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Articles by Guy Van Camp
Integrating corneal endophenotypes with classic GWAS approaches identifies novel keratoconus loci
Abstract Keratoconus is a chronic progressive disorder characterized by corneal deformation. It usually affects adolescents and young adults, reducing vision and decreasing the quality of life. Here we show that integrating genetic analyses of corneal traits with large case-control studies improves the discovery and annotation of genetic factors underlying keratoconus.
Response to: Correspondence on “Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics” by José Alberto San Román
Response to: Correspondence on “Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics” by José Alberto San Román Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Response to: Correspondence on “Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics” by José Alberto San Román
http://orcid.org/0000-0002-9815-8337Guy Van Camp1,2 1Cardiology, Onze Lieve Vrouwziekenhuis, Aalst, Belgium 2Cardiology, Hartcentrum OLV Aalst, Aalst, Belgium Correspondence to Professor Guy Van Camp, Cardiology, Onze Lieve Vrouwziekenhuis, Aalst 9300, Belgium; guy_vancamp{at}outlook.com Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service.
Pre-clinical modelling of ROS1+ non-small cell lung cancer
Tessarollo L. Nagarajan L. Parada L.F. c-ros: the vertebrate homolog of the sevenless tyrosine kinase receptor is tightly regulated during organogenesis in mouse embryonic development. Development. 1992; 115: 11-20 Rabin M. Birnbaum D. Young D. Birchmeier C. Wigler M. Ruddle F.H. Human ros1 and mas1 oncogenes located in regions of chromosome 6 associated with tumor-specific rearrangements. Oncogene Res.
UZ Clear Finds 50% Patients with Angina Have Evidence of CAD
- Hello. My name is Carlos Collet. I'm an interventional cardiologist co-director of the Cardiovascular Centre OLV-Aalst in Belgium. Importance of this trial So we have performed a trial where we have included patients with angina, positive exercise tests and an intermediate probability of coronary artery disease. And in those patients, we have studied both the macro or the epicardial circulation and the microcirculation.
Unifying the Cardiology Care Pathway Through a Dedicated Cardiology IT Solution: Helping to Improve Reporting Efficiency in Key Cardiology Disciplines | Radcliffe Cardiology
Views: 3325 Likes: 9 Overview Healthcare professionals (Cardiologists and CIOs) are constantly looking to find ways to unify the cardiology care pathway. In this webinar we discuss how cardiology software solutions can help to achieve this by unifying structured data, images and analysis tools to help generate faster, more informed decisions, and ultimately give time back to the clinicians for them to spend with what matters the most, their patients.
Tumor-specific genetic variants can be detected in circulating cell-free DNA of malignant pleural mesothelioma patients
Publication HistoryPublished online: July 21, 2018Accepted: July 20, 2018; Received in revised form: July 18, 2018; Received: May 11, 2018;
Correction: Whole-Genome Saliva and Blood DNA Methylation Profiling in Individuals with a Respiratory Allergy
There is a typographical error in Table 2. Table 2 reports averaged values of multiple CpG sites in the reported gene regions instead of the average of the single CpG site corresponding to the validated cg-probes. For instance, for cg19754622 in the STK32C gene region (S1 Dataset), the authors reported the average of the 6 CpG sites that were analyzed along with the CpG-site of interest (cg19754622 = CpG1). A similar switch of data for the other two gene regions is also present.
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