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galactose and Lipid Metabolism, Inborn Error

galactose has been researched along with Lipid Metabolism, Inborn Error in 40 studies

Research

Studies (40)

Timeframe	Studies, this research(%)	All Research%
pre-1990	39 (97.50)	18.7374
1990's	1 (2.50)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bear, WD; Deshmukh, DS	1
Dawson, G; Tsay, GC	2
Beyreiss, K	1
Borst, P; Hamers, MN; Molenaar, JL; Rietra, PJ; Tager, JM	1
Brady, RO	2
Callahan, JW; Pinsky, L; Wolfe, LS	1
Harvey, J; Robertson, WV	1
Brady, RO; de Webster, HF; Hogan, EL; Matthieu, JM; Quarles, RH	1
Berra, B; Brunngraber, EG; Di Palma, S	1
Wenger, DA	1
Anderson, CF; DeWeed, JH; Frohnert, PP; Holley, KE; Kazmier, FJ; Riley, FC; Suros, J; Woods, JE	1
Fishman, PH	1
Greenfield, S; Morell, P; Norton, WT; Wisniewski, H	1
Hill, HZ; Puck, TT	1
Kitagawa, T	1
Dahlqvist, A; Hultberg, B; Ockerman, PA	1
Borst, P; Rietra, PJ; Tager, JM	1
Clarke, JT; Perlin, AS; Wolfe, LS	1
Li, SC; Li, YT	1
Gregoire, PE; Jonniaux, G; Voet, W	1
Montreuil, J; Strecker, G	1
Galli, C; Kneebone, GM; Paoletti, R	1
Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW	1
Desnick, RJ; Krivit, W; Sweeley, CC	1
Mandel, P; Neskovic, N; Nussbaum, JL	1
Dawson, G; Stein, AO	1
Griffin, CE; Snyder, PD; Sweeley, CC	1
Clarke, JT; Crawhall, JC; Knaack, J; Wolfe, LS	1
Bensaude, I; Callahan, J; Philippart, M	1
Dawson, G; Matalon, R; Stein, AO	1
O'Brien, JS; Okada, S	1
Hooghwinkel, GJ; van Creveld, S	1
Kaback, MM; Miller, K; Percy, AK; Sonneborn, M	1
Batt, RD; Hocking, JD; Jolly, RD	1
Bisson, PG; Caldwell, RA; Hall, GH; Shaldon, C	1
Boisse, J	1
O'Brien, JS; Okada, S; Veath, ML	1
Duncan, C; Menkes, JH; Moossy, J	1

Reviews

5 review(s) available for galactose and Lipid Metabolism, Inborn Error

Article	Year
[Clinical and pathobiochemical findings in genetic diseases of carbohydrate and lipid metabolism]. Zentralblatt fur Pathologie, 1992, Volume: 138, Issue:3 Topics: Carbohydrate Metabolism, Inborn Errors; Fructose; Galactose; Glycogen Storage Disease; Humans; Hyperlipoproteinemias; Lipid Metabolism, Inborn Errors; Sphingolipidoses	1992
Disorders of lipid metabolism. Biochemical Society symposium, 1972, Issue:35 Topics: Adult; Animals; Bone Marrow; Cell Line; Ceramides; Child; Fabry Disease; Fucose; Galactose; Gangliosides; Gaucher Disease; Genetic Variation; Glycolipids; Glycoside Hydrolases; Humans; Leukemia, Myeloid; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipidoses; Mice; Niemann-Pick Diseases; Sulfoglycosphingolipids	1972
Normal and abnormal biosynthesis of gangliosides. Chemistry and physics of lipids, 1974, Volume: 13, Issue:4 Topics: Animals; Brain; Butyrates; Cell Membrane; Cell Transformation, Neoplastic; Cells, Cultured; Cholera; Galactosamine; Galactose; Gangliosides; HeLa Cells; Hexosyltransferases; Humans; Lipid Metabolism, Inborn Errors; Male; Mice; Oncogenic Viruses; Rats; Sialic Acids; Subcellular Fractions; Toxins, Biological; Transferases; Uridine Diphosphate Sugars	1974
[Congenital metabolic inborn errors, with the exception of amino acid metabolism]. Shinkei kenkyu no shimpo. Advances in neurological sciences, 1968, Volume: 12, Issue:1 Topics: Amino Acids; Carbohydrate Metabolism, Inborn Errors; Galactose; Humans; Hypercalcemia; Intellectual Disability; Kidney Function Tests; Lipid Metabolism, Inborn Errors; Metabolism, Inborn Errors; Metal Metabolism, Inborn Errors; Proline; Purine-Pyrimidine Metabolism, Inborn Errors; Renal Tubular Transport, Inborn Errors	1968
[New etiologic approach to periodic ketoacidosis in children]. Canadian Medical Association journal, 1971, Aug-07, Volume: 105, Issue:3 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Dehydration; Diabetic Ketoacidosis; Female; Glycogen Storage Disease; Hexoses; Humans; Hydrogen-Ion Concentration; Hypoglycemia; Infant; Infant, Newborn; Ketone Bodies; Lactation Disorders; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Methionine; Periodicity; Pregnancy; Propionates; Pyruvates; Vomiting	1971

