| SPEAKERS click on titles for presentation (Quicktime movies, Link to Quicktime) KEYNOTE ADDRESS The
Growing Impact of Glycobiology on Medicine GLYCOSYLATION-BASED MYOPATHIES The
PMT family of protein O-mannosyltransferases: from Synaptic
glycosylation and muscular dystrophy Studies
of the Metabolic Basis of Hereditary Inclusion Body Myopathy MOUSE MODELS OF HUMAN GLYCOSYLATION DISEASES A
Murine Model for Hereditary Multiple Exostosis (HME) Perlecan
gene mutations in two classes of skeletal dysplasias Pathophysiology
in fucosylation-defective mice Generation
of a mouse model for CDG-Ia CONGENITAL DISORDERS OF GLYCOSYLATION Congenital
Disorders of Glycosylation: Group III? New
types of CDG: Mannosyltransferase I deficiency and a CDG with
defective a2,3 sialylation Variability
of cellular responses and of clinical manifestations in ER-glycosylation
defects Some
tricks for the diagnosis of aberrant N-glycan glucosylation CDG PATIENTS AND PATIENCE Biochemical
Studies of Growth and Puberty in Congenital Disorders of Glycosylation Discovery
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