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galactose and Lipidoses

galactose has been researched along with Lipidoses in 48 studies

Research

Studies (48)

TimeframeStudies, this research(%)All Research%
pre-199048 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
GIELEN, W; KLENK, E; LIEDTKE, U1
Ng Kin Kin, NM; Wolfe, LS1
Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI1
Cocquyt, G; Dacremont, G; Kint, JA1
Debuch, H; Gielen, W; Kannan, R; Kerènyi, L1
Brady, RO3
Suzuki, K1
Brown, B; Brunngraber, EG; Haberland, C; Witting, LA1
Kawamura, N; Taketomi, T1
McGuire, EJ; Roseman, S; Schachter, H1
Hiatt, W; Sattler, M; Wenger, DA1
Dastugue, G; Motta, C; Viallard, JL1
Dulaney, JT; Moser, HW; Sugita, M1
Makita, A; Takahashi, W; Yokoyama, T1
Aro, A; Brown, BD; Brunngraber, EG1
Fletcher, TF; Kurtz, HJ1
Yip, MC1
Montreuil, J; Strecker, G1
Tamai, Y; Yamakawa, T1
Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW1
Den, H; Kaufman, B; Roseman, S1
Dawson, G; Stein, AO1
Brady, RO; Kolodny, EH1
Dawson, G; Matalon, R; Stein, AO1
Kolodny, EH; Stone, AL1
Martensson, E; Stoffyn, A; Stoffyn, P1
O'Brien, JS; Okada, S1
Kennaway, NG; Woolf, LI1
Dain, JA; Yip, MC2
Krivit, W; Sweeley, CC; Vance, DE1
Wagner, A1
EDGAR, GW1
BRANTE, G1
Hooghwinkel, GJ; van Creveld, S1
Kaback, MM; Miller, K; Percy, AK; Sonneborn, M1
Brown, BD; Brunngraber, EG; Hof, H1
Minami, R; Nakao, T; Orii, T; Sukegawa, K1
Adelman, LS; Bass, NH; Young, E1
Debuch, H; Kannan, R; Tjiong, HB; Wiedemann, HR1
Booth, DA; Cumings, JN; Goodwin, H1
Borri, PF; Hooghwinkel, GJ1
Harzer, K; Jatzkewitz, H; Sandhoff, K; Wässle, W1
Bartsch, GG1
O'Brien, JS; Okada, S; Veath, ML1
Adachi, M; Friedland, J; Schneck, L; Valenti, C; Volk, BW1

Reviews

2 review(s) available for galactose and Lipidoses

ArticleYear
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
    Advances in experimental medicine and biology, 1976, Volume: 68

    Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses

1976
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

Other Studies

46 other study(ies) available for galactose and Lipidoses

ArticleYear
[BRAIN GANGLIOSIDES IN INFANTILE AMAUROTIC IDIOCY OF THE TAY-SACHS TYPE].
    Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1963, Volume: 334

    Topics: Brain; Chromatography; Fatty Acids; Galactose; Gangliosides; Glucose; Humans; Intellectual Disability; Lipidoses; Tay-Sachs Disease

1963
Storage and excretion of oligosaccharides and glycopeptides in the gangliosidoses.
    Advances in experimental medicine and biology, 1976, Volume: 68

    Topics: Galactose; Gangliosidoses; Glucosamine; Glycopeptides; Humans; Infant; Lipidoses; Liver; Mannose; Molecular Conformation; Molecular Weight; Oligosaccharides

1976
Brain sphingolipids in I cell disease (mucolipidosis II).
    Journal of neurochemistry, 1974, Volume: 22, Issue:4

    Topics: Abnormalities, Multiple; Ceramides; Cerebrosides; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Cytoplasmic Granules; Fibroblasts; Galactose; Gangliosides; Glucose; Humans; Lactose; Lipidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Neuraminic Acids; Retinitis Pigmentosa; Sphingolipids; Sphingomyelins; Sulfoglycosphingolipids; Syndrome

