Genetic Variants in PHACTR1 & LPL Mediate Restenosis Risk in Coronary Artery Patients von Al Hageh, Cynthia, Chacar, Stephanie, Venkatachalam, Thenmozhi, Gauguier, Dominique, Abchee, Antoine, Chammas, Elie, Hamdan, Hamdan, O'Sullivan, Siobhan, Zalloua, Pierre, Nader, Moni

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Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature von Chakhtoura, M., Ramnitz, M.S., Khoury, N., Nemer, G., Shabb, N., Abchee, A., Berberi, A., Hourani, M., Collins, M., Ichikawa, S., El Hajj Fuleihan, G.

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Elevated Lp(a) Levels Correlate with Severe and Multiple Coronary Artery Stenotic Lesions von Al Hageh, Cynthia, Chacar, Stephanie, Ghassibe-Sabbagh, Michella, Platt, Daniel E, Henschel, Andreas, Hamdan, Hamdan, Gauguier, Dominique, El Murr, Yara, Alefishat, Eman, Chammas, Elie, O'Sullivan, Siobhán, Abchee, Antoine, Nader, Moni, Zalloua, Pierre A

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Quantification of epi- and pericardial adipose tissue deposits between males and females during cardiac CT may potentially help categorize coronary artery disease risk with thoraci... von El-Merhi, F., Ghieh, D., Taleb, H., Abchee, A., Karout, L., Saade, C.

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Author response to letter to editor. Re: Quantification of epi- and pericardial adipose tissue deposits between males and females during cardiac CT may potentially help categorize... von El Merhi, F., Ghieh, D., Taleb, H., Abchee, A., Karout, L., Tamim, H., Makki, M., Saade, C.

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Severe aortic insufficiency in a patient with sinus of Valsalva aneurysm invading the interventricular septum von Moukarbel, G V, Abchee, A B

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Sudden cardiac death in hypertrophic cardiomyopathy : variability in phenotypic expression of β-myosin heavy chain mutations von MARIAN, A. J, MARES, A. JR, KELLY, D. P, YU, Q.-T, ABCHEE, A. B, HILL, R, ROBERTS, R

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Prevalence of coronary artery calcium among asymptomatic men and women in a developing country: Comparison with the USA data von Dakik, Habib A., Skouri, Hadi N., Mehio-Sibai, Abla, Sibai, Tarek, Alam, Samir, Sawaya, Jaber, Nasrallah, Antoine, Wehbeh, Chadi, Ayach, Kamal, Abchee, Antoine B.

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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32 von DURAND, J.-B, BACHINSKI, L. L, BRUGADA, R, DAIGER, S, GREGORITCH, J. M, ANDERSON, J. L, QUINONES, M, TOWBIN, J. A, ROBERTS, R, BIELING, L. C, CZERNUSZEWICZ, G. Z, ABCHEE, A. B, QUN TAO YU, TAPSCOTT, T, HILL, R, IFEGWU, J, MARIAN, A. J

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A new device for easier handling of the transoesophageal echocardiography probe von Abchee, A. B., Yaacoub, C. I., Rizk, M. S., Ayoub, C. M.

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Molecular and Clinical Aspects of Inherited Cardiomyopathies von Durand, Jean-Bernard, Abchee, Antoine B., Roberts, Robert

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Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene von Zalloua, Pierre A., Abchee, Antoine, Shbaklo, Hadia, Zreik, Tony G., Terwedow, Henry, Halaby, Georges, Azar, Sami T.

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Nicotine metabolism in healthy smokers and patients with cardiovascular diseases von Chahine, Ramez, Abchee, Antoine, Zalloua, Pierre

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Predictors of coronary artery disease in the Lebanese population von Abchee, Antoine, Puzantian, Houry, Azar, Sami T., Shbaklo, Hadia, Nasrallah, Antoine, Sawaya, Fadi J., Alam, Samir, Zalloua, Pierre A.

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Founder mutation in N-terminus of cardiac troponin I causes malignant hypertrophic cardiomyopathy von Fahed, AC, Nemer, G, Bitar, FF, Arnaout, S, Abchee, AB, Batrawi, M, Khalil, A, Abou-Hassan, O, DePalma, SR, McDonough, B, Arabi, MT, Ware, JS, Seidman, JG, Seidman, CE

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Pharmacological therapy for myocardial reperfusion injury von Moukarbel, George V, Ayoub, Chakib M, Abchee, Antoine B

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PULMONARY THROMBOEMBOLISM IN β-THALASSEMIA INTERMEDIA: ARE WE AWARE OF THIS COMPLICATION? von Taher, Ali, Abou-Mourad, Yasser, Abchee, Antoine, Zalouaa, Pierre, Shamseddine, Ali

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Serum C-Reactive Protein and Complement Proteins in Patients with Acute Myocardial Infarction von Halas, Youssef A., Rahal, Elias, Abdelnoor, Alexander M., Haddad, Raja, Abchee, Antoine

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Sudden cardiac death in hypertrophic cardiomyopathy von Marian, A. J., Mares, A., KELLY, D. P., Yu, Q.-T., Abchee, A. B., Hill, R., Roberts, R.

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Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathies von Bachinski, L L, Abchee, A, Durand, J B, Roberts, R, Krahe, R, Hobson, G M

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