glucosamine has been researched along with AGA Deficiency in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 17 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ammälä, P; Aula, P; Rapola, J; von Koskull, H | 1 |
| Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 2 |
| Maury, CP | 2 |
| Maury, P; Palo, J | 1 |
| Marnela, KM | 1 |
| Maury, CP; Palo, J | 1 |
| Borud, O; Lie, SO; Strömme, JH; Torp, KH | 1 |
| Borud, O; Torp, KH | 1 |
| Borud, O; Dahl, T; Torp, KH | 1 |
| Akasaki, M; Aula, P; Funakoshi, I; Sugahara, K; Yamashina, I | 1 |
| Aula, P; Funakoshi, I; Funakoshi, S; Sugahara, K; Yamashina, I | 1 |
| Mononen, TK | 1 |
| Heino, J; Larjava, H; Näntö-Salonen, K; Pelliniemi, LJ; Penttinen, R; Säämanen, AM; Tammi, M | 1 |
| Alfthan, G; Halme, T; Langevelde, FV; Näntö-Salonen, K; Penttinen, R; Vis, RD | 1 |
| Mononen, I; Mononen, T; Parviainen, M; Penttilä, I | 1 |
17 other study(ies) available for glucosamine and AGA Deficiency
| Article | Year |
|---|---|
Prenatal diagnosis and fetal pathology of aspartylglucosaminuria.
Topics: Acetylglucosamine; Amidohydrolases; Amniotic Fluid; Aspartylglucosaminuria; Aspartylglucosylaminase; Cells, Cultured; Chorionic Villi; Female; Fetus; Glucosamine; Heterozygote; Humans; Lysosomes; Male; Pregnancy; Prenatal Diagnosis | 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 |
Detection of aspartylglycosaminuria by gas--liquid chromatography.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Glucosamine; Humans; Middle Aged | 1981 |
Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Female; Gas Chromatography-Mass Spectrometry; Glucosamine; Humans; Lymphocytes; Vacuoles | 1980 |
Automated ion-exchange chromatography in the detection of aspartylglucosaminuria.
Topics: Acetylglucosamine; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Autoanalysis; Chromatography, Ion Exchange; Glucosamine; Humans; Microchemistry | 1980 |
Accumulation of glycoprotein-derived metabolites in neural and visceral tissue in aspartylglycosaminuria.
Topics: Acetylglucosamine; Amidohydrolases; Asparagine; Aspartylglucosaminuria; Glucosamine; Humans; Kidney; Nerve Tissue; Oligosaccharides; Spleen; Thyroid Gland; Tissue Distribution | 1980 |
N-Acetylglucosamine-asparagine levels in tissues of patients with aspartylglycosaminuria.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Asparagine; Aspartic Acid; Aspartylglucosaminuria; Endocytosis; Female; Glucosamine; Glycoproteins; Humans; Lysosomes; Male; Tissue Distribution | 1980 |
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 |
[Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Finland; Glucosamine; Humans; Infant; Intellectual Disability; Male; Norway | 1978 |
Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation.
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Glucosamine; Humans; Intellectual Disability; Mucolipidoses | 1978 |
Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU).
Topics: Acetylglucosamine; Amidohydrolases; Asparagine; Aspartylglucosaminuria; Gas Chromatography-Mass Spectrometry; Glucosamine; Hexosaminidases; Humans; Mannose; Mannosidases; Oligosaccharides | 1976 |
Characterization of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU).
Topics: Amidohydrolases; Asparagine; Aspartylglucosaminuria; Galactose; Galactosidases; Glucosamine; Metabolism, Inborn Errors; Neuraminidase; Sialic Acids | 1975 |
Aspartylglucosamine excretion in heterozygous carriers of aspartylglycosaminuria.
Topics: Acetylglucosamine; Amidohydrolases; Aspartylglucosaminuria; Glucosamine; Heterozygote; Humans | 1989 |
Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Chondroitin Lyases; Chondroitin Sulfates; Collagen; Dermatan Sulfate; Electrophoresis, Polyacrylamide Gel; Female; Glucosamine; Glucuronates; Glucuronic Acid; Heparitin Sulfate; Humans; Male; Microscopy, Electron; Proteoglycans; Skin | 1987 |
Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Cells, Cultured; Child; Copper; Female; Fibroblasts; Glucosamine; Hair; Humans; Male; Metabolism, Inborn Errors; Zinc | 1985 |
Liquid-chromatographic detection of aspartylglycosaminuria.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female; Glucosamine; Humans; Infant; Male | 1986 |