fucose and Ganglioside Storage Diseases

fucose has been researched along with Ganglioside Storage Diseases in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (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
Yamashita, K	1
Sewell, AC	1
Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI	1
Van Hoof, F	1

Reviews

3 review(s) available for fucose and Ganglioside Storage Diseases

Article	Year
[Metabolic disorders of glycoproteins in congenital glycosidase deficiencies]. Seikagaku. The Journal of Japanese Biochemical Society, 1984, Volume: 56, Issue:5 Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Fucose; G(M1) Ganglioside; Gangliosidoses; Glucosidases; Glycoproteins; Humans; Lactose Intolerance; Mannose; Mucolipidoses; Mucopolysaccharidoses; Neuraminidase; Oligosaccharides; Sandhoff Disease	1984
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases. Advances in experimental medicine and biology, 1976, Volume: 68 Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses	1976
Mucopolysaccharidoses and mucolipidoses. Journal of clinical pathology. Supplement (Royal College of Pathologists), 1974, Volume: 8 Topics: beta-Galactosidase; Cells, Cultured; Child, Preschool; Chondroitin Sulfates; Female; Fucose; Gangliosidoses; Genetic Carrier Screening; Hexosyltransferases; Humans; Iduronidase; Liver; Lysosomes; Mannose; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI	1974

Other Studies

1 other study(ies) available for fucose and Ganglioside Storage Diseases

Article	Year
Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis. European journal of pediatrics, 1980, Volume: 134, Issue:3 Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Thin Layer; Fucose; Gangliosidoses; Germany, West; Glycogen; Glycogen Storage Disease; Glycolipids; Glycoproteins; Humans; Infant; Mannosidases; Mass Screening; Mucolipidoses; Oligosaccharides	1980

Article

Year

Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.

European journal of pediatrics, 1980, Volume: 134, Issue:3

Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Thin Layer; Fucose; Gangliosidoses; Germany, West; Glycogen; Glycogen Storage Disease; Glycolipids; Glycoproteins; Humans; Infant; Mannosidases; Mass Screening; Mucolipidoses; Oligosaccharides

1980