Citations (23)
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Sedat Yılmaz. (2019) The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Hemoglobin 43:3, pages 174-181.
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M. Yousuf Yassouf, Faizeh Alquobaili, Younes Kabalan & Yasser Mukhalalaty. (2019) Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria. Hemoglobin 43:3, pages 218-221.
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Hossam Murad, Faten Moassas, Bashar Ali & Walid Alachkar. (2019) A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report. Cogent Medicine 6:1.
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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Faten Moassas, Ayman Alabloog & Hossam Murad. (2018) Description of a Rare β-Globin Gene Mutation: –86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family. Hemoglobin 42:3, pages 203-205.
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Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty & Walid Al-Achkar. (2014) Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population. Hemoglobin 38:6, pages 390-393.
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Articles from other publishers (15)
Kenneth Oshiokhayamhe Iyevhobu, Omolumen Lucky E.Tobechukwu Joseph Okobi, Edidiong Raphael Usoro, A. Airefetalor Ivie, Benedicta A. Ken-Iyevhobu & O. Omokpo Victoria. 2023. Thalassemia Syndromes - New Insights and Transfusion Modalities. Thalassemia Syndromes - New Insights and Transfusion Modalities.
Dilek Gurlek Gokcebay, Serhan Küpeli, Orhan Gürsel, Ozlem Arman Bilir, Arzu Akyay, Esra Pekpak, Sinan Akbayram, Yurday Öncül, Adalet Meral Güneş, Serap Kirkiz, Suar Çakı Kılıç, İkbal Ok Bozkaya & Namık Yasar Ozbek. (2022) Hematopoietic stem cell transplantation activities and HRQOL of refugee or asylum seeker children in Turkey: A multicenter study. Pediatric Transplantation 26:8.
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Ramazan DULKADİR & Filiz TUBAŞ. (2022) Çocuk Sağlığı ve Hastalıkları Servisine Yatış Yapılan Mülteci Hastaların Sosyo-Demografik, Klinik ve Laboratuvar Özelliklerinin Değerlendirilmesi. Ahi Evran Medical Journal.
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Ahmet Kursad Gunes & Hilmi Erdem Gozden. (2021) The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens. Cureus.
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Hossam Murad, Faten Moassas & Nour A. L. Fakseh. (2021) A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family. Molecular Genetics & Genomic Medicine 9:3.
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Tang-Her Jaing, Tsung-Yen Chang, Shih-Hsiang Chen, Chen-Wei Lin, Yu-Chuan Wen & Chia-Chi Chiu. (2021) Molecular genetics of β-thalassemia. Medicine 100:45, pages e27522.
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Lina Hamad, Khalil Kreidieh, Mirna Bou Hamdan, Ghunwa Nakouzi & Soha Yazbek. (2020) Mapping the Diverse Genetic Disorders and Rare Diseases Among the Syrian Population: Implications on Refugee Health and Health Services in Host Countries. Journal of Immigrant and Minority Health 22:6, pages 1347-1367.
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Rashail Faraon, Mahmoud Daraghmah, Fekri Samarah & Mahmoud A. Srour. (2019) Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine. BMC Hematology 19:1.
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Atyaf S Almousawi & Intisar Razzaq Sharba. (2019) Erythroferrone Hormone a Novel Biomarker is associated with Anemia and Iron Overload in Beta Thalassemia Patients.. Journal of Physics: Conference Series 1294:6, pages 062045.
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Arzu Yazal Erdem, Fatma Demir Yenigürbüz, Esra Pekpak, Burcu Akıncı, Elif Aktekin, Cengiz Bayram, Zeynep Yıldız Yıldırmak, Eda Ataseven, Sinan Akbayram, İlgen Şaşmaz, Başak Taburoğlu Yılmaz, Ayşe Özkan, Sibel Akpınar Tekgündüz, Doğan Köse, Tuba Karapınar, Mustafa Büyükavcı, Ertan Sal, Turan Bayhan, Serap Kirkiz, Şule Ünal, Raziye Canan Vergin, Metin Çil, Barış Malbora, Ali Ayçiçek, Hüsniye Neşe Yaralı & Namık Yaşar Özbek. (2019) Refugee children with beta‐thalassemia in Turkey: Overview of demographic, socioeconomic, and medical characteristics. Pediatric Blood & Cancer 66:5, pages e27636.
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Hatice Çevirici, Can Acıpayam, Ebru Dündar Yenilmez, Fatma Burcu Belen, Esra Pekpak, Yöntem Yaman & Abdullah Tuli. (2019) Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major. Turkish Journal of Biochemistry 44:2, pages 126-129.
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Richard Coffey & Tomas Ganz. (2018) Erythroferrone: An Erythroid Regulator of Hepcidin and Iron Metabolism. HemaSphere 2:2, pages e35.
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Rami A. Jarjour & Rami Abou Jamra. (2017) Mutations of familial Mediterranean fever in Syrian patients and controls: Evidence for high carrier rate. Gene Reports 6, pages 87-92.
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Chi-Kong Li. (2017) New trend in the epidemiology of thalassaemia. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 16-26.
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Ahmad N. Hasan & Mustafa S. Al-Attar. Molecular investigations of β-thalassemic children in Erbil governorate. Molecular investigations of β-thalassemic children in Erbil governorate.