1.
Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects
by Morelle, Willy
The journal of clinical endocrinology and metabolism, 2017, Vol.102 (4), p.1375-1386
2.
TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation
by Foulquier, François
American journal of human genetics, 2012, Vol.91 (1), p.15-26
3.
Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation
by Molinari, Florence
American journal of human genetics, 2008, Vol.82 (5), p.1150-1157
4.
Does O-GlcNAc play a role in neurodegenerative diseases?
by Lefebvre, Tony
Expert review of proteomics, 2005, Vol.2 (2), p.265-275
5.
FAB-MS characterization of sialyl Lewisx determinants on polylactosamine chains of human airway mucins secreted by patients suffering from cystic fibrosis or chronic bronchitis
by Willy Morelle
Glycoconjugate journal, 2001, Vol.18 (9), p.699
6.
FAB-MS characterization of sialyl Lewis super(x) determinants on polylactosamine chains of human airway mucins secreted by patients suffering from cystic fibrosis or chronic bronch...
by Morelle, Willy
Glycoconjugate journal, 2001, Vol.18 (9), p.699-708
7.
FAB-MS characterization of sialyl Lewis.sup.x determinants on polylactosamine chains of human airway mucins secreted by patients suffering from cystic fibrosis or chronic bronchiti...
by Morelle, Willy
Glycoconjugate journal, 2001, Vol.18 (9), p.699
