B Beksac, AGD Valle, EA Salvati - Clinical Orthopaedics & Related Research, 2006 - currentopinion.com Each author certifies that he or she has no commercial associations (eg,
consultancies, stock ownership, equity interest, patent/licensing arrangements,
etc) that might pose a conflict of interest in connection with the ... Cited by 13 - Related articles - Cached - BL Direct - All 5 versions
AS Sabbagh, ZK Otrock, ZR Mahfoud, GS … - Molecular Biology Reports, 2007 - Springer Abstract We studied the distribution of the D/D, I/D, and I/I genotypes of the
angiotensin-converting enzyme (ACE) in a sample of healthy Lebanese indi-
viduals to assess their prevalence and compare them with other populations. ... Cited by 8 - Related articles - BL Direct - All 3 versions
H Köppel, W Renner, A Gugl, L Cichocki, R … - Thrombosis and haemostasis, 2004 - cat.inist.fr The insertion/deletion(I/D) polymorphism of the gene for
angiotensin-converting-enzyme(ACE) is associated with ACE plasma levels and
activity. Conflicting results have been reported about the relevance of ... Cited by 8 - Related articles - BL Direct - All 4 versions
- ►currentopinion.com EA Salvati, NE Sharrock, G Westrich, HG … - Clinical Orthopaedics & Related Research, 2007 - journalpatientsafety.com From the Department of *Orthopaedics, Department of †Anesthesia, and
Department of ‡Radiology, Hospital for Special Surgery and Weill Medical
College of Cornell University, New York, NY. Cited by 5 - Related articles - BL Direct - All 8 versions
- ►leidenuniv.nl [PDF] EP Buddingh, AV Vlieg, FR Rosendaal - Journal of Thrombosis and Haemostasis, 2005 - openaccess.leidenuniv.nl The angiotensin-converting enzyme (ACE) I/D polymorphism is an
insertion/deletion of an ALU-repeat sequence of 287 base pairs (bp) in intron 16
of the ACE gene, located at 17q23. This results in three genotypes: II, ID ... Cited by 4 - Related articles - View as HTML - All 5 versions
DJM Bowler, E Bale, JO'Byrne - Irish Journal of Medical Science, 2007 - Springer Abstract Background The Factor V Leiden (FVL) mutation is the commonest genetic
abnormality associated with venous thromboembolism. Aims To determine the
prevalence of the FVL mutation in Irish patients undergoing total hip ... Cited by 2 - Related articles - BL Direct - All 2 versions
TF Tsai, CH Yang, CY Chu, YH Liou, WC … - Journal of Dermatological Science, 2009 - Elsevier Livedoid vasculopathy (LV) is an idiopathic cutaneous occlusive vasculopathy and
commonly associated with altered procoagulant mechanisms precipitated by several
factors [1]. Polymorphisms in factor V (R506; Leiden), prothrombin (PRT; ... Related articles - All 3 versions
ACE LEVELS, ACEG POLIMORPHISM - Turkish J Vasc Surg, 2006 - uvcd.org.tr Page 1. Turkish J Vasc Surg 2006; 15 (1): 1-6 Dr. Kemal Ayalp ve Arkadafllar›
1 VENÖZ TROMBOEMBOL‹ZM‹N PLAZMA ACE DÜZEYLER‹ VE ACE GEN POL‹MORF‹ZM‹ ILE
‹L‹fiK‹S‹ THE RELATIONSHIP OF VENOUS THROMBOEMBOLISM WITH PLASMA ... Related articles - View as HTML
K Lacut, A Delluc, E Le Moigne, D Mottier - Médecine thérapeutique, 2008 - john-libbey-eurotext.fr Résumé : Une association entre maladie artérielle athéromateuse et maladie
veineuse thromboembolique (MVTE) est évoquée. Des facteurs de risque
artériels classiques pourraient être aussi des facteurs de risque de ... Related articles - All 2 versions
