Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature

por Robyns, T, Nuyens, D, Van Casteren, L, Corveleyn, A, De Ravel, T, Heidbuchel, H, Willems, R
Publicado 2014

Terminal Complement Pathway Deficiency in an Adult Patient with Meningococcal Sepsis

por Staels, F., Meersseman, W., Stordeur, P., Willekens, K., Van Loo, S., Corveleyn, A., Meyts, I., Meyfroidt, G., Schrijvers, R.
Publicado 2022

Shwachman-Diamond Syndrome: frequent misdiagnosis as Jeune Syndrome and other peculiarities

por Meyts, I, Schaballie, H, Haerynck, F, Sevenants, L, Vermylen, C, Bordon, V, Bossuyt, X, Corveleyn, A, Uyttebroeck, A, Renard, M
Publicado 2011