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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)

TimeframeStudies, this research(%)All Research%
pre-199039 (97.50)18.7374
1990's1 (2.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bear, WD; Deshmukh, DS1
Dawson, G; Tsay, GC2
Beyreiss, K1
Borst, P; Hamers, MN; Molenaar, JL; Rietra, PJ; Tager, JM1
Brady, RO2
Callahan, JW; Pinsky, L; Wolfe, LS1
Harvey, J; Robertson, WV1
Brady, RO; de Webster, HF; Hogan, EL; Matthieu, JM; Quarles, RH1
Berra, B; Brunngraber, EG; Di Palma, S1
Wenger, DA1
Anderson, CF; DeWeed, JH; Frohnert, PP; Holley, KE; Kazmier, FJ; Riley, FC; Suros, J; Woods, JE1
Fishman, PH1
Greenfield, S; Morell, P; Norton, WT; Wisniewski, H1
Hill, HZ; Puck, TT1
Kitagawa, T1
Dahlqvist, A; Hultberg, B; Ockerman, PA1
Borst, P; Rietra, PJ; Tager, JM1
Clarke, JT; Perlin, AS; Wolfe, LS1
Li, SC; Li, YT1
Gregoire, PE; Jonniaux, G; Voet, W1
Montreuil, J; Strecker, G1
Galli, C; Kneebone, GM; Paoletti, R1
Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW1
Desnick, RJ; Krivit, W; Sweeley, CC1
Mandel, P; Neskovic, N; Nussbaum, JL1
Dawson, G; Stein, AO1
Griffin, CE; Snyder, PD; Sweeley, CC1
Clarke, JT; Crawhall, JC; Knaack, J; Wolfe, LS1
Bensaude, I; Callahan, J; Philippart, M1
Dawson, G; Matalon, R; Stein, AO1
O'Brien, JS; Okada, S1
Hooghwinkel, GJ; van Creveld, S1
Kaback, MM; Miller, K; Percy, AK; Sonneborn, M1
Batt, RD; Hocking, JD; Jolly, RD1
Bisson, PG; Caldwell, RA; Hall, GH; Shaldon, C1
Boisse, J1
O'Brien, JS; Okada, S; Veath, ML1
Duncan, C; Menkes, JH; Moossy, J1

Reviews

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

ArticleYear
[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

ArticleYear
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