galactose has been researched along with Lipid Metabolism, Inborn Error in 40 studies
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 | 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 |
5 review(s) available for galactose and Lipid Metabolism, Inborn Error
Article | Year |
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[Clinical and pathobiochemical findings in genetic diseases of carbohydrate and lipid metabolism].
Topics: Carbohydrate Metabolism, Inborn Errors; Fructose; Galactose; Glycogen Storage Disease; Humans; Hyperlipoproteinemias; Lipid Metabolism, Inborn Errors; Sphingolipidoses | 1992 |
Disorders of lipid metabolism.
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.
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].
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].
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 |
35 other study(ies) available for galactose and Lipid Metabolism, Inborn Error
Article | Year |
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The distribution and biosynthesis of the myelin-galactolipids in the subcellular fractions of brains of quaking and normal mice during development.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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].
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].
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 |