Demands and challenges for patients with sickle-cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia von Alsultan, Abdulrahman, Jastaniah, Wasil, Al Afghani, Sameera, Al Bagshi, Muneer H., Nasserullah, Zaki, Al-Suliman, Ahmed M., Alabdulaali, Mohammed K.

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Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype von Ngo, Duyen, Bae, Harold, Steinberg, Martin H., Sebastiani, Paola, Solovieff, Nadia, Baldwin, Clinton T., Melista, Efthymia, Safaya, Surinder, Farrer, Lindsay A., Al-Suliman, Ahmed M., Albuali, Waleed H., Al Bagshi, Muneer H., Naserullah, Zaki, Akinsheye, Idowu, Gallagher, Patrick, Luo, Hong-yuan, Chui, David H.K., Farrell, John J., Al-Ali, Amein K., Alsultan, Abdulrahman

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Implant impression accuracy of parallel and non-parallel implants: a comparative in-vitro analysis of open and closed tray techniques von Osman, Motaz S., Ziada, Hassan M., Abubakr, Neamat H., Suliman, Ahmed M.

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Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease von Alsultan, Abdulrahman, Al-Suliman, Ahmed M, Aleem, Aamer, AlGahtani, Farjah H, Alfadhel, Majid

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Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients von AbdulAzeez, Sayed, Almandil, Noor B., Naserullah, Zaki A., Al-Jarrash, Sana, Al-Suliman, Ahmed M., ElFakharay, Huda I., Borgio, J. Francis

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KLF1 gene and borderline hemoglobin A2 in Saudi population von Borgio, J. Francis, AbdulAzeez, Sayed, Al-Muslami, Ahmed M., Naserullah, Zaki A., Al-Jarrash, Sana, Al-Suliman, Ahmed M., Al-Madan, Mohammed S., Al-Ali, Amein K.

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Expression of cyclin D1 in oral squamous cell carcinoma von Ahmad, Malak Abd al-Rahman Sayyid, Umar, Nazik, Sulayman, Ahmad M., al-Laythi, Muna

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Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients von Al-Nafie, Awatif N., Borgio, J. Francis, AbdulAzeez, Sayed, Al-Suliman, Ahmed M., Qaw, Fuad S., Naserullah, Zaki A., Al-Jarrash, Sana, Al-Madan, Mohammed S., Al-Ali, Rudaynah A., AlKhalifah, Mohammed A., Al-Muhanna, Fahad, Steinberg, Martin H., Al-Ali, Amein K.

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A Lady with Severe Abdominal Pain Following a Zumba Dance Session: A Rare Presentation of Bochdalek Hernia von Rehman, Abdul, Maliyakkal, Abdul Majeed, Naushad, Vamanjore A, Allam, Hisham, Suliman, Ahmed M

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Acute Appendicitis Presenting as an Abdominal Wall Abscess: A Case Report von Ahmed, Khalid, Hakim, Suhail, Suliman, Ahmed M, Aleter, Ammar, El-Menyar, Ayman, Mustafa, Sheriff abdulazeim, Zarour, Ahmad, Al-Thani, Hassan

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Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-[beta]0 thalassemia von Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T, Melista, Efthymia, Suliman, Ahmed M, Albuali, Waleed H, Nasserullah, Zaki, Luo, Hong-yuan, Chui, David H.K, Steinberg, Martin H, Al-Ali, Amein K

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Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia von Alsultan, Abdulrahman, Ngo, Duyen, Bae, Harold, Sebastiani, Paola, Baldwin, Clinton T, Melista, Efthymia, Suliman, Ahmed M, Albuali, Waleed H, Nasserullah, Zaki, Luo, Hong-Yuan, Chui, David H K, Steinberg, Martin H, Al-Ali, Amein K

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The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia von Ahmed, Anwar E, Ali, Yosra Z, Al-Suliman, Ahmad M, Albagshi, Jafar M, Al Salamah, Majid, Elsayid, Mohieldin, Alanazi, Wala R, Ahmed, Rayan A, McClish, Donna K, Al-Jahdali, Hamdan

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Rapid, Detergent-Free Method for Creation of Acellular Nerve Allografts von Leach, Garrison, Llaneras, Jason, Suliman, Ahmed, Shah, Sameer

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KLF1 gene and borderline hemoglobin A 2 in Saudi population von Borgio, J Francis, AbdulAzeez, Sayed, Al-Muslami, Ahmed M, Naserullah, Zaki A, Al-Jarrash, Sana, Al-Suliman, Ahmed M, Al-Madan, Mohammed S, Al-Ali, Amein K

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Prophylactic balloon occlusion of the internal iliac arteries to treat abnormal placentation: a cautionary case von Greenberg, Joshua I., MD, Suliman, Ahmed, MD, Iranpour, Pooya, MS, Angle, Niren, MD, RVT, FACS

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Symptoms and Signs of Heart Failure at Admission and Discharge and Outcomes in the Sub-Saharan Acute Heart Failure (THESUS-HF) Registry von Sani, Mahmoud U., MBBS, FWACP, FACP, FACC, Cotter, Gad, MD, FACC, FESC, Davison, Beth A., PhD, Mayosi, Bongani M., DPhil, FCP(SA), Damasceno, Albertino, MD, PhD, FESC, Edwards, Christopher, BS, Ogah, Okechukwu S., MBBS, FWACP, FACC, FESC, Mondo, Charles, MBChB, PhD, Dzudie, Anastase, MD, FESC, Ojji, Dike B., MBBS, PhD, FACP, Kouam Kouam, Charles, MD, Suliman, Ahmed, MD, Yonga, Gerald, MD, Abdou Ba, Sergine, MD, PhD, Maru, Fikru, MD, Alemayehu, Bekele, MD, Sliwa, Karen, MD, PhD, FESC, FACC

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Management of Plastic Surgery Complications at a Tertiary Medical Center after Aesthetic Procedures von Belza, Caitlyn C, Lopes, Kelli, Benyamein, Paige, Harfouche, Cyril, Dean, Riley, Geter, Santaria, Lee, Clara J, Neubauer, Dan, Reid, Chris M, Suliman, Ahmed, Gosman, Amanda A

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The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population von Borgio, J Francis, Abdulazeez, Sayed, Almandil, Noor B, Naserullah, Zaki A, Al-Jarrash, Sana, Al-Suliman, Ahmed M, Elfakharay, Huda Ismail, Qaw, Fuad S, Alabdrabalnabi, Fatimah I, Alkhalifah, Mohammed A, Shakil Akhtar, Mohammed, Qutub, Hatem, Al-Ali, Amein K

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The -[[alpha].sup.3.7] deletion in [alpha]-globin genes increases the concentration of fetal hemoglobin and hemoglobin [A.sub.2] in a Saudi Arabian population von Borgio, J. Francis, Abdulazeez, Sayed, Almandil, Noor B, Naserullah, Zaki A, Al-Jarrash, Sana, Al-Suliman, Ahmed M, Elfakharay, Huda Ismail, Qaw, Fuad S, Alabdrabalnabi, Fatimah I, Alkhalifah, Mohammed A, Akhtar, Mohammed Shakil, Qutub, Hatem, Al-Ali, Amein K

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