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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue sup1
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PROCEEDINGS OF THE 1ST PAN-MIDDLE EASTERN CONFERENCE ON HAEMOGLOBINOPATHIES DAMASCUS (SYRIA), 1–2 MAY, 2009 GUEST EDITORS: MICHAEL ANGASTINIOTIS AND ANDROULLA ELEFTHERIOUThe First Section: Prevention of Haemoglobin Disorders

Steps Toward the Prevention of Hemoglobinopathies in the Kingdom of Saudi Arabia

Pages S21-S24 | Published online: 13 Dec 2009

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Lubna Ibrahim Al Asoom, Marwah Mansour Al Makhaita, Nazish Rafique, Dina Tariq Al Afandi, Waad Mohammed Al Otaibi, Hind Saleh Alsuwat, Mousa A Alaithan, Sayed AbdulAzeez & J Francis Borgio. (2020) Effects of –3.7α Deletion and Sickle-Cell Trait on Ventilatory and Hemodynamic Responses to Maximum Exercise in Young Saudi Females. Journal of Blood Medicine 11, pages 371-378.
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Mohammed Shakil Akhtar, Fuad Qaw, J. Francis Borgio, Waleed Albuali, Ahmed Suliman, Zaki Nasserullah, Sana Al-Jarrash & Amein Al-Ali. (2013) Spectrum of α-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia. Hemoglobin 37:1, pages 65-73.
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Aisha A. Galadanci, Jeremie H. Estepp, Hamda Khan, Zubaida L. Farouk, Yvonne Caroll, Jason Hodges, Sabiu Yarima, Umma A. Ibrahim, Ibrahim M. Idris, Awwal Gambo, Nafiu Hussaini, Aisha Mukaddas, Michael R. DeBaun & Najibah A. Galadanci. (2023) Barriers and Facilitators of Premarital Genetic Counseling for Sickle Cell Disease in Northern Nigeria. Journal of Pediatric Hematology/Oncology 45:6, pages e716-e722.
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Heba M. Al-Qattan, Dana F. Amlih, Fatima S. Sirajuddin, Dalal I. Alhuzaimi, Mai S. Alageel, Reema M. Bin Tuwaim & Farjah H. Al Qahtani. (2019) Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults. Advances in Hematology 2019, pages 1-7.
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J. Borgio, Sayed Abdulazeez, Noor Almandil, Zaki Naserullah, Sana Al‑Jarrash, Ahmed Al‑Suliman, Huda Elfakharay, Fuad Qaw, Fatimah Alabdrabalnabi, Mohammed Alkhalifah, Mohammed Shakil Akhtar, Hatem Qutub & Amein Al‑Ali. (2017) The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population. Molecular Medicine Reports.
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J. Francis Borgio, S. AbdulAzeez, Awatif N. Al-Nafie, Zaki A. Naserullah, Sana Al-Jarrash, Mohammed S. Al-Madan, Fahad Al-Muhanna, Martin H. Steinberg & Amein K. Al-Ali. (2014) A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population. Blood Cells, Molecules, and Diseases 53:4, pages 199-203.
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Satish Chandrasekhar Nair, Halah Ibrahim & David D. Celentano. (2013) Clinical trials in the Middle East and North Africa (MENA) Region: Grandstanding or Grandeur?. Contemporary Clinical Trials 36:2, pages 704-710.
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Ziad Ahmed Memish & Mohammad Y. Saeedi. (2011) Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia. Annals of Saudi Medicine 31:3, pages 229-235.
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Ziad A. Memish, Tariq M. Owaidah & Mohamad Y. Saeedi. (2011) Marked regional variations in the prevalence of sickle cell disease and β-thalassemia in Saudi Arabia: Findings from the premarital screening and genetic counseling program. Journal of Epidemiology and Global Health 1:1, pages 61.
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