Citations (17)
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Prashant Deshpande, Neelagandan Kamalanathan, Eswari Sampath, Biju George, Ramachandran V. Shaji & Eunice S. Edison. (2015) Characterization of Clinical and Laboratory Profiles of the Deletional α2-Globin Gene Polyadenylation Signal Sequence (AATAAA > AATA– –) in an Indian Population. Hemoglobin 39:6, pages 415-418.
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Maria Elisabetta Paglietti, Maria Carla Sollaino, Daniela Loi, Susanna Barella, Maria Franca Desogus & Renzo Galanello. (2012) First Detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in An Italian Child. Hemoglobin 36:3, pages 299-304.
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Joanne Traeger-Synodinos, Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Vasilis Ladis, Tania Siahanidou, Irine Fylaktou & Emmanuel Kanavakis. (2010) Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Hemoglobin 34:5, pages 430-438.
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Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi, Dimitrios Kampourakis, Amalia Tsilimigaki, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 379-385.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Giuseppina Lacerra, Rosario Testa, Maria De Angioletti, Gino Schilirò & Clementina Carestia. (2003) Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2‐Globin Gene, Associated with a Mild α+‐Thalassemia Phenotype. Hemoglobin 27:3, pages 149-159.
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J. Traeger-Synodinos, A. Metaxotou-Mavrommati, M. Karagiorga, C. Vrettou, I. Papassotiriou, A. Stamoulakatou & E. Kanavakis. (1999) Interaction of an α+-Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-Thalassemia. Hemoglobin 23:4, pages 325-337.
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J. Traeger-Synodinos, A. Metaxotou-Mavromati, E. Kanavakis, C. Vrettou, I. Papassotiriou, Th. Michael & C. Kattamis. (1998) An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain Variant. Hemoglobin 22:3, pages 209-215.
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Articles from other publishers (8)
Ankur Jain, Pooja Prasad, Sumita Chaudhry, D.K. Gupta & Sumita Saluja. (2021) Hb Sun Prairie: A rare cause of chronic hemolysis in an Indian patient. Hematology/Oncology and Stem Cell Therapy 14:3, pages 257-259.
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Giovanna Cardiero, Gennaro Musollino, Maria Grazia Friscia, Rosario Testa, Lucrezia Virruso, Caterina Di Girgenti, Mercedes Caldora, Rosario Colella Bisogno, Carlo Gaudiano, Giuseppe Manco & Giuseppina Lacerra. (2020) Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy. Genes 11:8, pages 870.
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Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Anna Haywood, Helene Dreau, Adele Timbs, Anna Schuh, John Old & Shirley Henderson. (2010) Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing. Annals of Hematology 89:12, pages 1215-1221.
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Cristina Passarello, Antonino Giambona, Luciano Prossomariti, Massimiliano Ammirabile, Piero Pucci, Disma Renda, Leonilde Pagano & Aurelio Maggio. (2008)
Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie α
2
130 Ala → Pro and Hb Caserta α
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26 Ala → Thr) in a single
HBA2
gene
. British Journal of Haematology 143:1, pages 138-142.
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Anjali A. Sarkar, Chaitali Mukhopadhyay, Sharmila Chandra, Subrata Banerjee, M. K. Das & Uma B Dasgupta. (2005) Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population. British Journal of Haematology 129:2, pages 282-286.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes
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Joanne Traeger-Synodinos, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Christina Vrettou, Alexandra Stamoulakatou & Emmanuel Kanavakis. (2000) Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies. Blood Cells, Molecules, and Diseases 26:4, pages 276-284.
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