Page last updated: 2024-08-22

mannose and Enteropathy, Exudative

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

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
de Lonlay, P; Seta, N1
Damen, G; de Klerk, H; den Hollander, J; Huijmans, J; Sinaasappel, M1
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, KP1
Houwen, RH; Oren, A1

Other Studies

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

ArticleYear
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