Page last updated: 2024-08-22

acetylglucosamine and Deficiency, Mental

acetylglucosamine has been researched along with Deficiency, Mental in 19 studies

Research

Studies (19)

Timeframe	Studies, this research(%)	All Research%
pre-1990	7 (36.84)	18.7374
1990's	8 (42.11)	18.2507
2000's	1 (5.26)	29.6817
2010's	1 (5.26)	24.3611
2020's	2 (10.53)	2.80

Authors

Authors	Studies
Blok, LER; Catinozzi, M; Czajewski, I; Fenckova, M; Ferenbach, AT; Mariappa, D; Muha, V; Schenck, A; Storkebaum, E; van Aalten, DMF	1
Olivier-Van Stichelen, S; Wenzel, DM	1
Roth, J; Taatjes, DJ	1
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
Iwakiri, N; Ohba, N; Sameshima, M; Uehara, F; Yanagita, T	1
Aronen, HJ; Autti, T; Haltia, M; Lauronen, L; Raininko, R; Salonen, O; Santavuori, P; Vanhanen, SL; Wirtavuori, K	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
Jaeken, J	1
Schmidt, H; Sewell, AC; Ullrich, K; von Lengerke, JH; Weglage, J; Ziegler, R	1

Reviews

1 review(s) available for acetylglucosamine and Deficiency, Mental

Article	Year
The O-GlcNAc cycling in neurodevelopment and associated diseases. Biochemical Society transactions, 2022, 12-16, Volume: 50, Issue:6 Topics: Acetylglucosamine; Animals; Glycosylation; Humans; Intellectual Disability; Mice; Mutation; N-Acetylglucosaminyltransferases; Protein Processing, Post-Translational; Signal Transduction	2022

Other Studies

18 other study(ies) available for acetylglucosamine and Deficiency, Mental

Article	Year
Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila. PLoS genetics, 2022, Volume: 18, Issue:5 Topics: Acetylglucosamine; Animals; Drosophila; Habituation, Psychophysiologic; Humans; Hydrolases; Intellectual Disability; N-Acetylglucosaminyltransferases; Protein Processing, Post-Translational	2022
In focus in HCB. Histochemistry and cell biology, 2018, Volume: 149, Issue:6 Topics: Acetylglucosamine; Adipocytes; Animals; Arrhythmias, Cardiac; Biomarkers, Tumor; Gastrointestinal Tract; Genetic Diseases, X-Linked; Gigantism; Heart Defects, Congenital; Humans; Intellectual Disability; Lectins; Phenotype; Polysaccharides; Stomach Neoplasms	2018
Five-year follow-up of two siblings with aspartylglucosaminuria undergoing allogeneic stem-cell transplantation from unrelated donors. Transplantation, 2004, Aug-15, Volume: 78, Issue:3 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. Journal of inherited metabolic disease, 1984, Volume: 7, Issue:3 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. American journal of medical genetics, 1984, Volume: 19, Issue:4 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. Helvetica paediatrica acta, 1981, Volume: 36, Issue:2 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. Journal of inherited metabolic disease, 1981, Volume: 4, Issue:4 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. Acta paediatrica (Oslo, Norway : 1992), 1995, Volume: 84, Issue:3 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. Acta paediatrica (Oslo, Norway : 1992), 1993, Volume: 82, Issue:5 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
Lectin-histochemical study of O-linked glycoconjugates in dysplastic retina of Norrie disease. Japanese journal of ophthalmology, 1996, Volume: 40, Issue:2 Topics: Acetylglucosamine; Antigens, Tumor-Associated, Carbohydrate; Eye Abnormalities; Female; Glycoconjugates; Histocytochemistry; Humans; Immunoenzyme Techniques; Infant; Intellectual Disability; Lectins; N-Acetylneuraminic Acid; Peanut Agglutinin; Polysaccharides; Retina; Retinal Dysplasia; Wheat Germ Agglutinins	1996
Aspartylglucosaminuria: radiologic course of the disease with histopathologic correlation. Journal of child neurology, 1997, Volume: 12, Issue:6 Topics: Acetylglucosamine; Adolescent; Adult; Age Factors; Aspartylglucosaminuria; Basal Ganglia; Brain; Case-Control Studies; Cerebral Cortex; Child; Child, Preschool; Female; Humans; Infant; Intellectual Disability; Lysosomal Storage Diseases; Magnetic Resonance Imaging; Male; Nerve Fibers, Myelinated; Neurons; Thalamus; Vacuoles	1997
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients. Human molecular genetics, 1998, Volume: 7, Issue:2 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. Experimental hematology, 1999, Volume: 27, Issue:9 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. Journal of inherited metabolic disease, 1978, Volume: 1, Issue:3 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. Clinical genetics, 1991, Volume: 40, Issue:4 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. Human genetics, 1991, Volume: 87, Issue:3 Topics: Acetylglucosamine; Aspartylglucosaminuria; Child; Finland; Humans; Intellectual Disability; Metabolism, Inborn Errors; Prevalence	1991
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins]. Verhandelingen - Koninklijke Academie voor Geneeskunde van Belgie, 1989, Volume: 51, Issue:4 Topics: Acetylglucosamine; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Demyelinating Diseases; Diseases in Twins; Female; Galactose; Glucosamine; Humans; Intellectual Disability; Sialic Acids; Syndrome; Twins, Monozygotic	1989
[Aspartylglucosaminuria. Clinical description of 2 German patients]. Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1989, Volume: 137, Issue:8 Topics: Abnormalities, Multiple; Acetylglucosamine; Adolescent; Amidohydrolases; Aspartylglucosaminuria; Child; Child Development; Female; Fibroblasts; Humans; Intellectual Disability; Leukocytes; Risk Factors	1989