fucose has been researched along with Intellectual Disability in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 13 (86.67) | 18.7374 |
1990's | 1 (6.67) | 18.2507 |
2000's | 1 (6.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Frydman, M; Orlin, JB; Shalev, E; Vardimon, D | 1 |
Hirschberg, CB | 1 |
Clausen, J; Dyggve, HV; Melchior, JC; Rastogi, SC | 1 |
Beratis, NG; Danesino, C; Hirschhorn, K; Kousseff, BG | 1 |
Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
Borrone, C; Della Cella, G; Durand, P | 1 |
Spranger, JW; Wiedemann, HR | 1 |
Feleki, V; Gordon, BA | 1 |
O'Brien, JS | 1 |
Den Tandt, WR; Giesberts, MA | 1 |
Atkins, L; Bartsocas, CS; Cosimi, B; Dulaney, JT; Fuller, TC; Janowska, S; Kliman, A; Moser, HW; O'Brien, JS; Russell, PS | 1 |
Blümcke, S; Freitag, F; Küchemann, K | 1 |
Pollitt, RJ; Pretty, KM | 1 |
O'Brien, JS; Okada, S; Zielke, K | 1 |
Patel, V; Watanabe, I; Zeman, W | 1 |
2 review(s) available for fucose and Intellectual Disability
Article | Year |
---|---|
Golgi nucleotide sugar transport and leukocyte adhesion deficiency II.
Topics: Amino Acid Substitution; Animals; Arabs; Biological Transport; Carbohydrate Metabolism, Inborn Errors; Carrier Proteins; Cell Line; Child, Preschool; Consanguinity; Dimerization; DNA Mutational Analysis; Dogs; Ethnicity; Eukaryotic Cells; Fetal Growth Retardation; Fucose; Genetic Heterogeneity; Genetic Predisposition to Disease; Glycoproteins; Glycosylation; Golgi Apparatus; Guanosine Diphosphate Fucose; Humans; Infections; Intellectual Disability; Invertebrates; Lectins; Leukocyte-Adhesion Deficiency Syndrome; Male; Mammals; Monosaccharide Transport Proteins; Nucleoside Diphosphate Sugars; Phenotype; Point Mutation; Protein Processing, Post-Translational; Recurrence; Selection, Genetic; Turkey | 2001 |
The genetic mucolipidoses.
Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child, Preschool; Fucose; Gangliosides; Glycosaminoglycans; Humans; Infant; Intellectual Disability; Mannose; Mucopolysaccharidoses; Sphingolipids; Sulfoglycosphingolipids | 1970 |
13 other study(ies) available for fucose and Intellectual Disability
Article | Year |
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Prenatal diagnosis of Rambam-Hasharon syndrome.
Topics: Abortion, Induced; Blood Group Antigens; Chromosome Mapping; Consanguinity; Cordocentesis; Female; Fetal Diseases; Fucose; Genes, Recessive; Genetic Linkage; Humans; Immune System; Intellectual Disability; Leukocyte-Adhesion Deficiency Syndrome; Male; Metabolism, Inborn Errors; Phenotype; Pregnancy; Pregnancy Trimester, Second; Prenatal Diagnosis | 1996 |
The Dyggve-Melchior-Clausen syndrome.
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.
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 |
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
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 |
Fucosidosis.
Topics: Brain Diseases; Carbohydrate Metabolism, Inborn Errors; Cerebral Cortex; Female; Fucose; Glycosaminoglycans; Glycoside Hydrolases; Humans; Infant; Infant, Newborn; Intellectual Disability; Liver; Male; Microscopy, Electron; Muscular Diseases; Myocardium | 1969 |
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
Topics: Acid Phosphatase; Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Fucose; Galactosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Liver; Mannose; Mucopolysaccharidosis I; Sulfatases | 1970 |
Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
Topics: Acetates; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Female; Fibroblasts; Fucose; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Intellectual Disability; Kidney; Liver; Male; Mucopolysaccharidoses; Pregnancy; Retinitis Pigmentosa; Skin | 1972 |
Deficiency of lysosomal enzymes in storage diseases.
Topics: Acetates; Acid Phosphatase; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fucose; Galactosidases; Glucuronidase; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrolases; Infant; Intellectual Disability; Leukocytes; Lipid Metabolism, Inborn Errors; Liver; Lysosomes; Male; Middle Aged; Mucopolysaccharidoses; Sulfatases | 1973 |
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.
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 |
Hepatic ultrastructure in fucosidosis.
Topics: Biopsy; Brain Diseases; Capillaries; Cerebral Decortication; Child, Preschool; Epithelium; Fucose; Histiocytes; Humans; Inclusion Bodies; Intellectual Disability; Lipid Metabolism, Inborn Errors; Liver; Male; Microscopy, Electron | 1971 |
Glycoasparagines in the urine of patients with aspartylglycosaminuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Chromatography; Chromatography, Ion Exchange; Fucose; Galactose; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Molecular Weight | 1972 |
Fucosidosis: diagnosis by serum assay of alpha-L-fucosidase.
Topics: Buffers; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Clinical Enzyme Tests; Fucose; Glycoside Hydrolases; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Male; Methods; Temperature | 1972 |
Deficiency of alpha-L-fucosidase.
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Fucose; Glycoside Hydrolases; Humans; Intellectual Disability; Lysosomes; Male; Metabolism, Inborn Errors; Microscopy, Electron; Skin | 1972 |