1974
[A sphingolipidosis with the accumulation of neutral glycosphingolipids, AO2(GM3) and A1(GM2)-ganglioside (author's transl)].
    Zeitschrift fur klinische Chemie und klinische Biochemie, 1974, Volume: 12, Issue:11

    Topics: Brain; Ceramides; Cerebellum; Cerebral Cortex; Child; Fatty Acids; Galactose; Gangliosides; Glucose; Glycolipids; Hexoses; Humans; Lipidoses; Palmitic Acids; Parietal Lobe; Pons; Putamen; Sphingolipidoses; Sphingolipids; Stearic Acids; Thalamus

1974
Cerebral GM1-gangliosidosis: chemical pathology of visceral organs.
    Science (New York, N.Y.), 1968, Mar-29, Volume: 159, Issue:3822

    Topics: Brain Diseases; Chromatography, Thin Layer; Galactose; Gangliosides; Glycosaminoglycans; Hexosamines; Humans; Lipidoses; Liver; Polysaccharides; Spleen

1968
Glycoproteins in Tay-sachs disease: isolation and carbohydrate composition of glycopeptides.
    Brain research, 1972, Mar-10, Volume: 38, Issue:1

    Topics: Brain; Brain Stem; Cerebellum; Cerebral Cortex; Child; Chromatography, Paper; Electrophoresis; Female; Galactose; Gangliosides; Glucose; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosaminidases; Humans; Infant; Lipidoses; Mannose; Peptides

1972
Cerebral and visceral glycolipids in a case of Tay-Sachs disease.
    Journal of biochemistry, 1969, Volume: 66, Issue:2

    Topics: Brain Chemistry; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Galactose; Glucose; Glycolipids; Hexoses; Humans; Infrared Rays; Kidney; Lipidoses; Liver; Silicon Dioxide; Spectrophotometry; Spleen; Time Factors

1969
Sialic acids. 13. A uridine diphosphate D-galactose: mucin galactosyltransferase from porcine submaxillary gland.
    The Journal of biological chemistry, 1971, Sep-10, Volume: 246, Issue:17

    Topics: Acetates; Animals; Cadmium; Calcium Chloride; Carbon Isotopes; Chlorides; Chromatography, Paper; Clostridium perfringens; Enzyme Activation; Galactosamine; Galactose; Galactosidases; Gangliosides; Glucosamine; Glucose; Glycoproteins; Hexosaminidases; Hexosyltransferases; Hydrogen-Ion Concentration; Kinetics; Lipidoses; Manganese; Mathematics; Models, Structural; Mucins; Neuraminic Acids; Neuraminidase; Nucleoside Diphosphate Sugars; Oligosaccharides; Ovalbumin; Sheep; Submandibular Gland; Surface-Active Agents; Swine; Uracil Nucleotides; Zinc

1971
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
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.
    Proceedings of the National Academy of Sciences of the United States of America, 1974, Volume: 71, Issue:3

    Topics: Adult; Brain; Ceramides; Female; Galactose; Galactosidases; Gangliosides; Humans; Infant; Lactose; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Liver; Male; Niemann-Pick Diseases; Skin; Spleen; Syndrome

1974
[Human cerebrospinal fluid hexosaminidases. Activity on N-acetyl-beta-D-glucosaminidic and N-acetyl-beta-galactosaminidic derivatives of 4-methyl-umbelliferone. Evaluation of A and B forms by their thermostability difference].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1972, Volume: 166, Issue:12

    Topics: Amidines; Cerebrospinal Fluid; Coumarins; Galactose; Glucose; Hexosaminidases; Humans; Lipidoses; Lysosomes

1972
Ceramidase deficiency in Farber's disease (lipogranulomatosis).
    Science (New York, N.Y.), 1972, Dec-08, Volume: 178, Issue:4065

