Esther van de Vosse
Department of Infectious Diseases
C5-P, Leiden University Medical Center
Albinusdreef 2
Netherlands
Name/email consistency: high
- Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation. van de Vosse, E., Verhard, E.M., Tool, A.J., de Visser, A.W., Kuijpers, T.W., Hiemstra, P.S., van Dissel, J.T. Ann. Hematol. (2011)
- Mycobacterium bovis BCG-itis and cervical lymphadenitis due to Salmonella enteritidis in a patient with complete interleukin-12/-23 receptor beta1 deficiency. van de Vosse, E., Ottenhoff, T.H., de Paus, R.A., Verhard, E.M., de Boer, T., van Dissel, J.T., Kuijpers, T.W. Infection (2010)
- Distribution of CFTR variations in an Indonesian enteric fever cohort. van de Vosse, E., de Visser, A.W., Al-Attar, S., Vossen, R., Ali, S., van Dissel, J.T. Clin. Infect. Dis. (2010)
- A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation. van de Vosse, E., van Wengen, A., van Geelen, J.A., de Boer, M., Roos, D., van Dissel, J.T. J. Hum. Genet. (2009)
- Antisense-mediated exon skipping to correct IL-12Rbeta1 deficiency in T cells. van de Vosse, E., Verhard, E.M., de Paus, R.A., Platenburg, G.J., van Deutekom, J.C., Aartsma-Rus, A., van Dissel, J.T. Blood (2009)
- Genetic deficiencies of innate immune signalling in human infectious disease. van de Vosse, E., van Dissel, J.T., Ottenhoff, T.H. Lancet. Infect. Dis (2009)
- Targets of anticytokine therapy and the risk of infections in humans and mice. van de Vosse, E., van Agtmael, M.A. Curr. Opin. Rheumatol (2007)
- Susceptibility to typhoid fever is associated with a polymorphism in the cystic fibrosis transmembrane conductance regulator (CFTR). van de Vosse, E., Ali, S., de Visser, A.W., Surjadi, C., Widjaja, S., Vollaard, A.M., van Dissel, J.T. Hum. Genet. (2005)
- Molecular complementation of IL-12Rbeta1 deficiency reveals functional differences between IL-12Rbeta1 alleles including partial IL-12Rbeta1 deficiency. van de Vosse, E., de Paus, R.A., van Dissel, J.T., Ottenhoff, T.H. Hum. Mol. Genet. (2005)
