronary artery disease. J Am Coll Cardiol (1985) 1.14
Chronic passive congestion of the liver in man. Electron microscopic study of cell atrophy and intralobular fibrosis. Am J Pathol (1967) 1.13
Ultrastructural features in galactosamine-induced hepatitis. Exp Mol Pathol (1970) 1.12
Milk protein quantity and quality in low-birth-weight infants. III. Effects on sulfur amino acids in plasma and urine. J Pediatr (1977) 1.12
Intermittent cerebellar ataxia associated with hyperpyruvic acidemia, hyperalaninemia, and hyperalaninuria. Pediatrics (1969) 1.11
Chronic cholestasis in hepatic sarcoidosis with clinical features resembling primary biliary cirrhosis. Report of two cases. Am J Med (1987) 1.11
Nonalcoholic fatty liver disease. Prog Liver Dis (1986) 1.11
Homocystinuria due to cystathionine synthase deficiency: enzymatic and ultrastructural studies. J Pediatr (1974) 1.10
Expression of HLA class I antigens on hepatocytes in liver disease. Am J Pathol (1986) 1.10
Malignancy in primary biliary cirrhosis. High incidence of breast cancer in affected women. Am J Med (1984) 1.08
Structure of rat lung after protracted oxygen breathing. Arch Pathol (1967) 1.07
Primary biliary cirrhosis. Clin Gastroenterol (1975) 1.07
Microsomal metabolism of dimethylnitrosamine and the cytochrome P-450 dependency of its activation to a mutagen. Cancer Res (1973) 1.07
Bionomics of the established exotic mosquito species Aedes koreicus in Belgium, Europe. J Med Entomol (2012) 1.07
Metabolic correlates of eating behavior in severe obesity. Int J Obes Relat Metab Disord (2001) 1.06
Mechanism of cholestasis. 5. Bile acids in normal rat livers and in those after bile duct ligation. Gastroenterology (1972) 1.06
Respiratory impairment induced by smoking in children in secondary schools. Br Med J (Clin Res Ed) (1984) 1.06
Mediastinal tumors: biopsy under US guidance. Radiology (1989) 1.05
Factors influencing survival in pediatric acute leukemia. The SWCCSG experience, 1958-1970. Cancer (1973) 1.05
Wernicke's encephalopathy and hyperalimentation. JAMA (1978) 1.04
Morphologic changes in hamster liver during intrahepatic cholestasis induced by taurolithocholate. Lab Invest (1966) 1.04
Hepatocellular adaptation and injury. Structural and biochemical changes following dieldrin and methyl butter yellow. Lab Invest (1969) 1.03
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin. Eur J Pediatr (1984) 1.02
Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia. Science (1974) 1.02
Alpha-ketoadipic aciduria: degradation studies with fibroblasts,. Clin Chim Acta (1975) 1.02
Expression of cytokeratins in normal and diseased livers and in primary liver carcinomas. Arch Pathol Lab Med (1989) 1.01
Increased serum thyroid hormone binding and decreased free hormone in chronic active liver disease. N Engl J Med (1978) 1.01
Ornithine carbamoyltransferase deficiency in an adult male patient: significance of hepatic ultrastructure in clinical diagnosis. Pediatrics (1983) 1.01
Changes in hepatic structure in rats produced by breathing pure oxygen. J Cell Biol (1965) 1.01
Localization and organization of tRNA genes on the mitochondrial genomes of fertile and male sterile lines of maize. Mol Gen Genet (1990) 1.00
Mechanism of cholestasis. 4. Structural and biochemical changes in the liver and serum in rats after bile duct ligation. Gastroenterology (1971) 1.00
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets. Arch Dermatol (1994) 1.00
Sequence analysis of the tRNA(Tyr) and tRNA(Lys) genes and evidence for the transcription of a chloroplast-like tRNA(Met) in maize mitochondria. Curr Genet (1989) 1.00
Clinical-pathologic relations in primary biliary cirrhosis. Prog Liver Dis (1982) 0.99
Extrahepatic malignancy in chronic liver disease: report of six cases. Gastroenterology (1976) 0.99
Differential pattern of DNA-aneuploidy in human malignancies. Pathol Res Pract (1985) 0.99
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies. Clin Chim Acta (1975) 0.99
Benign giant lymphoid hyperplasia of the mediastinum with associated abnormalities of the immune system. J Pediatr (1974) 0.99
Dietary restriction of maternal lactose intake does not prevent accumulation of galactitol in the amniotic fluid of fetuses affected with galactosaemia. Prenat Diagn (1988) 0.98
Population dynamics of pest mosquitoes and potential malaria and West Nile virus vectors in relation to climatic factors and human activities in the Camargue, France. Med Vet Entomol (2007) 0.98
Excessive weight gain after liver transplantation. Transplantation (1991) 0.98
Body fat topography as an independent predictor of fatty liver. Metabolism (1993) 0.98
The liver in the acquired immunodeficiency syndrome: a clinical and histologic study. Hepatology (1985) 0.98
Fetal tissue amino acid concentrations in argininosuccinic aciduria and in "maternal homocystinuria". Clin Chim Acta (1979) 0.98
Glutaric aciduria type II: multiple defects in isolated muscle mitochondria and deficient beta-oxidation in fibroblasts. J Inherit Metab Dis (1984) 0.98
Hypertrophic, hypoactive smooth endoplasmic reticulum: a sensitive indicator of hepatotoxicity exemplified by dieldrin. Science (1968) 0.97
A procedure for the quantitative analysis of the sulphur amino acids of rat tissues. Biochem J (1967) 0.96
Budd-Chiari syndrome caused by a web in the inferior vena cava. Am J Med (1967) 0.95
In situ characterization of the cell-surface antigens of the mononuclear cell infiltrate and bile duct epithelium in primary biliary cirrhosis. Clin Immunol Immunopathol (1986) 0.95
Hereditary hyperphosphatasia. Studies of three siblings. Am J Med (1969) 0.95
Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome. Clin Chim Acta (1987) 0.95