1 – 10 of 13
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2017
-
Mark
Screening protocols to monitor respiratory status in primary immunodeficiency disease : findings from a European survey and subclinical infection working group
(
- Contribution to journal › Article
- 2015
-
Mark
The role of the prostate cancer gene 3 urine test in addition to serum prostate-specific antigen level in prostate cancer screening among breast cancer, early-onset gene mutation carriers
(
- Contribution to journal › Article
- 2011
-
Mark
Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer : Preliminary analysis of the results of the IMPACT study
(
- Contribution to journal › Article
- 2010
-
Mark
Charged-particle multiplicities in pp interactions at root s=900 GeV measured with the ATLAS detector at the LHC ATLAS Collaboration
2010) In Physics Letters. Section B: Nuclear, Elementary Particle and High-Energy Physics 688(1). p.21-42(
- Contribution to journal › Article
- 2007
-
Mark
Breath alcohol concentration determined with a new analyzer using free exhalation predicts almost precisely the arterial blood alcohol concentration.
(
- Contribution to journal › Article
- 2001
-
Mark
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency
(
- Contribution to journal › Article
-
Mark
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
(
- Contribution to journal › Article
- 2000
-
Mark
V(D)J recombination defects in lymphocytes: a severe immunodeficiency with a spectrum of clinical presentations due to Rag mutations
(
- Contribution to journal › Published meeting abstract
- 1998
-
Mark
Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome.
(
- Contribution to journal › Published meeting abstract
-
Mark
Report of the ESID collaborative study on clinical features and molecular analysis in X-linked hyper-IgM syndrome
(
- Contribution to journal › Published meeting abstract