A. Abchee

发表

Delay in Seeking Health Care for Acute Coronary Syndromes in a Lebanese Sample

S. Noureddine, M. Arevian, M. Adra, 2006, Journal of transcultural nursing : official journal of the Transcultural Nursing Society.

Endovascular transcatheter aortic valve implantation: an evolving standard.

C. Ayoub, A. Abchee, P. Sfeir, 2013, Journal of cardiothoracic and vascular anesthesia.

Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases

Andreas Massouras, A. Khalil, M. Refaat, 2019, BMC Medical Genomics.

Serum C-Reactive Protein and Complement Proteins in Patients with Acute Myocardial Infarction

Elias A. Rahal, Youssef A. Halas, R. Haddad, 2005, Immunopharmacology and immunotoxicology.

Parental consanguinity and family history of coronary artery disease strongly predict early stenosis.

Samir Alam, D. Platt, P. Zalloua, 2010, Atherosclerosis.

Genetic and environmental influences on total plasma homocysteine and its role in coronary artery disease risk.

Y. Kamatani, D. Gauguier, D. Platt, 2012, Atherosclerosis.

Predictors of coronary artery disease in the Lebanese population.

S. Azar, P. Zalloua, Houry Puzantian, 2006, Thrombosis research.

Artificial neural network-based model enhances risk stratification and reduces non-invasive cardiac stress imaging compared to Diamond–Forrester and Morise risk assessment models: A prospective study

I. Elhajj, W. Jaber, A. Abchee, 2018, Journal of Nuclear Cardiology.

Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy

Ossama K. Abou Hassan, J. Seidman, J. Ware, 2020, Circulation. Genomic and precision medicine.

Association of waterpipe smoking with myocardial infarction and determinants of metabolic syndrome among catheterized patients

D. Platt, P. Zalloua, P. Salameh, 2017, Inhalation toxicology.

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations.

A. Marian, R. Roberts, D. Kelly, 1995, European heart journal.

Sudden cardiac death in hypertrophic cardiomyopathy

A. Marian, R. Roberts, D. Kelly, 1995 .

ALOX5AP gene variants show differential association with coronary artery disease in different populations

G. Khazen, D. Platt, M. El-Sibai, 2010, Journal of Community Genetics.

atients With Early Onset of Type 1 iabetes Have Significantly Higher GG enotype at Position 49 of the TLA 4 Gene ierre

H. Terwedow, A. Abchee, G. Zreik, 2004 .

Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene.

S. Azar, H. Terwedow, P. Zalloua, 2004, Human immunology.

Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature

G. Fuleihan, G. Nemer, A. Abchee, 2018, Osteoporosis International.

Isolated Left Ventricular Diastolic Collapse Due to Extra‐Thoracic Compression

A. Abchee, Jad Zahnan, H. Skouri, 2015, Echocardiography.

Pharmacological therapy for myocardial reperfusion injury.

G. Moukarbel, C. Ayoub, A. Abchee, 2004, Current opinion in pharmacology.

PULMONARY THROMBOEMBOLISM IN β-THALASSEMIA INTERMEDIA: ARE WE AWARE OF THIS COMPLICATION?

A. Shamseddine, A. Taher, A. Abchee, 2002, Hemoglobin.

Coronary Artery Anomalies and Associated Radiologic Findings.

C. Saade, M. Refaat, A. Abchee, 2019, Journal of computer assisted tomography.

The I allele of the angiotensin converting enzyme I/D polymorphism confers protection against coronary artery disease

M. El-Sibai, S. Azar, P. Zalloua, 2010, Coronary artery disease.

Impact of inflammation, gene variants, and cigarette smoking on coronary artery disease risk

G. Khazen, D. Platt, Marc Haber, 2015, Inflammation Research.

Association of hypertension with coronary artery disease onset in the Lebanese population

G. Khazen, D. Gauguier, D. Platt, 2014, SpringerPlus.

Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis

Jean-Baptiste Cazier, Dominique Gauguier, Daniel E. Platt, 2012, PloS one.

