fucose and Glycogenosis

fucose has been researched along with Glycogenosis 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
Sewell, AC	1
Federico, A; Guazzi, G	1
Robinson, D	1
Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S	1

Reviews

2 review(s) available for fucose and Glycogenosis

Article	Year
Urinary oligosaccharides in lysosomal and other metabolic disorders. Italian journal of neurological sciences, 1982, Volume: 3, Issue:1 Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glycogen Storage Disease; Humans; Mannose; Marfan Syndrome; Mass Screening; Metabolism, Inborn Errors; Mucolipidoses; Oligosaccharides; Osteogenesis Imperfecta; Sandhoff Disease; Tay-Sachs Disease	1982
Multiple forms of glycosidases in the normal and pathological states. Enzyme, 1974, Volume: 18, Issue:1 Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses	1974

Article

Year

Urinary oligosaccharides in lysosomal and other metabolic disorders.

Italian journal of neurological sciences, 1982, Volume: 3, Issue:1

Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glycogen Storage Disease; Humans; Mannose; Marfan Syndrome; Mass Screening; Metabolism, Inborn Errors; Mucolipidoses; Oligosaccharides; Osteogenesis Imperfecta; Sandhoff Disease; Tay-Sachs Disease

1982

Multiple forms of glycosidases in the normal and pathological states.

Enzyme, 1974, Volume: 18, Issue:1

Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses

1974

Other Studies

2 other study(ies) available for fucose and Glycogenosis

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
Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease). European journal of clinical investigation, 1974, Dec-05, Volume: 4, Issue:6 Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration	1974

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

Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).

European journal of clinical investigation, 1974, Dec-05, Volume: 4, Issue:6

Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration

1974