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Hemoglobin
international journal for hemoglobin research
Volume 32, 2008 - Issue 4
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Original

First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations

Varvara Douna Hematology Laboratory, “P. and A. Kyriakou” Children's Hospital, Athens, Greece
,
Dimitra Liapi Hematology Department, Venizelio-Pananio General Hospital, Heraklion, Greece
,
Dimitrios Kampourakis Pediatric Clinic, Agios Nikolaos General Hospital, Agios Nikolaos, Greece
,
Zoe Repapinou Hematology Laboratory, Heraklion University Hospital, Heraklion, Greece
,
Ioannis Papassotiriou Department of Clinical Biochemistry, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Alexandra Stamoulakatou Hematology Laboratory, “Aghia Sophia” Children's Hospital, Athens, Greece
,
Christos Poziopoulos Hematology Department, 401 Military Hospital, Athens, Greece
,
Emmanuel Kanavakis Laboratory of Medical Genetics, “Aghia Sophia” Children's Hospital, Athens, Greece
&
Joanne Traeger-Synodinos Laboratory of Medical Genetics, “Aghia Sophia” Children's Hospital, Athens, GreeceCorrespondence[email protected]
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Pages 371-378 | Received 15 Jan 2008, Accepted 25 Jan 2008, Published online: 07 Jul 2009

Citations (8)

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Quentin A Hill, Lisa Farrar, Jim Lordan, Alice Gallienne & Shirley Henderson. (2015) A combination of two novel alpha globin variants Hb Bridlington (HBA1) and Hb Taybe (HBA2) resulting in severe hemolysis, pulmonary hypertension, and death. Hematology 20:1, pages 50-52.
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Maja Bech Juul, Hanne Vestergaard, Jesper Petersen & Henrik Frederiksen. (2012) Thrombosis in Hb Taybe [codons 38/39 (–ACC) (α1)]. Hemoglobin 36:6, pages 600-604.
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Yin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou & Dong-Zhi Li. (2012) A Novel Case of Hb Phnom Penh: Codons 117/118 (+ATC) as a Cause of α+-Thalassemia. Hemoglobin 36:3, pages 289-292.
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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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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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Articles from other publishers (2)

Ariel Koren, Carina Levin, Luci Zalman, Haya Palmor, Dvora Filon, Evgeny Chubar, Peretz Resnitzky & Michael Bennett. (2016) Hb TAYBE: clinical and morphological findings IN 43 patients. European Journal of Haematology 97:2, pages 137-144.
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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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