Compounds > mannose

Page last updated: 2024-08-22

mannose and Enteropathy, Exudative

mannose has been researched along with Enteropathy, Exudative in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (50.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Lonlay, P; Seta, N	1
Damen, G; de Klerk, H; den Hollander, J; Huijmans, J; Sinaasappel, M	1
Alton, G; Freeze, HH; Harms, E; Harms, HK; Hasilik, M; Koch, HG; Körner, C; Marquardt, T; Niehues, R; Reiter, K; Schiebe-Sukumar, M; von Figura, K; Wu, R; Zimmer, KP	1
Houwen, RH; Oren, A	1

Other Studies

4 other study(ies) available for mannose and Enteropathy, Exudative

Article	Year
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib. Biochimica et biophysica acta, 2009, Volume: 1792, Issue:9 Topics: Child, Preschool; Congenital Disorders of Glycosylation; Female; Glycosylation; Heparin; Humans; Infant; Mannose; Mannose-6-Phosphate Isomerase; Protein-Losing Enteropathies; Young Adult	2009
Gastrointestinal and other clinical manifestations in 17 children with congenital disorders of glycosylation type Ia, Ib, and Ic. Journal of pediatric gastroenterology and nutrition, 2004, Volume: 38, Issue:3 Topics: Adolescent; Adult; Age of Onset; Alanine Transaminase; Blood Coagulation Disorders; Child; Child, Preschool; Congenital Disorders of Glycosylation; Duodenum; Failure to Thrive; Female; Glucosyltransferases; Glycosylation; Hepatomegaly; Humans; Infant; Liver; Liver Cirrhosis; Male; Mannose; Mannose-6-Phosphate Isomerase; Netherlands; Phosphotransferases (Phosphomutases); Protein-Losing Enteropathies; Retrospective Studies	2004
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy. The Journal of clinical investigation, 1998, Apr-01, Volume: 101, Issue:7 Topics: Cells, Cultured; Glycoproteins; Glycosylation; Humans; Infant; Male; Mannose; Mannose-6-Phosphate Isomerase; Mutation; Protein Processing, Post-Translational; Protein-Losing Enteropathies; Syndrome; Transferrin	1998
Phosphomannoseisomerase deficiency as the cause of protein-losing enteropathy and congenital liver fibrosis. Journal of pediatric gastroenterology and nutrition, 1999, Volume: 29, Issue:2 Topics: Congenital Disorders of Glycosylation; Humans; Infant; Liver Cirrhosis; Mannose; Mannose-6-Phosphate Isomerase; Protein-Losing Enteropathies	1999