    Topics: Acid Phosphatase; Adult; Carbon Isotopes; Ceramides; Cerebellum; Cerebrosides; Child; Child, Preschool; Congenital Abnormalities; Female; Galactose; Galactosidases; Glucose; Glycoside Hydrolases; Heart Defects, Congenital; Hexosaminidases; Humans; Hydrolases; Infant; Infant, Newborn; Intellectual Disability; Kidney; Lipidoses; Liver Cirrhosis, Biliary; Male; Metabolism, Inborn Errors; Neuraminidase; Pigmentation Disorders; Respiratory Distress Syndrome, Newborn

1972
Enzymatic degradation of Forssman hapten: a reinvestigation of the chemical structure.
    Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1973, Volume: 354, Issue:9

    Topics: Animals; Ceramides; Chromatography, Gas; Chromatography, Thin Layer; Forssman Antigen; Galactosamine; Galactose; Glucose; Glycolipids; Hexosaminidases; Horses; Humans; Immunoglobulin M; Kidney; Kinetics; Lipidoses; Mollusca

1973
Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis.
    Journal of neurochemistry, 1974, Volume: 22, Issue:1

    Topics: Acetamides; Brain; Brain Chemistry; Child, Preschool; Chromatography, Gel; Electrophoresis; Female; Fucose; Galactose; Gangliosides; Glucosamine; Glycoproteins; Hexosamines; Hexosaminidases; Humans; Lipidoses; Male; Mannose; Neuraminic Acids

1974
Animal model: globoid cell leukodystrophy in the dog.
    The American journal of pathology, 1972, Volume: 66, Issue:2

    Topics: Animals; Brain; Cerebrosides; Child; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; Disease Models, Animal; Dogs; Galactose; Galactosidases; Glycoside Hydrolases; Humans; Lipidoses; Macrophages

1972
The enzymic synthesis of gangliosides: uridine diphosphate galactose: N-acetylgalactosaminyl-(N-acetylneuraminyl)-galactosyl-glucosyl-ceramide galactosyltransferase in rat tissues.
    Biochimica et biophysica acta, 1972, Jul-19, Volume: 273, Issue:2

    Topics: Age Factors; Animals; Brain; Carbon Isotopes; Chromatography; Chromatography, Thin Layer; Digestive System; Female; Galactose; Gangliosides; Hexosyltransferases; Humans; Kidney; Lipidoses; Liver; Lung; Mammary Glands, Animal; Manganese; Muscles; Myocardium; Rats; Spleen; Uridine Diphosphate Sugars

1972
[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
Study on glucocerebroside in Tay-Sachs brain.
    The Japanese journal of experimental medicine, 1969, Volume: 39, Issue:1

    Topics: Brain Chemistry; Cerebrosides; Chromatography; Fatty Acids; Galactose; Gangliosides; Glucose; Humans; Infant; Infrared Rays; Lipidoses; Lipids; Spectrophotometry

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
Properties of some glycosyltransferases in embryonic chicken brain.
    The Journal of biological chemistry, 1970, Dec-25, Volume: 245, Issue:24

    Topics: Aging; Albumins; Amniotic Fluid; Animals; Brain; Carbon Isotopes; Chick Embryo; Cytosine Nucleotides; Detergents; Galactose; Gangliosides; Glucosamine; Glycoproteins; Guinea Pigs; Humans; Lipidoses; Mucins; Neuraminic Acids; Neuraminidase; Oligosaccharides; Serine; Transferases; Uracil Nucleotides; Vitreous Body; Xylose

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
Further studies on the elucidation of the enzymatic defect in Tay-Sachs disease.
    Neurology, 1970, Volume: 20, Issue:4

    Topics: Freezing; Galactose; Gangliosides; Glycoside Hydrolases; Hexosamines; Humans; Lipidoses; Muscles

1970
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
Circular dichroism of gangliosides from normal and Tay-Sachs tissues.
    Chemistry and physics of lipids, 1971, Volume: 6, Issue:3

    Topics: Amino Alcohols; Amino Sugars; Animals; Brain; Brain Chemistry; Cattle; Chemical Phenomena; Chemistry; Circular Dichroism; Cytosine Nucleotides; Fatty Acids; Galactose; Gangliosides; Glucose; Glycols; Hexosamines; Humans; Ketones; Lipidoses; Neuraminic Acids; Rats; Spleen; Transferases; Ultraviolet Rays

