01/01/1988 - "The data demonstrate that the analysis of glycoasparagines in amniotic fluid is not likely to permit reliable prenatal diagnosis of aspartylglycosaminuria."
01/01/1988 - "Midterm amniotic fluid samples from one pregnancy with the fetus affected by aspartylglycosaminuria and from 11 normal pregnancies were analysed for glycoasparagines accumulating in urine in aspartylglycosaminuria. "
01/01/1988 - "Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria."
03/10/1979 - "Accumulation of two glycoasparagines in the liver in aspartylglycosaminuria."
08/01/1976 - "Three different glycoasparagines have been isolated from the urine of a patient with aspartylglycosaminuria and their structures determined using sugar, amino acid and methylation analysis, enzymic degradation and measurements of the optical rotations. "
03/01/1997 - "These findings explain the accumulation of fucosylated and normal catabolism of nonfucosylated glycoasparagines in fucosidosis."
10/15/1991 - "Fucosyl glycoasparagines accumulating in the urine of a patient with fucosidosis were isolated using reverse-phase HPLC. "
10/15/1991 - "Characterization and 400-MHz 1H-NMR analysis of urinary fucosyl glycoasparagines in fucosidosis."
01/01/1978 - "Structure of the three major fucosyl-glycoasparagines accumulating in the urine of a patient with fucosidosis."
02/01/1978 - "The urinary excretion of fucose-containing material was found to be highly increased in a patient with fucosidosis type 2. Three structurally related compounds, a disaccharide and two glycoasparagines, were isolated from the urine. "
|3.||Lysosomal Storage Diseases (Lysosomal Storage Disease)
|4.||Gaucher Disease (Gaucher's Disease)