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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 5
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Original Article

Is Hb A2 Elevated in Adults with Sickle-A-Thalassemi (βS/βS; -α/-α)

S. K. Ballas Department of Medicine, Cardeza Foundation Jefferson Medical College, Philadelphia, PA, 19107, USA
,
R. N. Gay Sickle Cell Program, Misericordia Hospital, Philadelphia, PA, 19143, USA
&
F. F. Chehab Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, 94143, USA
Pages 405-420 | Received 04 Mar 1997, Accepted 30 Jun 1997, Published online: 07 Jul 2009

Citations (11)

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Read on this site (5)

Preetinanda M. Dash, Praveen K. Sahu, Siris Patel, Ranjeet S. Mashon, Kiran R. Kharat & Malay B. Mukherjee. (2018) Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia. Hemoglobin 42:4, pages 236-242.
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Monika R. Asnani, A. Williams & M. Reid. (2013) Splenic enlargement in adults with homozygous sickle cell disease: the Jamaican experience. Hematology 18:1, pages 46-49.
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SAMIR K. BALLAS & NARLA MOHANDAS. (2004) Sickle Red Cell Microrheology and Sickle Blood Rheology. Microcirculation 11:2, pages 209-225.
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Vip Viprakasit, Aranya Wiriyasateinkul, Benjamas Sattayasevana, Katie L. Miles & Vichai Laosombat. (2002) Hb G-MAKASSAR [β6(A3)Glu→Ala; CODON 6 (G G→G G)]: MOLECULAR CHARACTERIZATION, CLINICAL, AND HEMATOLOGICAL EFFECTS. Hemoglobin 26:3, pages 245-253.
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Samir K. Ballas. (2001) Effect of α-Globin Genotype on the Pathophysiology of Sickle Cell Disease. Pediatric Pathology & Molecular Medicine 20:2, pages 107-121.
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Articles from other publishers (6)

Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 185 260 .
Samir K. Ballas. (2018) Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management. Clinical Hemorheology and Microcirculation 68:2-3, pages 105-128.
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S. Abuamer, D. K. Shome, A. Jaradat, A. Radhi, J. P. Bapat, K. A. Sharif, J. Al‐Touq, A. Al‐Asheeri & A. Al‐Ajami. (2016) Frequencies and phenotypic consequences of association of α‐ and β‐thalassemia alleles with sickle‐cell disease in Bahrain. International Journal of Laboratory Hematology 39:1, pages 76-83.
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. 2006. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 139 189 .
Samir K. Ballas. (2002) Sickle Cell Anaemia. Drugs 62:8, pages 1143-1172.
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Samir K. Ballas. (1998) 7 Sickle cell disease: clinical management. Baillière's Clinical Haematology 11:1, pages 185-214.
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