Flow cytometry assessment of monocyte subsets alteration in hepatocellular carcinoma post hepatitis C virus infection von Ali, Fatma, Kotb, Fatma, Aglan, Reda, Alrayes, Mona

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Serum Tryptase and Sputum Cellular Profile in Relation to Asthma Severity von Fouda, Ghada E, Galal, Magd M, Alrayes, Mona H, Fouda, El-Desouki E., MD, FAAAAI

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Circulating Endothelial and Platelet Microparticles For Diagnosis and Monitoring Vasculitis von Fouda, El-Desouki E., Prof, Ahmed, Marwa, Dr, Alrayes, Mona, Prof

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Leukocyte-associated immunoglobulin-like receptor-1, T-cell leukemia/lymphoma protein-1, and nuclear factor κB expression in childhood acute lymphoblastic leukemia von Alrayes, Mona, Hammad, Reham, Farweez, Botheina, Elsherif, Nayera, Aly, Doaa

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Telomere length in chronic obstructive pulmonary disease von Magd, Galal-Eldin M., Entesar, Ahmad S., Manal, Hafez R., Eman, Sobh M., Mona, Alrayes H.

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Leukocyte-associated immunoglobulin-like receptor-1, T-cell leukemia/lymphoma protein-1, and nuclear factor [kappa]B expression in childhood acute lymphoblastic leukemia von Alrayes, Mona, Hammad, Reham, Farweez, Botheina, Elsherif, Nayera, Aly, Doaa

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Clinical Significance of Leukocyte-Associated Immunoglobulin-Like Receptor-1, T-Cell Leukemia/Lymphoma Protein 1 and Nuclear Factor-ҡB in Childhood Acute Lymphoblastic Leukemia von Yousef Alrayes, Mona Hilmy, Mahmoud Hammad, Reham Hammad, Thabet Farweez, Botheina Ahmed, Khalil Elsherif, Nayera Hazaa, Abd El-fattah Aly, Doaa Aly

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Angiogenic and FLT3 Receptors Expression in Acute Lymphoblastic Leukemia in Pediatric Age Group von Alrayes, Mona Hilmy, Hammad, Reham, Baddiny, Mohamed Abd Alazim Hussein EL, Ibrahim, Maha Saleh Madbouly, Hammad, Mahmoud

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A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features von Mohamoud, Hussein Sheikh, Ahmed, Saleem, Jelani, Musharraf, Alrayes, Nuha, Childs, Kay, Vadgama, Nirmal, Almramhi, Mona Mohammad, Al-Aama, Jumana Yousuf, Goodbourn, Steve, Nasir, Jamal

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Consensus on diagnosis and management of Hereditary Angioedema in the Middle East: A Delphi initiative von Maurer, Marcus, Abuzakouk, Mohamed, Al-Ahmad, Mona, Al-Herz, Waleed, Alrayes, Hassan, Al-Tamemi, Salem, Arnaout, Rand, Binghadeer, Hend, Gutta, Ravi, Irani, Carla, Mobayed, Hassan, Nasr, Iman, Shendi, Hiba, Zaitoun, Fares

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Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3 von Ahmed, Saleem, Jelani, Musharraf, Alrayes, Nuha, Mohamoud, Hussein Sheikh Ali, Almramhi, Mona Mohammad, Anshasi, Wasim, Ahmed, Naushad Ali Basheer, Wang, Jun, Nasir, Jamal, Al-Aama, Jumana Yousuf

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Diagnosis and management of osteoporosis in Saudi Arabia: 2023 key updates from the Saudi Osteoporosis Society von Al-Saleh, Yousef, Sulimani, Riad, Sabico, Shaun, Alshahrani, Fahad M., Fouda, Mona A., Almohaya, Mohammed, Alaidarous, Salwa B., Alkhawashki, Hazem M., Alshaker, Mohammed, Alrayes, Hanan, Saleh, Najla, Al-Daghri, Nasser M.

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Incidence of hip fracture in Saudi Arabia and the development of a FRAX model von Saleh, Yousef A. L., Sulimani, Riad A., Alomary, Shaker, Alnajjar, Yassmeen I., Vandenput, Liesbeth, Liu, Enwu, Lorentzon, Mattias, Harvey, Nicholas C., McCloskey, Eugene V., Johansson, Helena, Kanis, John A.

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The alkylglycerol monooxygenase ( AGMO ) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family von Alrayes, Nuha, Mohamoud, Hussein Sheikh Ali, Ahmed, Saleem, Almramhi, Mona Mohammad, Shuaib, Taghreed Mohammad, Wang, Jun, Al-Aama, Jumana Yousuf, Everett, Kate, Nasir, Jamal, Jelani, Musharraf

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