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(1 - 3 of 3)
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
Barzaghi, F.; Hernandez, L.C.A.; Neven, B.; Ricci, S.; Kucuk, Z.Y.; Bleesing, J.J.; ... ; European Soc Blood Marrow 2018
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study
Article / Letter to editor
open access
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
Dhekne, H.S.; Pylypenko, O.; Overeem, A.W.; Ferreira, R.J.; Velde, K.J. van der; Rings, E.H.H.M.; ... ; IJzendoorn, S.C.D. van 2018
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
Article / Letter to editor
open access
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
Gathmann, B.; Mahlaoui, N.; Gerard, L.; Oksenhendler, E.; Warnatz, K.; Schulze, I.; ... ; European Soc Immunodeficiencies 2014
Clinical picture and treatment of 2212 patients with common variable immunodeficiency
Article / Letter to editor
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