Citations (23)
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Aisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, Mohamed Yassin & Hatem Zayed. (2021) The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. Expert Review of Hematology 14:1, pages 109-122.
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Wissem Abdaoui, Djamel Eddine Benouareth, Amel Djenouni, Celine Renoux, Fatiha Grifi, Adel Gouri, Fateh Athamnia, Manel Benalioua & Philippe Joly. (2019) Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15) . Hemoglobin 43:4-5, pages 223-228.
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Awatef Mejri, Marwa Mansri, Sondess Hadj Fredj, Faida Ouali, Amina Bibi, Raouf Hafsia, Taieb Messaoud & Hajer Siala. (2016) First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients. Hemoglobin 40:6, pages 411-416.
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Silvana F. Fonseca, Jose P. Moura Neto & Marilda S. Goncalves. (2013) Prevalence and Molecular Characterization of β-Thalassemia in the State of Bahia, Brazil: First Identification of Mutation HBB: c.135delC in Brazil. Hemoglobin 37:3, pages 285-290.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Imen Moumni, Amine Zorai, Bechir Ben Daoued, Ikbel Mosbahi, Souheil Omar, Neziha Kaabachi, Koussay Dellagi & Salem Abbes. (2007) Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation. Hemoglobin 31:1, pages 23-29.
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Amina Bibi, Taieb Messaoud, Cherif Beldjord & Slaheddine Fattoum. (2006) Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G). Hemoglobin 30:4, pages 437-447.
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Amina Bibi, Taieb Messaoud & Slaheddine Fattoum. (2006) Haplotypes Linked to Three Rare β-Thalassemia Mutations, Originally Reported in Tunisia. Hemoglobin 30:2, pages 175-181.
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Henri Wajcman & Rajagopal Krishnamoorthy. (2004) Thalassemia in Tunisia: More Tasks Ahead. Hemoglobin 28:3, pages 171-172.
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Articles from other publishers (12)
Taher Mahmoud, Chaima Sahli, Sondess Hadj Fredj, Yessine Amri, Rim Othmani, Ghaber S. Mohamed, Ekhtelbenina Zein & Taieb Messaoud. (2022) Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients. Molecular Genetics & Genomic Medicine 10:10.
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Chaima Kasmi, Yessine Amri, Sondess Hadj-Fredj, Sabrine Oueslati, Malek Dabboussi, Rahma Mahjoub, Sana Hammami, Imen Aljane, Faika Ben Mami, Henda Jamoussi, Taieb Messaoud & Amina Bibi. (2021) Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations. Molecular Biology Reports 48:8, pages 5923-5933.
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H. Ben Hamouda, B. Mahjoub, H. Soua, S. Laradi, A. Miled & M.T. Sfar. (2017) Expression néonatale d’un trait bêta-thalassémique associé à une sphérocytose héréditaire chez deux jumelles monozygotes. Archives de Pédiatrie 24:2, pages 126-130.
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Chaima Abdelhafidh Sahli, Ikbel Ben Salem, Latifa Jouini, Naouel Laouini, Rym Dabboubi, Sondes Hadj Fredj, Hajer Siala, Rym Othmeni, Boutheina Dakhlaoui, Slaheddine Fattoum, Amina Bibi & Taieb Messaoud. (2016) Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC). Journal of Clinical Laboratory Analysis 30:5, pages 392-398.
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F. Ouali, H. Siala, A. Bibi, S. Hadj Fredj, B. Dakhlaoui, R. Othmani, F. Ouenniche, F. Zouari, B. Bouguerra, H. Rezigua, S. Fattoum & T. Messaoud. (2016) Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience. International Journal of Laboratory Hematology 38:3, pages 223-232.
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L. Jouini, C. A. Sahli, N. Laaouini, F. Ouali, I. Ben Youssef, B. Dakhlaoui, R. Othmeni, F. Ouennich, S. Hadj Fredj, H. Siala, M. Becher, N. E. Toumi, S. Fattoum, R. Hafsia, A. Bibi & T. Messaoud. (2013) Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients. Molecular Biology Reports 40:11, pages 6205-6212.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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Awatef Mejri, Hajer Siala, Faida Ouali, Amina Bibi & Taieb Messaoud. (2012) Identification of candidate genes involved in clinical variability among Tunisian patients with β-thalassemia. Gene 506:1, pages 166-172.
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Lilia Romdhane & Sonia Abdelhak. (2010) Genetic diseases in the Tunisian population. American Journal of Medical Genetics Part A 155:1, pages 238-267.
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Imed Touhami, Slaheddine Fattoum, Amina Bibi, Hajer Siala, Taieb Messaoud, Donia Koubaa, Rafik Mankai, Zakia Bartagi & Daniel Le Gallais. (2009) The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes. European Journal of Applied Physiology 108:6, pages 1075-1081.
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Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
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