Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation

Por van de Vosse, Esther, Verhard, Els M., Tool, Anton J. T., de Visser, Adriëtte W., Kuijpers, Taco W., Hiemstra, Pieter S., van Dissel, Jaap T.
Publicado em 2010

Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients

Por Alinejad Dizaj, Maryam, Mortaz, Esmaeil, Mahdaviani, Seyed Alireza, Mansouri, Davood, Mehrian, Payam, Verhard, Els M., Varahram, Mohammad, Babaie, Delara, Adcock, Ian M., Garssen, Johan, van de Vosse, Esther, Velayati, Aliakbar
Publicado no Immunogenetics (2017)

Deletion of the entire interferon-γ receptor 1 gene causing complete deficiency in three related patients

Por de Vor, Inge C., van der Meulen, Pomme M., Bekker, Vincent, Verhard, Els M., Breuning, Martijn H., Harnisch, Esther, van Tol, Maarten J. D., Wieringa, Jantien W., van de Vosse, Esther, Bredius, Robbert G. M.
Publicado no J Clin Immunol (2016)