Page last updated: 2024-08-22

glucosamine and Amino Acid Metabolism Disorders, Inborn

glucosamine has been researched along with Amino Acid Metabolism Disorders, Inborn in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	7 (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

Authors	Studies
Maury, CP	1
Borud, O; Torp, KH	1
Rudy, JL	1
Autio, S	1
Arstila, AU; Autio, S; Palo, J; Riekkinen, P	1
Humbel, R; Marchal, C	1
Autio, S; Iivanainen, M; Palo, J; Visakorpi, JK	1

Reviews

1 review(s) available for glucosamine and Amino Acid Metabolism Disorders, Inborn

Article	Year
Aspartylglycosaminuria. Analysis of thirty-four patients. Journal of mental deficiency research, 1972, Volume: 1, Issue:0 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Birth Order; Birth Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Electrocardiography; Electroencephalography; Female; Finland; Geography; Glucosamine; Humans; Infant; Intellectual Disability; Intelligence Tests; Life Expectancy; Male; Pedigree; Socioeconomic Factors	1972

Article

Year

Aspartylglycosaminuria. Analysis of thirty-four patients.

Journal of mental deficiency research, 1972, Volume: 1, Issue:0

Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Birth Order; Birth Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Electrocardiography; Electroencephalography; Female; Finland; Geography; Glucosamine; Humans; Infant; Intellectual Disability; Intelligence Tests; Life Expectancy; Male; Pedigree; Socioeconomic Factors

1972

Other Studies

6 other study(ies) available for glucosamine and Amino Acid Metabolism Disorders, Inborn

Article	Year
Detection of aspartylglycosaminuria by gas--liquid chromatography. Clinical chemistry, 1981, Volume: 27, Issue:12 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
[Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1978, Aug-30, Volume: 98, Issue:24 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 diagnosed by routine urine amino acid assay. Clinical chemistry, 1988, Volume: 34, Issue:10 Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Diagnostic Tests, Routine; Glucosamine; Glycoside Hydrolases; Humans	1988
Biochemical and fine structural studies in aspartylglucosaminuria. Monographs in human genetics, 1972, Volume: 6 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Aspartate Aminotransferases; Bone Diseases; Brain; Glucosamine; Hexosaminidases; Humans; Infections; Intellectual Disability; Liver	1972
Screening test for aspartylglycosaminuria. The Journal of pediatrics, 1974, Volume: 84, Issue:3 Topics: Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Aminoglycosides; Aspartic Acid; Chromatography, Thin Layer; Glucosamine; Humans; Methods	1974
Aspartylglucosaminuria, clinical aspects. Acta paediatrica Scandinavica. Supplement, 1970, Volume: 206 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Child, Preschool; Female; Glucosamine; Humans; Male	1970