Compounds > fucose

fucose and Syndrome

fucose has been researched along with Syndrome in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19907 (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
Clausen, J; Dyggve, HV; Melchior, JC; Rastogi, SC1
Borrone, C; Durand, P; Gatti, R; Trias, X2
Beratis, NG; Danesino, C; Hirschhorn, K; Kousseff, BG1
Miller, CS; Reynolds, LW; Taylor, HA; Thomas, GH1
Atkins, L; Bartsocas, CS; Cosimi, B; Dulaney, JT; Fuller, TC; Janowska, S; Kliman, A; Moser, HW; O'Brien, JS; Russell, PS1
Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S1

Other Studies

7 other study(ies) available for fucose and Syndrome

ArticleYear
The Dyggve-Melchior-Clausen syndrome.
    Clinica chimica acta; international journal of clinical chemistry, 1977, Jul-01, Volume: 78, Issue:1

    Topics: Adult; Cells, Cultured; Dwarfism; Female; Fucose; Galactosamine; Glycoproteins; Glycosaminoglycans; Hexosamines; Humans; Hyaluronic Acid; Intellectual Disability; Leucine; Lymphocytes; Male; Mucopolysaccharidoses; Proteinuria; Syndrome; Time Factors; Uronic Acids

1977
Letter: Genetic heterogeneity in fucosidosis.
    Lancet (London, England), 1973, Nov-03, Volume: 302, Issue:7836

    Topics: Adolescent; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Ethnicity; Fabry Disease; Female; Fucose; Heterozygote; Humans; Infant; Leukocytes; Lewis Blood Group Antigens; Male; Mucopolysaccharidosis IV; Syndrome

1973
Letter: Genetic heterogeneity in fucosidosis.
    Lancet (London, England), 1973, Dec-15, Volume: 2, Issue:7842

    Topics: Bone Diseases, Developmental; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Fabry Disease; Face; Fucose; Humans; Intellectual Disability; Male; Syndrome

1973
Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.
    Pediatric research, 1973, Volume: 7, Issue:9

    Topics: Acetamides; Cells, Cultured; Electrophoresis, Starch Gel; Fibroblasts; Fucose; Galactosidases; Glycoside Hydrolases; Hexosaminidases; Humans; In Vitro Techniques; Lysosomes; Mannose; Methods; Mucopolysaccharidosis I; Skin; Spectrophotometry; Sulfatases; Syndrome; Temperature

1973
Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new cases.
    The Journal of pediatrics, 1974, Volume: 84, Issue:5

    Topics: Adolescent; Blood Group Antigens; Child; Consanguinity; Female; Fucose; Glycolipids; Glycoside Hydrolases; Humans; Immune Sera; Male; Mucopolysaccharidoses; Radiography; Saliva; Spine; Syndrome

1974
Infusion of normal HL-A identical leukocytes in Sanfilippo disease type B. Estimate of infused cell survival by assays of alpha-N-acetylglucosaminidase activity and cytogenetic techniques: effect on glycosaminoglycan excretion in the urine.
    Archives of neurology, 1974, Volume: 31, Issue:5

    Topics: Cell Survival; Chemical Phenomena; Chemistry; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 1-3; Cyclophosphamide; Fucose; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Histocompatibility Antigens; Histocompatibility Testing; HLA Antigens; Humans; Intellectual Disability; Leukocyte Transfusion; Leukocytes; Lymphocytes; Male; Mucopolysaccharidoses; Nitrophenols; Syndrome; Transplantation, Homologous

1974
Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
    European journal of clinical investigation, 1974, Dec-05, Volume: 4, Issue:6

    Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration

1974