1971
Structure of kidney ceramide dihexoside sulfate.
    Biochimica et biophysica acta, 1968, Mar-04, Volume: 152, Issue:2

    Topics: Cerebrosides; Chemical Phenomena; Chemistry; Chromatography, Thin Layer; Galactose; Hexoses; Humans; Kidney; Lipidoses; Methylation; Sulfates

1968
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
Splenic lipids in Gaucher's disease.
    Journal of lipid research, 1968, Volume: 9, Issue:6

    Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism; Cerebrosides; Child; Child, Preschool; Chromatography; Chromatography, Thin Layer; Colorimetry; Freezing; Galactose; Gaucher Disease; Glucose; Glycolipids; Glycosides; Humans; Infant; Lipid Metabolism; Lipidoses; Methods; Middle Aged; Preservation, Biological; Spleen

1968
The inhibition of galactose oxidase.
    Enzymologia, 1968, Dec-31, Volume: 35, Issue:6

    Topics: Alcohol Oxidoreductases; Animals; Basidiomycota; Brain; Cattle; Copper; Galactose; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Molecular Weight; Osmotic Pressure

1968
Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis.
    Journal of lipid research, 1969, Volume: 10, Issue:2

    Topics: Adolescent; Adult; Cerebrosides; Child; Erythrocytes; Female; Galactose; Gaucher Disease; Glucose; Heterozygote; Humans; Lactose; Lipidoses; Male; Middle Aged

1969
The enzymic synthesis of ganglioside. 1. Brain uridine diphosphate D-galactose: N-acetyl-galactosaminyl-galactosyl-glucosyl-ceramide galactosyl transferase.
    Lipids, 1969, Volume: 4, Issue:4

    Topics: Age Factors; Amino Alcohols; Animals; Anura; Brain; Carbon Isotopes; Centrifugation; Chromatography, Thin Layer; Detergents; Fatty Acids; Galactose; Gangliosides; Glycolipids; Humans; Hydrogen-Ion Concentration; Intestine, Small; Kidney; Kinetics; Lipidoses; Liver; Microscopy, Electron; Models, Biological; Rats; Solubility; Transferases; Uracil Nucleotides

1969
[Concerning brain gangliosides in Tay-Sachs disease].
    Klinische Wochenschrift, 1966, Apr-01, Volume: 44, Issue:7

    Topics: Brain Chemistry; Child; Chromatography, Thin Layer; Galactose; Gangliosides; Glucose; Hexosamines; Humans; Lipidoses; Neuraminic Acids; Sphingomyelins; Stearic Acids

1966
[Biochemical approach to types of lipoidosis and leukodystrophy].
    Revue neurologique, 1955, Volume: 92, Issue:4

    Topics: Brain; Brain Diseases; Hexoses; Humans; Lipid Metabolism; Lipidoses; Lysosomal Storage Diseases; Phospholipids

1955
Studies on lipids in morbus Gaucher. I. Qualitative and quantitative determination of the hexose components in normal and Gaucher glycolipids.
    Acta Societatis Medicorum Upsaliensis, 1951, Sep-29, Volume: 56, Issue:3-4

    Topics: Glycolipids; Hexoses; Humans; Lipidoses; Lipids

1951
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
Determination of gangliosides, glycoproteins, and glycosaminoglycans in brain tissue.
    Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 32, Issue:2

    Topics: Acetates; Adult; Animals; Brain Chemistry; Brain Diseases; Cattle; Cerebral Cortex; Chemical Precipitation; Child; Child, Preschool; Chloroform; Chromatography, Gel; Dialysis; Electrophoresis; Fucose; Galactosemias; Gangliosides; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosamines; Hexoses; Humans; Hydrogen-Ion Concentration; Lipidoses; Methanol; Methods; Myelin Sheath; Neuraminic Acids; Papain; Peptide Hydrolases; Pyridinium Compounds; Rats; Solubility; Subacute Sclerosing Panencephalitis; Temperature