Other Studies

35 other study(ies) available for galactose and Lipid Metabolism, Inborn Error

Article	Year
The distribution and biosynthesis of the myelin-galactolipids in the subcellular fractions of brains of quaking and normal mice during development. Journal of neurochemistry, 1977, Volume: 28, Issue:5 Topics: Animals; Brain; Cerebrosides; Female; Galactose; Glycolipids; Lipid Metabolism, Inborn Errors; Male; Mice; Microsomes; Myelin Sheath; Spinal Cord; Subcellular Fractions; Sulfoglycosphingolipids	1977
Structure of the glycopeptide storage material in GM 1 gangliosidosis. Sequence determination with specific endo- and exoglycosidases. Biochimica et biophysica acta, 1975, Apr-07, Volume: 385, Issue:2 Topics: Amino Acids; Chemical Phenomena; Chemistry; Escherichia coli; Galactose; Galactosidases; Gangliosides; Glycopeptides; Hexosamines; Humans; Lipid Metabolism, Inborn Errors; Liver; Plants; Trisaccharides	1975
Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolism. Biochemical and biophysical research communications, 1975, Apr-07, Volume: 63, Issue:3 Topics: alpha-L-Fucosidase; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Fucose; Galactose; Galactosidases; Glucosamine; Glycopeptides; Hexosaminidases; Humans; Lipid Metabolism, Inborn Errors; Mannose; Mannosidases; Metabolism, Inborn Errors; Sialic Acids; Skin	1975
Investigation of the alpha-galactosidase deficiency in Fabry's disease using antibodies against the purified enzyme. European journal of biochemistry, 1974, Jul-01, Volume: 46, Issue:1 Topics: Animals; Antibodies; Antibody Formation; Chemical Precipitation; Chromatography; Chromatography, Gel; Cross Reactions; Dialysis; Fabry Disease; Galactose; Galactosidases; Glycosides; Humans; Immune Tolerance; Immunoassay; Immunodiffusion; Immunoelectrophoresis; Isoenzymes; Kidney; Lipid Metabolism, Inborn Errors; Male; Nitrophenols; Rabbits; Ultrafiltration	1974
G M1 -gangliosidosis (Type II): studies on a fibroblast cell strain. Biochemical medicine, 1970, Volume: 4, Issue:3 Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Carbon Isotopes; Child, Preschool; Chromatography; Chromatography, Gel; Chromatography, Thin Layer; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glucosamine; Glycolipids; Glycosaminoglycans; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Skin	1970
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine. Biochemical medicine, 1972, Volume: 6, Issue:3 Topics: Achondroplasia; Adolescent; Adult; Aged; Aging; Arthritis, Rheumatoid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Colorimetry; Dermatomyositis; Female; Galactose; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Infant, Newborn; Intellectual Disability; Lipid Metabolism, Inborn Errors; Male; Methods; Middle Aged; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfuric Acids	1972
The adnormal biochemistry of inherited disorders of lipid metabolism. Federation proceedings, 1973, Volume: 32, Issue:6 Topics: Brain; Ceramides; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Female; Fibroblasts; Galactose; Galactosidases; Gaucher Disease; Glucose; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Humans; Intestines; Kidney; Leukocytes; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Muscles; Niemann-Pick Diseases; Phosphoric Diester Hydrolases; Sphingomyelins; Spleen; Sulfoglycosphingolipids; Syndrome	1973
Characterization of the fraction obtained from the CNS of Jimpy mice by a procedure for myelin isolation. Journal of neurochemistry, 1974, Volume: 23, Issue:3 Topics: Aging; Animals; Brain; Carbon Radioisotopes; Cell Fractionation; Cell Membrane; Cerebrosides; Chromatography, Thin Layer; Electrophoresis, Polyacrylamide Gel; Fucose; Galactose; Glycoproteins; Lipid Metabolism, Inborn Errors; Lipoproteins; Mice; Mice, Inbred Strains; Microscopy, Electron; Mutation; Myelin Sheath; Nerve Tissue Proteins; Nucleotides, Cyclic; Phosphoric Diester Hydrolases; Tritium	1974
