A novel case of homozygous LDLRAP1 gene mutation causing autosomal recessive familial hypercholesterolemia in Kuwait von Alelaj, K.F.M.F., Alrajhi, N.I., Alsarraf, A.J., Aljarallah, M.A.

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Consensus recommendations for diagnosis and treatment of Multiple Sclerosis: 2023 revision of the MENACTRIMS guidelines von Yamout, B., Al-Jumah, M., Sahraian, M.A., Almalik, Y, Khaburi, J. Al, Shalaby, N., Aljarallah, S, Bohlega, S., Dahdaleh, M., Almahdawi, A., Khoury, S.J., Koussa, S., Slassi, E., Daoudi, S, Aref, H., Mrabet, S., Zeineddine, M., Zakaria, M., Inshasi, J., Gouider, R., Alroughani, R.

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Gene Expression Profiling of Apoptotic Proteins in Circulating Peripheral Blood Mononuclear Cells in Type II Diabetes Mellitus and Modulation by Metformin von Al Dubayee, Mohammed, Alshahrani, Awad, Aljada, Dana, Zahra, Mahmoud, Alotaibi, Ahmed, Ababtain, Ibrahim, Alnaim, Malik, Alahmari, Ali, Aljarallah, Abdullah, Elahi, Muhammad Affan, Fakhoury, Hana M A

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