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Martin Hasilik

University of Göttingen

5

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A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis

2003 Journal of Biological Chemistry
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Deficiency of UDP-galactose:N-acetylglucosamine β-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId

2002 Journal of Clinical Investigation
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PHOSPHOMANNOSE-ISOMERASE (PMI) DEFICIENCY, A NEW DEFECT IN THE SYNTHESIS OF GLYCOPROTEINS, MAINLY MANIFESTS AS GASTROINTESTINAL DISEASE, WHICH CAN BE SUCCESSFULLY TREATED BY ORAL MANNOSE.

1998 Journal of Pediatric Gastroenterology and Nutrition
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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.

1998 Journal of Clinical Investigation
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Citations (350)