Page last updated: 2024-08-22

mannose and Mucopolysaccharidoses

mannose has been researched along with Mucopolysaccharidoses in 19 studies

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-199019 (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
Yamashita, K1
Dawson, G; Matalon, R; Tsay, GC1
Elleder, M1
Ockerman, PA2
Autio, S; Berg, B; Hultberg, B; Ockerman, PA1
Lundblad, A; Masson, PK1
Van Hoof, F1
Eriksson, O; Hultberg, B; Ockerman, PA1
Spranger, JW; Wiedemann, HR2
Bain, AD; Butterworth, J; McCrae, WM; Scott, F1
Robinson, D1
Den Tandt, WR; Lassila, E; Philippart, M1
Hultbery, B; Ockerman, PA1
Nordén, NE; Ockerman, PA; Szabó, L1
Brun, A; Gamstorp, I; Kjellman, B; Ockerman, PA; Palmgren, B1
Dahlqvist, A; Hultberg, B; Ockerman, PA1
Atkins, L; Kanvfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE1

Reviews

5 review(s) available for mannose and Mucopolysaccharidoses

ArticleYear
[Metabolic disorders of glycoproteins in congenital glycosidase deficiencies].
    Seikagaku. The Journal of Japanese Biochemical Society, 1984, Volume: 56, Issue:5

    Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Fucose; G(M1) Ganglioside; Gangliosidoses; Glucosidases; Glycoproteins; Humans; Lactose Intolerance; Mannose; Mucolipidoses; Mucopolysaccharidoses; Neuraminidase; Oligosaccharides; Sandhoff Disease

1984
Mucopolysaccharidoses and mucolipidoses.
    Journal of clinical pathology. Supplement (Royal College of Pathologists), 1974, Volume: 8

    Topics: beta-Galactosidase; Cells, Cultured; Child, Preschool; Chondroitin Sulfates; Female; Fucose; Gangliosidoses; Genetic Carrier Screening; Hexosyltransferases; Humans; Iduronidase; Liver; Lysosomes; Mannose; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI

1974
The genetic mucolipidoses.
    Neuropadiatrie, 1970, Volume: 2, Issue:1

    Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child, Preschool; Fucose; Gangliosides; Glycosaminoglycans; Humans; Infant; Intellectual Disability; Mannose; Mucopolysaccharidoses; Sphingolipids; Sulfoglycosphingolipids

1970
Multiple forms of glycosidases in the normal and pathological states.
    Enzyme, 1974, Volume: 18, Issue:1

    Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses

1974
Prenatal genetic diagnosis. 3.
    The New England journal of medicine, 1970, Dec-31, Volume: 283, Issue:27

    Topics: Abortion, Induced; Acid Phosphatase; Adrenal Hyperplasia, Congenital; Amnion; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Congenital Abnormalities; Counseling; Culture Techniques; Cystic Fibrosis; Economics, Medical; Ethics, Medical; Female; Fetal Diseases; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Heterozygote; Homozygote; Humans; Lysosomes; Mannose; Marfan Syndrome; Methods; Mucopolysaccharidoses; Muscular Dystrophies; Porphyrias; Pregnancy; Punctures; Xeroderma Pigmentosum

1970

Other Studies

14 other study(ies) available for mannose and Mucopolysaccharidoses

ArticleYear
Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiency.
    The Journal of clinical investigation, 1975, Volume: 56, Issue:3

    Topics: Asparaginase; Aspartylglucosylaminase; Cells, Cultured; Child, Preschool; Disaccharidases; Extracellular Space; Fibroblasts; Glucosamine; Glycopeptides; Glycoproteins; Glycosaminoglycans; Glycosphingolipids; Humans; Male; Mannose; Mannosidases; Mucopolysaccharidoses; Skin

1975
Lectin histochemical study of lipopigments with special regard to neuronal ceroid-lipofuscinosis. Results with concanavalin A.
    Histochemistry, 1989, Volume: 93, Issue:2

    Topics: Adolescent; Adult; Animals; Ceroid; Child; Child, Preschool; Concanavalin A; Gangliosidoses; Humans; Lipofuscin; Mannose; Mucopolysaccharidoses; Neuronal Ceroid-Lipofuscinoses; Neurons; Olivary Nucleus; Pigments, Biological; Staining and Labeling

