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André R. Belisário, Anna B. Carneiro-Proietti, Ester Cerdeira Sabino, Aderson Araújo, Paula Loureiro, Cláudia Máximo, Miriam V. Flor-Park, Daniela D.O.W. Rodrigues, Mina Cintho Ozahata, Christopher McClure, Rosimere Afonso Mota, Isabel C. Gomes Moura, Brian Custer & Shannon Kelly. (2020) Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics. Hemoglobin 44:1, pages 1-9.
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Gisele C.S. Carrocini, Larissa P.R. Venancio, Viviani L.R. Pessoa, Clarisse L.C. Lobo & Claudia R. Bonini-Domingos. (2017) Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil. Hemoglobin 41:1, pages 12-15.
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Sandrine C. Wagner, Juliana D. Lindenau, Simone M. de Castro, Ana Paula Santin, Carina F. Zaleski, Laura A. Azevedo, Ândrea K. C. Ribeiro dos Santos, Sidney E.B. dos Santos & Mara H. Hutz. (2016) High Frequency of Hb E-Saskatoon (HBB: c.67G > A) in Brazilians: A New Genetic Origin?. Hemoglobin 40:4, pages 228-230.
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Aylla N. L. M. Silva, Greice L. Cardoso, Daniele A. Cunha, Isabela G. Diniz, Sidney E.B. Santos, Gabriela B. Andrade, Saide M.S. Trindade, Maria do Socorro O. Cardoso, Larissa T.V.M. Francês & João F. Guerreiro. (2016) The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon. Hemoglobin 40:1, pages 20-24.
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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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Martha Bravo-Urquiola, Anabel Arends, Gilberto Gómez, Silvia Montilla, Nathalie Gerard, Marycarmen Chacin, Tsouria Berbar, Odalis García, Gloria García, Dalia Velasquez, Omar Castillo & Rajagopal Krishnamoorthy. (2012) Molecular Spectrum of β-Thalassemia Mutations in the admixed Venezuelan population, and their linkage to β-Globin Gene Haplotypes. Hemoglobin 36:3, pages 209-218.
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Andrea Cristina Fernandes, Marily Maria Azevedo Shimmoto, Gilberto Koiti Furuzawa, Perla Vicari & Maria Stella Figueiredo. (2011) Molecular Analysis of β-Thalassemia Patients: First Identification of Mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil. Hemoglobin 35:4, pages 358-366.
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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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Articles from other publishers (10)
Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Flaviene F. Torres, Victoria S. Bernardo, Danilo G.H. Silva, Jéssika V. Okumura & Claudia R. Bonini-Domingos. (2022) Association of FOXO3 polymorphism (rs3800231) and clinical subphenotypes of beta thalassemic individuals. Hematology, Transfusion and Cell Therapy 44:2, pages 156-162.
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Clóvis Paniz, Maylla Rodrigues Lucena, Juliano Felix Bertinato, Magnun Nueldo Nunes Santos, Guilherme Wataru Gomes, Maria Stella Figueiredo, Maria de Fátima Sonati, Vera Lúcia Nascimento Blaia‐D Avila, Ralph Green & Elvira Maria Guerra‐Shinohara. (2020) Serum folate and cytokines in heterozygous β‐thalassemia. International Journal of Laboratory Hematology 42:6, pages 718-726.
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Camila Cruz de Martino, Cecilia Salete Alencar, Paula Loureiro, Anna Barbara de Freitas Carneiro-Proietti, Claudia de Alvarenga Máximo, Rosimere Afonso Mota, Daniela Oliveira Werneck Rodrigues, Nelson Gaburo Junior, Shannon Kelly & Ester Cerdeira Sabino. (2019) Use of an automated pyrosequencing technique for confirmation of sickle cell disease. PLOS ONE 14:12, pages e0216020.
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Wenguang Jia, Weidong Wang, Hengying Zhu & Ping Chen. (2019) A Novel Mutation at HBB: c.91delA (Codon 30, –A) Causing β-Thalassemia in a Chinese Family. Acta Haematologica 142:4, pages 249-252.
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Marina Neves Ferreira, Claudia Regina Bonini-Domingos, Isabeth Fonseca Estevão, Clarice Lopes de Castro Lobo, Gisele Cristina Souza Carrocini, Aparecida Perpétuo Silveira-Carvalho, Octávio RicciJrJr, Luiz Carlos de Mattos & Cinara Cássia Brandão de Mattos. (2017) Anti-Toxoplasma gondii antibodies in patients with beta-hemoglobinopathies: the first report in the Americas. BMC Research Notes 10:1.
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Zama Messala Luna da Silveira, Maria das Vitórias Barbosa, Thales Allyrio Araújo de Medeiros Fernandes, Elza Miyuki Kimura, Fernando Ferreira Costa, Maria de Fátima Sonati, Ivanise Marina Moretti Rebecchi & Tereza Maria Dantas de Medeiros. (2011) Characterization of beta-thalassemia mutations in patients from the state of Rio Grande do Norte, Brazil. Genetics and Molecular Biology 34:3, pages 425-428.
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Greice De Lemos Cardoso & João Farias Guerreiro. (2010) Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará. American Journal of Human Biology 22:5, pages 573-577.
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Vivian C. D. Reichert, Simone M. de Castro, Sandrine C. Wagner, Dulcinéia M. de Albuquerque, Mara H. Hutz & Sandra Leistner-Segal. (2007) Identification of β thalassemia mutations in South Brazilians. Annals of Hematology 87:5, pages 381-384.
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Tania Regina Tozetto-Mendoza, Paulo Roberto Santos Ferreira, Nilcéia Maria Viviani, Dulcinéia Martins Albuquerque, Ivana Rizzi & João Targino de Araújo. (2005) Camperdown hemoglobin associated with beta° thalassemia in a Brazilian child. Genetics and Molecular Biology 28:3, pages 394-396.
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