Reply to Leao-Teles et al

Por Morava, Eva, Guillard, Maïlys, Lefeber, Dirk J, Wevers, Ron A
Publicado em 2010

Autosomal recessive cutis laxa syndrome revisited

Por Morava, Éva, Guillard, Maïlys, Lefeber, Dirk J, Wevers, Ron A
Publicado em 2009

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I

Por Guillard, Mailys, Wada, Yoshinao, Hansikova, Hana, Yuasa, Isao, Vesela, Katerina, Ondruskova, Nina, Kadoya, Machiko, Janssen, Alice, Van den Heuvel, Lambertus P. W. J., Morava, Eva, Zeman, Jiri, Wevers, Ron A., Lefeber, Dirk J.
Publicado em 2011

Deficiency of Dol-P-Man Synthase Subunit DPM3 Bridges the Congenital Disorders of Glycosylation with the Dystroglycanopathies

Por Lefeber, Dirk J., Schönberger, Johannes, Morava, Eva, Guillard, Mailys, Huyben, Karin M., Verrijp, Kiek, Grafakou, Olga, Evangeliou, Athanasios, Preijers, Frank W., Manta, Panagiota, Yildiz, Jef, Grünewald, Stephanie, Spilioti, Martha, van den Elzen, Christa, Klein, Dominique, Hess, Daniel, Ashida, Hisashi, Hofsteenge, Jan, Maeda, Yusuke, van den Heuvel, Lambert, Lammens, Martin, Lehle, Ludwig, Wevers, Ron A.
Publicado em 2009