Compounds > acetylglucosamine

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acetylglucosamine and Amino Acid Metabolism Disorders, Inborn

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

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	4 (57.14)	18.2507
2000's	1 (14.29)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Malm, G; Månsson, JE; Mosskin, M; Ringdén, O; Winiarski, J	1
Maury, CP	1
Dunder, U; Groffen, J; Heisterkamp, N; Kuronen, I; Mononen, I; Noronkoski, T; Romppanen, EL	1
Aula, P; Gray, GR; Keulemans, JL; Kleijer, WJ; van Diggelen, OP	1
Fahlman, C; Jalanko, A; Karlsson, S; Laine, M; Peltonen, L; Rapola, J; Renlund, M; Richter, J	1
Dilling, LA; Haworth, JC; Seargeant, LE	1
Rudy, JL	1

Other Studies

7 other study(ies) available for acetylglucosamine and Amino Acid Metabolism Disorders, Inborn

Article	Year
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
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
Recombinant glycosylasparaginase and in vitro correction of aspartylglycosaminuria. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 1995, Volume: 9, Issue:5 Topics: 3T3 Cells; Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Animals; Aspartylglucosylaminase; Biological Transport; Cell Line, Transformed; Humans; Lymphocytes; Mice; Recombinant Proteins	1995
Applications of a new fluorimetric enzyme assay for the diagnosis of aspartylglucosaminuria. Journal of inherited metabolic disease, 1993, Volume: 16, Issue:6 Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Aspartylglucosylaminase; Chorionic Villi; Female; Fibroblasts; Fluorometry; Genetic Carrier Screening; Humans; Leukocytes; Pregnancy; Prenatal Diagnosis; Substrate Specificity	1993
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 presenting with hepatosplenomegaly in early infancy. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:6 Topics: Acetylglucosamine; Amino Acid Metabolism, Inborn Errors; Female; Hepatomegaly; Humans; Infant, Newborn; Splenomegaly	1992
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