1989
Diseases of glycoprotein storage.
    Lancet (London, England), 1969, Apr-05, Volume: 1, Issue:7597

    Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Lipidoses; Liver; Mannose; Mucopolysaccharidoses

1969
White blood cell acid hydrolases in leukaemias, mucopolysaccharidoses and mannosidosis.
    Scandinavian journal of haematology, 1973, Volume: 10, Issue:4

    Topics: Adolescent; Adult; Aged; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gel; Female; Galactosidases; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoelectric Focusing; Leukemia, Lymphoid; Leukemia, Myeloid; Leukemia, Myeloid, Acute; Leukocytes; Male; Mannose; Methods; Middle Aged; Mucopolysaccharidoses

1973
Mannosidosis: detection of the disease and of heterozygotes using serum and leucocytes.
    Biochemical and biophysical research communications, 1974, Jan-23, Volume: 56, Issue:2

    Topics: Acetamides; Chromatography, DEAE-Cellulose; Contraceptives, Oral; Female; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Kinetics; Leukocytes; Male; Mannose; Mucopolysaccharidoses; Spectrometry, Fluorescence

1974
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
    Clinica chimica acta; international journal of clinical chemistry, 1969, Volume: 25, Issue:1

    Topics: Acid Phosphatase; Brain; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gel; Fucose; Galactosidases; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hot Temperature; Humans; Intellectual Disability; Kidney; Mannose; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Spleen

1969
The genetic mucolipidoses. Diagnosis and differential diagnosis.
    Humangenetik, 1970, Volume: 9, Issue:2

    Topics: Bone Marrow Examination; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Female; Fucose; Gangliosides; Glycolipids; Glycosaminoglycans; Hand; Hip; Humans; Infant; Leg; Lipid Metabolism; Male; Mannose; Mucopolysaccharidoses; Phospholipids; Radiography; Spine

1970
Lysosomal enzymes of cultured fibroblasts of cystic fibrosis patients.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 40, Issue:1

    Topics: Acetates; Acid Phosphatase; Arabinose; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Child; Chondroitin; Cystic Fibrosis; Fibroblasts; Fucose; Galactosidases; Glucosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Lysosomes; Mannose; Mucopolysaccharidoses

1972
Leroy's l-cell disease: markedly increased activity of plasma acid hydrolases.
    The Journal of laboratory and clinical medicine, 1974, Volume: 83, Issue:3

    Topics: Abnormalities, Multiple; Acid Phosphatase; Arabinose; Corneal Opacity; Cytoplasmic Granules; Fibroblasts; Galactosidases; Glucosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Intellectual Disability; Mannose; Metabolism, Inborn Errors; Mucopolysaccharidoses; Phosphoric Diester Hydrolases; Retinitis Pigmentosa; Skin

1974
Artificial substrates in the assay of acid glycosidases.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 39, Issue:1

    Topics: Chlorides; Chromatography, Gel; Enzyme Activation; Galactosidases; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoelectric Focusing; Lipidoses; Liver; Lysosomes; Macromolecular Substances; Mannose; Methods; Mucopolysaccharidoses; Osmolar Concentration; Retinitis Pigmentosa

1972
Urinary mannose in mannosidosis.
    The Journal of pediatrics, 1973, Volume: 82, Issue:4

    Topics: Acid Phosphatase; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography; Female; Galactosidases; Glucosidases; Glucuronidase; Glycoside Hydrolases; Hexosaminidases; Humans; Liver; Lysosomes; Mannose; Monosaccharides; Mucopolysaccharidoses

1973
Mannosidosis: isolation of oligosaccharide storage material from brain.
    The Journal of pediatrics, 1969, Volume: 75, Issue:3

    Topics: Amino Acids; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Chromatography; Chromatography, Gel; Diagnosis, Differential; Fucose; Galactose; Glucosamine; Glucose; Glycoside Hydrolases; Hexosamines; Humans; Liver; Mannose; Monosaccharides; Mucopolysaccharidoses; Neuraminic Acids; Oligosaccharides; Uronic Acids

1969
Mannosidosis: a clinical and histopathologic study.
    The Journal of pediatrics, 1969, Volume: 75, Issue:3

    Topics: Bone Marrow Cells; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Glucosamine; Glycoside Hydrolases; Humans; Infant; Liver; Lymph Nodes; Male; Mannose; Mucopolysaccharidoses; Radiography

1969
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