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Hemoglobin
international journal for hemoglobin research
Volume 36, 2012 - Issue 3
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Short Communication

First Detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in An Italian Child

Maria Elisabetta PagliettiClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, Italia
,
Maria Carla SollainoClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, Italia
,
Daniela LoiClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, Italia
,
Susanna BarellaClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, Italia
,
Maria Franca DesogusClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, Italia
&
Renzo GalanelloClinica Pediatrica 2°, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Ospedale Regionale Microcitemie, ASL 8 Cagliari, ItaliaCorrespondence[email protected]
Pages 299-304 | Received 14 Nov 2011, Accepted 22 Dec 2011, Published online: 19 Mar 2012

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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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Articles from other publishers (3)

Corinne Vasseur, Elisa Domingues-Hamdi, Katia Ledudal, Philippe Le Corvoisier, Caroline Barau, Bijan Ghaleh, Amandine Rialland, Serge Pissard, Frédéric Galactéros & Véronique Baudin-Creuza. (2017) Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study. British Journal of Haematology 179:1, pages 142-153.
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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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Raffaella Origa, Maria E. Paglietti, Maria C. Sollaino, Maria F. Desogus, Susanna Barella, Daniela Loi & Renzo Galanello. (2014) Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia. Blood Cells, Molecules, and Diseases 52:1, pages 46-49.
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