Vitamin D Receptor biochemical and genetic profiling and HLA-class II genotyping among Lebanese with multiple sclerosis – A pilot study von Yamout, Bassem, Karaky, Nathalie M, Mahfouz, Rami A.R, Jaber, Fadel, Estaitieh, Nour, Shamaa, Dina, Abbas, Fatmeh, Hoteit, Rouba, Daher, Rose T

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HLA Class I allele frequencies in the Lebanese population von Khansa, Sara, Hoteit, Rouba, Shammaa, Dina, Khalek, Rabab Abdel, El Halas, Hussein, Greige, Layal, Abbas, Fatmeh, Mahfouz, Rami A.R.

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MEFV gene mutations spectrum among Lebanese patients referred for Familial Mediterranean Fever work-up: Experience of a major tertiary care center von Sabbagh, Amira S, Ghasham, Mona, Abdel Khalek, Rabab, Greije, Layal, Shammaa, Dina M. R, Zaatari, Ghazi S, Mahfouz, Rami A. R

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Angiotensin-converting enzyme gene polymorphism and allele frequencies in the lebanese population: prevalence and review of the literature von Sabbagh, Amira S, Otrock, Zaher K, Mahfoud, Ziyad R, Zaatari, Ghazi S, Mahfouz, Rami A. R

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Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study von Mahfouz, Rami A. R., Sarieddine, Doja S., Charafeddine, Khalil M., Abdul Khalik, Rabab N., Cortas, Najwa K., Daher, Rose T.

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Apolipoprotein E gene polymorphism and allele frequencies in the Lebanese population von Mahfouz, Rami A R, Sabbagh, Amira S, Zahed, Laila F, Mahfoud, Ziyad R, Kalmoni, Rana F, Otrock, Zaher K, Taher, Ali T, Zaatari, Ghazi S

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Plasminogen Activator Inhibitor-1 (PAI-1) gene 4G/5G alleles frequency distribution in the Lebanese population von Shammaa, Dina M. R, Sabbagh, Amira S, Taher, Ali T, Zaatari, Ghazi S, Mahfouz, Rami A. R

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Factor XIII gene V34L mutation in the Lebanese population: Another unique feature in this community von Mahfouz, Rami A. R, Sabbagh, Amira S, Shammaa, Dina M. R, Otrock, Zaher K, Zaatari, Ghazi S, Taher, Ali T

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ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature von Sabbagh, Amira S, Daher, Rose T, Otrock, Zaher K, Khalek, Rabab N Abdel, Zaatari, Ghazi S, Mahfouz, Rami A R

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A nationwide non-interventional epidemiological data registry on myelodysplastic syndromes in Lebanon von Otrock, Zaher K, Chamseddine, Nabil, Salem, Ziad M, Wehbe, Tarek, Al-Ayoubi, Mouna, Dhaini, Moussa, Kattan, Joseph, Mokaddem, Walid, Nasr, Therese Abi, Jradi, Oussama, Farhat, Fadi S, Wehbe, Mahmoud, Haidar, Mohammad H, Kharfan-Dabaja, Mohamed A, Bitar, Nizar, Hajj, Mirna El, Kadri, Adel M, Kamar, Francois G, Yassine, Hanan, Khodr, Hassan, Taher, Ali T, Hakime, Noha, Mahfouz, Rami Ar, Serhal, Wassim, Bazarbachi, Ali, Farhat, Hussein Z

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Frequency distribution of the G/A alleles of the b-fibrinogen gene in the Lebanese population von Shammaa, Dina MR, Sabbagh, Amira S, Taher, Ali T, Zaatari, Ghazi S, Mahfouz, Rami AR

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Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome von Otrock, Zaher K, Sharara, Ala I, Mahfouz, Rami AR, Taher, Ali T

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