n-acetylglucosaminylasparagine has been researched along with Intellectual Disability in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (46.15) | 18.7374 |
| 1990's | 6 (46.15) | 18.2507 |
| 2000's | 1 (7.69) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Malm, G; Månsson, JE; Mosskin, M; Ringdén, O; Winiarski, J | 1 |
| Autio, S; Härö, E; Kivimäki, T; Koskela, SL; Näntö, V; Näntö-Salonen, K; Penttinen, R | 1 |
| Caprari, P; Di Dio, R; Musumeci, S; Salvati, A; Salvo, G; Schiliró, G | 1 |
| Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 2 |
| Airaksinen, E; Kääriäinen, R; Launiala, K; Matilainen, R; Mononen, T | 1 |
| Arvio, M | 1 |
| Autti, T; Ginns, EI; Ikonen, S; Jalanko, A; Joensuu, R; LaMarca, ME; Manninen, T; McKinney, CE; Peltonen, L; Rapola, J; Riekkinen, P; Sipilä, I; Tenhunen, K | 1 |
| Fahlman, C; Jalanko, A; Karlsson, S; Laine, M; Peltonen, L; Rapola, J; Renlund, M; Richter, J | 1 |
| Borud, O; Lie, SO; Strömme, JH; Torp, KH | 1 |
| Hirabayashi, Y; Ikeda, S; Tsuji, S; Yamauchi, T; Yanagisawa, N; Yoshida, K | 1 |
| Airaksinen, E; Matilainen, R; Mononen, I; Mononen, T | 1 |
| Schmidt, H; Sewell, AC; Ullrich, K; von Lengerke, JH; Weglage, J; Ziegler, R | 1 |
13 other study(ies) available for n-acetylglucosaminylasparagine and Intellectual Disability
| Article | Year |
|---|---|
Five-year follow-up of two siblings with aspartylglucosaminuria undergoing allogeneic stem-cell transplantation from unrelated donors.
Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Intellectual Disability; Male; Siblings; Stem Cell Transplantation; Time Factors; Tissue Donors; Transplantation, Homologous | 2004 |
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline.
Topics: Acetylglucosamine; Adolescent; Adult; Age Factors; Child; Child, Preschool; Collagen; Connective Tissue Diseases; Female; Glucosamine; Humans; Hydroxyproline; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Middle Aged; Reference Values | 1984 |
Homozygous NADH-methemoglobin reductase and aspartylglucosaminidase deficiencies in a moderately retarded Sicilian child.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Cytochrome-B(5) Reductase; Female; Humans; Intellectual Disability; Male; Methemoglobinemia; NADH, NADPH Oxidoreductases; Pedigree | 1984 |
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull | 1981 |
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Consanguinity; Female; Glucosamine; Humans; Intellectual Disability; Leukocytes; Male; Oligosaccharides; Pedigree | 1981 |
A population-based study on the causes of mild and severe mental retardation.
Topics: Acetylglucosamine; Age Factors; Asphyxia Neonatorum; Case-Control Studies; Cerebral Hemorrhage; Child; Down Syndrome; Female; Fetal Alcohol Spectrum Disorders; Fetal Diseases; Finland; Fragile X Syndrome; Humans; Hypoglycemia; Infant, Newborn; Infections; Intellectual Disability; Male | 1995 |
Follow-up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions.
Topics: Acetylglucosamine; Adolescent; Adult; Aspartylglucosaminuria; Case-Control Studies; Child; Child Development; Child, Preschool; Female; Follow-Up Studies; Humans; Infant; Intellectual Disability; Intelligence Tests; Lysosomal Storage Diseases; Male; Middle Aged | 1993 |
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
Topics: Acetylglucosamine; Animals; Aspartylglucosaminuria; Aspartylglucosylaminase; Brain; Disease Models, Animal; Disease Progression; Gene Targeting; Genes, Recessive; Humans; Intellectual Disability; Liver; Lysosomal Storage Diseases; Magnetic Resonance Imaging; Maze Learning; Mice; Mice, Knockout; Microscopy, Electron; Phenotype | 1998 |
Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation.
Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Animals; Aspartylglucosaminuria; Aspartylglucosylaminase; Bone Marrow Transplantation; Brain; Humans; Intellectual Disability; Kidney; Liver; Lysosomal Storage Diseases; Lysosomes; Mice; Mice, Inbred C57BL; Mice, Knockout; Nerve Tissue Proteins; Organ Specificity; Polymerase Chain Reaction; Radiation Chimera; Specific Pathogen-Free Organisms; Spleen; Vacuoles | 1999 |
Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Creatinine; Dietary Proteins; Female; Glucosamine; Humans; Intellectual Disability; Male; Mucolipidoses | 1978 |
Two Japanese cases with aspartylglycosaminuria: clinical and morphological features.
Topics: Acetylglucosamine; Adult; Angiokeratoma; Aspartylglucosaminuria; Carbohydrate Sequence; Epilepsies, Myoclonic; Female; Humans; Intellectual Disability; Japan; Molecular Sequence Data; Oligosaccharides; Rectum; Skin Neoplasms | 1991 |
High prevalence of aspartylglycosaminuria among school-age children in eastern Finland.
Topics: Acetylglucosamine; Aspartylglucosaminuria; Child; Finland; Humans; Intellectual Disability; Metabolism, Inborn Errors; Prevalence | 1991 |
[Aspartylglucosaminuria. Clinical description of 2 German patients].
Topics: Abnormalities, Multiple; Acetylglucosamine; Adolescent; Amidohydrolases; Aspartylglucosaminuria; Child; Child Development; Female; Fibroblasts; Humans; Intellectual Disability; Leukocytes; Risk Factors | 1989 |