Altered levels of tissue gangliosides and glycoproteins in the infantile form of GM1-gangliosidosis. Clinica chimica acta; international journal of clinical chemistry, 1974, Dec-17, Volume: 57, Issue:3 Topics: Brain; Cerebrosides; Chromatography, Thin Layer; Female; Fucose; Galactose; Galactosidases; Gangliosides; Glycoproteins; Hexosamines; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Liver; Lung; Male; Mannose; Phospholipids; Spleen; Sulfoglycosphingolipids	1974
Studies on galactosyl ceramide and lactosyl ceramide beta-galactosidase. Chemistry and physics of lipids, 1974, Volume: 13, Issue:4 Topics: Brain; Ceramides; Cerebrosides; Death, Sudden; Galactose; Galactosidases; Glycosides; Hot Temperature; Humans; Infant; Kinetics; Lactose; Leukodystrophy, Globoid Cell; Lipid Metabolism, Inborn Errors	1974
A kidney transplant patient with Fabry's disease. Unusual features. Archives of surgery (Chicago, Ill. : 1960), 1973, Volume: 106, Issue:2 Topics: Adult; Cadaver; Ceramides; Galactose; Galactosidases; Glycolipids; Heparin; Humans; Kidney Failure, Chronic; Kidney Transplantation; Leukocytes; Lipid Metabolism, Inborn Errors; Male; Pulmonary Embolism; Subclavian Vein; Syndrome; Thrombophlebitis; Transplantation, Homologous; Vena Cava, Inferior	1973
Isolation and characterization of myelin protein from adult quaking mice and its similarity to myelin protein of young normal mice. Advances in experimental medicine and biology, 1972, Volume: 32, Issue:0 Topics: Aging; Animals; Brain; Centrifugation, Density Gradient; Cerebrosides; Electrophoresis, Disc; Galactose; Hexosyltransferases; Homozygote; Lipid Metabolism, Inborn Errors; Lipoproteins; Mice; Microscopy, Electron; Mutation; Myelin Sheath; Nerve Tissue Proteins; Organ Size; Spinal Cord	1972
Detection of inborn errors of metabolism: galactosemia. Science (New York, N.Y.), 1973, Mar-16, Volume: 179, Issue:4078 Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carbon Dioxide; Carbon Isotopes; Cells, Cultured; Cystic Fibrosis; Female; Fibroblasts; Galactose; Galactosemias; Gangliosides; Humans; Infant; Kinetics; Lactones; Lipid Metabolism, Inborn Errors; Male; Pregnancy; Prenatal Diagnosis; Skin; Tritium	1973
Gargoylism: hydrolysis of beta-galactosides and tissure accumulation of galactose- and mannose-containing compounds. The Journal of clinical investigation, 1970, Volume: 49, Issue:2 Topics: Brain; Child; Chromatography; Chromatography, Gas; Galactose; Galactosidases; Glucose; Humans; Inositol; Lipid Metabolism, Inborn Errors; Liver; Mannose; Mucopolysaccharidoses	1970
Detection and properties of an acid -galactosidase (ceramidetrihexosidase) in normal human urine. Biochimica et biophysica acta, 1972, Oct-25, Volume: 279, Issue:3 Topics: Ammonium Sulfate; Ceramides; Cerebrosides; Chromatography, Thin Layer; Coumarins; Drug Stability; Freezing; Galactose; Galactosidases; Genotype; Glycolipids; Glycosides; Humans; Hydrogen-Ion Concentration; Inositol; Kinetics; Lipid Metabolism, Inborn Errors; Nitrobenzenes; Oligosaccharides	1972
Evidence for a terminal -D-galactopyranosyl residue in galactosylgalactosylglucosylceramide from human kidney. The Journal of biological chemistry, 1971, Sep-25, Volume: 246, Issue:18 Topics: Alcohol Oxidoreductases; Borohydrides; Brain Chemistry; Ceramides; Chemical Phenomena; Chemistry; Fatty Acids; Galactose; Galactosidases; Gangliosides; Glycolipids; Glycosides; Humans; Hydrogen-Ion Concentration; Hydrolysis; Isomerism; Kidney; Lipid Metabolism, Inborn Errors; Magnetic Resonance Spectroscopy; Methods; Oligosaccharides; Optical Rotation; Oxidation-Reduction; Pyridines; Sphingolipids; Temperature; Tritium	1971
