Wendy Vleugels

DPM2‐CDG: A muscular dystrophy–dystroglycanopathy syndrome with severe epilepsy

Rita Barone, Chiara Aiello, Valérie Race et al. · Annals of Neurology · 2012 · 149 citations

Mammalian Phosphomannomutase PMM1 Is the Brain IMP-sensitive Glucose-1,6-bisphosphatase

Maria Veiga‐da‐Cunha, Wendy Vleugels, Pushpa Maliekal et al. · Journal of Biological Chemistry · 2008 · 44 citations · Full text

RFT1 deficiency in three novel CDG patients

Wendy Vleugels, Micha A. Haeuptle, Bobby G. Ng et al. · Human Mutation · 2009 · 37 citations

The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

K. Cromphout, Wendy Vleugels, Leen Heykants et al. · Molecular and Cellular Biology · 2006 · 36 citations · Full text

Genetics, Glycobiology, Normal Phenotype +17

RFT1‐CDG: Deafness as a novel feature of congenital disorders of glycosylation

J. Jaeken, Wendy Vleugels, Luc Régal et al. · Journal of Inherited Metabolic Disease · 2009 · 32 citations · Full text