fucose and Marfan Syndrome, Type I

fucose has been researched along with Marfan Syndrome, Type I in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (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
Federico, A; Guazzi, G	1

Reviews

1 review(s) available for fucose and Marfan Syndrome, Type I

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

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