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    Article

    Inflammation and the bone-vascular axis in end-stage renal disease

    Bone loss and vascular calcification coincide in patients with end-stage renal disease, similar as to what is observed in the general population. In the present bone biopsy study, we provide further evidence t...

    L. Viaene, G. J. Behets, S. Heye, K. Claes, D. Monbaliu in Osteoporosis International (2016)

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    Article

    Retrospective observational study on the incidence of incisional hernias after colorectal carcinoma resection with follow-up CT scan

    Incisional hernia (IH) is the most frequent complication after colorectal carcinoma (CRC) resection. The incidence depends on the method of follow-up, where ultrasound yields a significant number of additional...

    K. Claes, R. Beckers, E. Heindryckx, I. Kyle-Leinhase, P. Pletinckx, D. Claeys in Hernia (2014)

  3. Article

    Open Access

    Impact of early parenteral nutrition on catabolism

    J Gunst, I Vanhorebeek, MP Casaer, G Hermans, PJ Wouters, J Dubois in Critical Care (2013)

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    Chapter

    Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT

    Fabry disease is an X-linked inborn error of glycosphingolipid metabolism caused by quantitative or qualitative defects in the lysosomal enzyme alfa-Galactosidase A (aGAL A), ultimately resulting in vital orga...

    W. Terryn M.D., R. Vanholder, D. Hemelsoet in JIMD Reports - Case and Research Reports, … (2013)

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    Article

    Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testing

    Despite extensive analysis of the BRCA1 and BRCA2 genes, germline mutations are detected in <20% of families with a presumed genetic predisposition for breast and ovarian cancer. Recent literature reported RAD51C

    K. De Leeneer, M. Van Bockstal, S. De Brouwer in Breast Cancer Research and Treatment (2012)

  6. Article

    Open Access

    Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families

    Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma, yet mutations do not appear to be associated with an increased risk for breast cancer. We studied ovarian and breast cance...

    D J Osher, K De Leeneer, G Michils, N Hamel, E Tomiak, B Poppe in British Journal of Cancer (2012)

  7. Article

    Open Access

    P14.07 Qtc Interval Duration is Associated with Vascular Calcification in Renal Transplant Candidates

    Approximately 60% of all cardiac deaths in patients on dialysis are due to sudden death. Prolonged QT interval and arterial calcification have been associated with morbidity and mortality in different patient ...

    K. Claes, D. Mesotten, S. Heye, B. Bammens, P. Evenepoel in Artery Research (2010)

  8. Article

    Open Access

    A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

    L Bossini-Castillo, JCA Broen, C P Simeon, L Beretta in Journal of Translational Medicine (2010)

  9. Article

    Open Access

    Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

    In this study we aimed to evaluate the role of a SNP in intron 1 of the ERCC4 gene (rs744154), previously reported to be associated with a reduced risk of breast cancer in the general population, as a breast canc...

    A Osorio, R L Milne, G Pita, P Peterlongo, T Heikkinen in British Journal of Cancer (2009)

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    Article

    Bilateral renal cell carcinoma development in long-term Fabry disease

    D. Cassiman, K. Claes, E. Lerut, R. Oyen in Journal of Inherited Metabolic Disease (2007)

  11. Article

    Open Access

    BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families

    Worldwide variation in the distribution of BRCA1 and BRCA2 mutations is well recognised, and for the Belgian population no comprehensive studies about BRCA1/2 mutation spectra or frequencies have been published. ...

    K Claes, B Poppe, I Coene, A De Paepe, L Messiaen in British Journal of Cancer (2004)

  12. Article

    Open Access

    Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition

    The chromosomal radiosensitivity of breast cancer patients with a known or putative genetic predisposition was investigated and compared to a group of healthy women. The chromosomal radiosensitivity was assess...

    A Baeyens, H Thierens, K Claes, B Poppe, L Messiaen in British Journal of Cancer (2002)

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    Article

    Double Prosthetic Valve Endocarditis Caused by Streptococcus pneumoniae

    K. Claes, F. De Man, F. Van de Werf, W.E. Peetermans in Infection (2000)