Elevated Lp(a) Levels Correlate with Severe and Multiple Coronary Artery Stenotic Lesions

D. Gauguier, D. Platt, P. Zalloua, 2023, Vascular health and risk management.

A new device for easier handling of the transoesophageal echocardiography probe

Chadi I. Yaacoub, M. Rizk, C. Ayoub, 2004, Anaesthesia.

Circulating lipid levels and risk of coronary artery disease in a large group of patients undergoing coronary angiography

Y. Kamatani, G. Khazen, D. Gauguier, 2014, Journal of Thrombosis and Thrombolysis.

Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathies.

R. Krahe, R. Roberts, J. Durand, 1997, Molecular and cellular probes.

Association Between Sedentary Lifestyle and Diastolic Dysfunction Among Outpatients With Normal Left Ventricular Systolic Function Presenting to a Tertiary Referral Center in the Middle East

W. AlJaroudi, A. Abchee, C. Alraies, 2016, Clinical cardiology.

Molecular genetics of familial hypertrophic cardiomyopathy

R. Roberts, A. Abchee, 1996 .

Genome-wide association analysis of HDL-C in a Lebanese cohort

G. Khazen, P. Zalloua, R. Deek, 2019, PloS one.

Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction

D. Platt, P. Zalloua, P. Salameh, 2017, Diabetology & Metabolic Syndrome.

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

J. Towbin, S. Daiger, A. Marian, 1995, Circulation.

Nicotine metabolism in healthy smokers and patients with cardiovascular diseases

P. Zalloua, R. Chahine, A. Abchee, 2005, Molecular and Cellular Biochemistry.

Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population

D. Platt, Marc Haber, P. Zalloua, 2014, Diabetology & Metabolic Syndrome.

Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant

D. Gauguier, D. Platt, Marc Haber, 2015, Annals of Nutrition and Metabolism.

Molecular and clinical aspects of inherited cardiomyopathies.

R. Roberts, J. Durand, R. Roberts, 1995, Annals of medicine.

Prognostic significance of beta-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy.

A. Marian, A. Abchee, 1997, Journal of investigative medicine : the official publication of the American Federation for Clinical Research.

Coronary Computed Tomography: Identification of a Novel Type of Dual Left Anterior Decending Coronary Artery Circulation

C. Saade, W. AlJaroudi, A. Abchee, 2015 .

Prevalence of coronary artery calcium among asymptomatic men and women in a developing country: comparison with the USA data.

A. Mehio-Sibai, Tarek A. Sibai, A. Abchee, 2005, Atherosclerosis.

Prevalence and Predictors of Worsening of Diastolic Function in Cancer Patients with Normal Baseline Ejection Fraction undergoing Chemotherapy

W. AlJaroudi, A. Abchee, H. Skouri, 2014 .

Quantifying the impact of using Coronary Artery Calcium Score for risk categorization instead of Framingham Score or European Heart SCORE in lipid lowering algorithms in a Middle Eastern population

L. Al-Shaar, F. El-Merhi, A. Abchee, 2015, Journal of the Saudi Heart Association.

Association of coronary artery disease and chronic kidney disease in Lebanese population.

G. Khazen, D. Gauguier, D. Platt, 2015, International journal of clinical and experimental medicine.

Homocysteine levels, H-Hypertension, and the MTHFR C677T genotypes: A complex interaction

Xiping Xu, D. Platt, P. Zalloua, 2023, Heliyon.

901–88 Rapid Genetic Screen for Common β-Myosin Heavy Chain Mutations Causing Familial Hypertrophic Cardiomyopathy

R. Roberts, L. Bachinski, G. Greve, 1995 .

Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR 1 as a Major Determinant of Coronary Artery Stenosis

Y. Kamatani, M. Farrall, G. Khazen, 2012 .