1971
Hyperglycopeptiduria in genetic mucolipidoses.
    The Tohoku journal of experimental medicine, 1974, Volume: 112, Issue:4

    Topics: Child; Child, Preschool; Chromatography, Paper; Female; Gangliosides; Gaucher Disease; Glycopeptides; Glycosaminoglycans; Hexoses; Humans; Infant; Lipidoses; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Neuraminic Acids; Sphingolipids; Sulfates; Uronic Acids

1974
Abnormal accumulation of sialoglycoproteins in a case of late infantile amaurotic idiocy.
    Neurology, 1974, Volume: 24, Issue:11

    Topics: Cerebral Cortex; Child, Preschool; Cholesterol; Gangliosides; Glycoproteins; Hexoses; Histocytochemistry; Humans; Inclusion Bodies; Lipid Metabolism; Lipidoses; Male; Microscopy, Electron; Neurons; Pigments, Biological; Sialic Acids

1974
Unusual glycolipids in brain cortex of a visceral lipidosis (Niemann-Pick disease?).
    Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 1974, Volume: 355, Issue:5

    Topics: Brain Chemistry; Ceramides; Cerebral Cortex; Cerebrosides; Child; Cholesterol; Chromatography; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Gangliosides; Glycolipids; Hexoses; Humans; Lipidoses; Lipids; Male; Niemann-Pick Diseases; Sulfoglycosphingolipids

1974
Abnormal gangliosides in Tay-Sachs disease, Niemann-Pick's disease, and gargoylism.
    Journal of lipid research, 1966, Volume: 7, Issue:3

    Topics: Amino Alcohols; Brain Chemistry; Cerebral Cortex; Chromatography, Thin Layer; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Mucopolysaccharidoses; Neuraminic Acids; Niemann-Pick Diseases; Sphingomyelins

1966
Comparative studies of glycolipids and carbohydrate moieties in brain and visceral organs in amaurotic idiocy and gargolylism.
    Pathologia Europaea, 1968, Volume: 3, Issue:2

    Topics: Adolescent; Adult; Aged; Brain Chemistry; Carbohydrate Metabolism; Child; Child, Preschool; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Liver; Middle Aged; Mucopolysaccharidoses; Neuraminic Acids; Spleen

1968
Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.
    Journal of neurochemistry, 1971, Volume: 18, Issue:12

    Topics: Brain; Brain Chemistry; Ceramides; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Galactosamine; Gangliosides; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Hexoses; Hot Temperature; Humans; Hydrogen-Ion Concentration; Infant; Isoelectric Focusing; Kidney; Lipid Metabolism; Lipidoses; Liver

1971
Glycolipid abnormalities in a myoclonic variant of late infantile amaurotic idiocy.
    Journal of lipid research, 1970, Volume: 11, Issue:3

    Topics: Brain; Carbohydrates; Cerebrosides; Child; Chromatography, Thin Layer; Gangliosides; Glycolipids; Hexoses; Humans; Lipidoses; Male

1970
Metabolic disorders of sphingolipid metabolism in man.
    Chemistry and physics of lipids, 1970, Volume: 5, Issue:1

    Topics: Amino Alcohols; Carbon Isotopes; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Esterases; Fatty Acids; Gangliosides; Gaucher Disease; Glycols; Hexoses; Humans; Lipid Metabolism; Lipidoses; Niemann-Pick Diseases; Sphingomyelins; Sulfuric Acids

1970
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
Early evolution of cytoplasmic inclusion bodies in Tay-Sachs disease.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1970, Volume: 135, Issue:3

    Topics: Amidines; Amidohydrolases; Brain; Chromatography; Electrophoresis; Embryo, Mammalian; Fetus; Gangliosides; Hexoses; Humans; Inclusion Bodies, Viral; Infant; Lipidoses; Liver; Microscopy, Electron

1970
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