Anomeric configuration of galactose residues in ceramide trihexosides. The Journal of biological chemistry, 1971, Jun-10, Volume: 246, Issue:11 Topics: Animals; Cerebrosides; Chromatography, Ion Exchange; Cricetinae; Erythrocytes; Fibroblasts; Galactose; Galactosidases; Glycolipids; Humans; Isomerism; Kidney; Kinetics; Lipid Metabolism, Inborn Errors; Mice; Plants; Sarcoma	1971
[Urinary glycolipids in Fabry's disease]. Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 33, Issue:2 Topics: Cerebrosides; Child; Chromatography; Chromatography, Gas; Chromatography, Ion Exchange; Chromatography, Paper; Chromatography, Thin Layer; Dialysis; Fatty Acids; Fatty Acids, Essential; Galactose; Glycolipids; Humans; Kidney; Lipid Metabolism, Inborn Errors; Liver; Palmitic Acids; Sphingosine; Sulfur	1971
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency]. Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 33, Issue:2 Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids	1971
An inborn error of cerebroside biosynthesis as the molecular defect of the Jimpy mouse brain. Life sciences, 1969, Sep-15, Volume: 8, Issue:18 Topics: Animals; Brain; Brain Chemistry; Carbon Isotopes; Cerebrosides; Galactose; Lipid Metabolism, Inborn Errors; Mice; Phospholipids	1969
Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis. Pediatric research, 1969, Volume: 3, Issue:6 Topics: Biopsy; Bone Marrow; Bone Marrow Cells; Brain; Culture Media; Culture Techniques; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glycolipids; Humans; Infant; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Niemann-Pick Diseases; Rheumatic Heart Disease; Skin	1969
A method for the quantitative determination of neutral glycosphingolipids in urine sediment. Journal of lipid research, 1970, Volume: 11, Issue:1 Topics: Adolescent; Adult; Angiokeratoma; Arthritis; Cerebrosides; Child; Child, Preschool; Chloroform; Chromatography, Gas; Chromatography, Thin Layer; Female; Galactose; Glucose; Glycosides; Heterozygote; Humans; Hydrogen-Ion Concentration; Lactose; Lipid Metabolism, Inborn Errors; Lipids; Male; Methanol; Methods; Middle Aged; Silicon	1970
A study of glycolipid metabolism in myelination disorder of Jimpy and Quaking mice. Brain research, 1970, Jun-30, Volume: 21, Issue:1 Topics: Amino Alcohols; Animals; Brain; Carbon Isotopes; Cerebrosides; Chromatography, Thin Layer; Demyelinating Diseases; Galactose; Gangliosides; Glycolipids; Glycols; Lipid Metabolism, Inborn Errors; Lipids; Mice; Microsomes; Mutation; Sulfates; Transferases	1970
Lactosyl ceramidosis: catabolic enzyme defect of glycosphingolipid metabolism. Science (New York, N.Y.), 1970, Oct-30, Volume: 170, Issue:3957 Topics: Bone Marrow; Bone Marrow Cells; Brain; Child, Preschool; Chromatography, Gas; Female; Galactose; Galactosidases; Glycolipids; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Tritium	1970
Chemistry of glycosphingolipids Fabry's disease. Chemistry and physics of lipids, 1970, Volume: 4, Issue:3 Topics: Adult; Amino Alcohols; Chemical Phenomena; Chemistry; Chromatography, Thin Layer; Disaccharides; Fatty Acids; Galactose; Glucose; Glycolipids; Glycols; Humans; Hydrolysis; Kidney; Lipid Metabolism, Inborn Errors; Magnetic Resonance Spectroscopy; Methylation; Oligosaccharides; Oxidation-Reduction; Sphingolipids	1970
Ceramide trihexosidosis (fabry's disease) without skin lesions. The New England journal of medicine, 1971, Feb-04, Volume: 284, Issue:5 Topics: Adult; Amino Alcohols; Biopsy; Chromatography, Thin Layer; Disaccharides; Fatty Acids; Galactose; Galactosidases; Glycolipids; Glycols; Hexoses; Humans; Hydrolases; Kidney; Lactose; Leukocytes; Lipid Metabolism, Inborn Errors; Lysosomes; Male; Microscopy, Electron; Middle Aged; Proteinuria	1971
