Search Results - "Suliman, Ahmed M"

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

“…Allogeneic HSCT is the only curative treatment for SCD. In this study, we estimated the number of Saudi patients with SCD who are candidates for HSCT. We used…”
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Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype by 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

“…Sickle cell anemia is common in the Middle East and India where the HbS gene is sometimes associated with the Arab-Indian (AI) β-globin gene (HBB) cluster…”
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Implant impression accuracy of parallel and non-parallel implants: a comparative in-vitro analysis of open and closed tray techniques by Osman, Motaz S., Ziada, Hassan M., Abubakr, Neamat H., Suliman, Ahmed M.

“…Background The outcome of the evaluation of impression techniques accuracy may improve the selection criteria for an ideal technique. The aim was to evaluate…”
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Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease by Alsultan, Abdulrahman, Al-Suliman, Ahmed M, Aleem, Aamer, AlGahtani, Farjah H, Alfadhel, Majid

“…Sickle cell disease (SCD) is a monogenic disease that has wide variety of phenotypes with both and environmental factors contributing to its severity. We…”
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Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients by AbdulAzeez, Sayed, Almandil, Noor B., Naserullah, Zaki A., Al-Jarrash, Sana, Al-Suliman, Ahmed M., ElFakharay, Huda I., Borgio, J. Francis

“…In the Eastern province of Saudi Arabia, thalassemia is highly common. Data on the effect of alpha globin gene variation on the concentration of iron on…”
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KLF1 gene and borderline hemoglobin A2 in Saudi population by 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.

“…Introduction: Elevated HbA2 (hemoglobin A2) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However,…”
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Expression of cyclin D1 in oral squamous cell carcinoma by Ahmad, Malak Abd al-Rahman Sayyid, Umar, Nazik, Sulayman, Ahmad M., al-Laythi, Muna

“…Background: Cyclin D1 expression regulates normal cell cycle. Its deregulation or overexpression may cause disruption in the normal cell cycle control and lead…”
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Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients by 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.

“…α-thalassemia X-linked mental retardation syndrome is a rare inherited intellectual disability disorder due to mutations in the ATRX gene. In our previous…”
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A Lady with Severe Abdominal Pain Following a Zumba Dance Session: A Rare Presentation of Bochdalek Hernia by Rehman, Abdul, Maliyakkal, Abdul Majeed, Naushad, Vamanjore A, Allam, Hisham, Suliman, Ahmed M

“…A Bochdalek hernia is a congenital diaphragmatic hernia that results from a failure of closure of the pleuroperitoneal folds during embryologic development…”
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Acute Appendicitis Presenting as an Abdominal Wall Abscess: A Case Report by Ahmed, Khalid, Hakim, Suhail, Suliman, Ahmed M, Aleter, Ammar, El-Menyar, Ayman, Mustafa, Sheriff abdulazeim, Zarour, Ahmad, Al-Thani, Hassan

“…Highlights • Amyand’s hernia is uncommon in females. • The initial presentation as an abdominal wall abscess is very rare in the contemporary literature. • An…”
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Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-[beta]0 thalassemia by 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 by 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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Management of adult immune thrombocytopenia: Recommendations by an expert Saudi panel by Hazzaa Al-Zahrani, Aamer Aleem, Fahad Al Mohareb, Said Yousuf Ahmed, Ahmed M Al-Suliman, Hussain H Al Saeed, Mubarak S Al-Ghamdi, Hani Al-Hashmi

“…Immune thrombocytopenia (ITP) is a disorder characterized by an isolated thrombocytopenia in the absence of an identifiable cause. Management of ITP patients…”
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KLF1 gene and borderline hemoglobin A 2 in Saudi population by 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

“…Elevated HbA (hemoglobin A ) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However, some carriers…”
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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 by 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

“…The regions of Al-Qatif and Al-Ahssa in the Eastern Province of Saudi Arabia are known for their high prevalence of hemoglobinopathies, including…”
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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 by 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

“…The regions of Al‑Qatif and Al‑Ahssa in the Eastern Province of Saudi Arabia are known for their high prevalence of hemoglobinopathies, including β‑thalassemia…”
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The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia by 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

“…High white blood cell (WBC) count is an indicator of sickle cell disease (SCD) severity, however, there are limited studies on WBC counts in Saudi Arabian…”
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Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β 0 thalassemia by 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‐β0 thalassemia by 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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Rapid, Detergent-Free Method for Creation of Acellular Nerve Allografts by Leach, Garrison, Llaneras, Jason, Suliman, Ahmed, Shah, Sameer

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