Fabry's disease as an -galactosidosis: evidence for an -configuration in trihexosyl ceramide. Biochemical and biophysical research communications, 1971, May-21, Volume: 43, Issue:4 Topics: Animals; Bile Acids and Salts; Carbon Isotopes; Cerebrosides; Chemical Phenomena; Chemistry; Coffee; Culture Techniques; Disaccharides; Fibroblasts; Fruit; Galactose; Galactosidases; Glycolipids; Glycosides; Humans; Hydrogen-Ion Concentration; Intestine, Small; Lactose; Lipid Metabolism, Inborn Errors; Lymph Nodes; Nitrophenols; Plants; Polysaccharides; Rabbits; Rats; Skin; Stereoisomerism; Tritium	1971
Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts. The Journal of pediatrics, 1971, Volume: 79, Issue:3 Topics: Brain Diseases; Cerebrosides; Chromatography, Gas; Chromatography, Thin Layer; Culture Techniques; Fibroblasts; Galactose; Glycoside Hydrolases; Heterozygote; Lactose; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Sphingolipids	1971
Generalized gangliosidosis: beta-galactosidase deficiency. Science (New York, N.Y.), 1968, May-31, Volume: 160, Issue:3831 Topics: Acid Phosphatase; Aged; Brain; Carbon Isotopes; Child; Child, Preschool; Chromatography, Paper; Galactose; Galactosidases; Gangliosides; Glucosidases; Glycosides; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Middle Aged; Molecular Biology; Niemann-Pick Diseases; Nitrophenols; Spleen; Uracil Nucleotides	1968
Lipids in blood plasma and erythrocytes in juvenile amaurotic idiocy. Cholestyramine therapy. Archives of neurology, 1967, Volume: 17, Issue:3 Topics: Child; Cholesterol; Cholestyramine Resin; Erythrocytes; Hexosamines; Hexoses; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Neuraminic Acids; Phospholipids; Sphingomyelins	1967
Confirmatory studies in the prenatal diagnosis of sphingolipidoses. Pediatric research, 1973, Volume: 7, Issue:10 Topics: Abortion, Induced; Amniocentesis; Brain Chemistry; Female; Fetus; Galactosidases; Gangliosides; Hexosaminidases; Hexoses; Humans; Isoenzymes; Kidney; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Neuraminic Acids; Phenols; Pregnancy; Sphingolipidoses; Sphingolipids; Sulfoglycosphingolipids	1973
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease. The Biochemical journal, 1972, Volume: 128, Issue:1 Topics: Animals; Brain; Cattle; Cattle Diseases; Chick Embryo; Chromatography, Paper; Female; Glucosamine; Hexosaminidases; Hexoses; Lipid Metabolism, Inborn Errors; Liver; Lymph Nodes; Lysosomes; Male; Mannose	1972
Heparin-treated haemolytic-uraemic syndrome simulating Fabry's disease. British medical journal, 1971, May-08, Volume: 2, Issue:5757 Topics: Acute Kidney Injury; Anemia, Hemolytic; Child; Cholesterol; Chromatography, Thin Layer; Diagnosis, Differential; Glycolipids; Heparin; Hexoses; Humans; Kidney; Kidney Transplantation; Lipid Metabolism, Inborn Errors; Lipids; Male; Prednisone; Thrombocytopenia; Transplantation, Homologous	1971
Juvenile GM2 gangliosidosis: partial deficiency of hexosaminidase A. The Journal of pediatrics, 1970, Volume: 77, Issue:6 Topics: Amidohydrolases; Brain Diseases; Cerebral Cortex; Child, Preschool; Female; Gangliosides; Genes, Recessive; Hexoses; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Skin	1970
Molecular composition of the major glycolipids in globoid cell leukodystrophy. Neurology, 1966, Volume: 16, Issue:6 Topics: Brain Chemistry; Cerebral Cortex; Cerebrosides; Chromatography, Thin Layer; Demyelinating Diseases; Diffuse Cerebral Sclerosis of Schilder; Fatty Acids; Female; Glycolipids; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Sulfates	1966