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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 3
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THROMBOTIC EVENTS IN COMPOUND HETEROZYGOTES FOR A HIGH AFFINITY HEMOGLOBIN VARIANT: Hb MILLEDGEVILLE [α44(CE2)Pro→Leu (α2)] AND FACTOR V LEIDEN

Michel Hanss Edouard Herriot Hospital, Hemostasis Laboratory, Lyon Cedex 03, 69437, France
,
Philippe Lacan Molecular Pathology Unit, Department of Biochemistry, Edouard Herriot Hospital, 5, Place d'Arsonval, Lyon Cedex 03, 69437, France
,
Martine Aubry Molecular Pathology Unit, Department of Biochemistry, Edouard Herriot Hospital, 5, Place d'Arsonval, Lyon Cedex 03, 69437, France
,
Anne Lienhard Edouard Herriot Hospital, Hemostasis Laboratory, Lyon Cedex 03, 69437, France
&
Alain Francina Molecular Pathology Unit, Department of Biochemistry, Edouard Herriot Hospital, 5, Place d'Arsonval, Lyon Cedex 03, 69437, France
Pages 285-290 | Received 04 Apr 2002, Accepted 15 May 2002, Published online: 07 Jul 2009

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Sona B. Nair, Arundhati S. Athalye, Madhavi Panphalia & Firuza R. Parikh. (2022) First Report of an α Chain Variant [Hb Coombe Park (HBA2: c.382A>G)] from India, Coinherited with a Novel SERPINC1 Gene Mutation: A Double Whammy?. Hemoglobin 46:5, pages 269-271.
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Amelia Oliveira, Dana Warcel, Nancy Huntley, Perla Eleftheriou & John B. Porter. (2016) Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and α-Thalassemia: A Clinical Update. Hemoglobin 40:2, pages 127-129.
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Susumu Inoue, Jennifer L. Oliveira, James D. Hoyer & Mahesh Sharman. (2012) Symptomatic Erythrocytosis Associated with a Compound Heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu, GTG>TTG]. Hemoglobin 36:4, pages 362-370.
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Dima El-Sharkawi, Chris Fisher, Sachin Khambadkone, Adrian D. Stephens & John B. Porter. (2012) Secondary Erythrocytosis Due to Compound Homozygosity, but not Compound Heterozygosity, for Hb Luton and α-Thalassemia: A Family Study. Hemoglobin 36:1, pages 7-17.
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Articles from other publishers (6)

Naseema Gangat, Jennifer L. Oliveira, James D. Hoyer, Mrinal M. Patnaik, Animesh Pardanani & Ayalew Tefferi. (2021) High‐oxygen‐affinity hemoglobinopathy‐associated erythrocytosis: Clinical outcomes and impact of therapy in 41 cases. American Journal of Hematology 96:12, pages 1647-1654.
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Jovana Yudin & Madeleine Verhovsek. (2019) How we diagnose and manage altered oxygen affinity hemoglobin variants. American Journal of Hematology 94:5, pages 597-603.
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O. Mangin. (2017) High oxygen affinity hemoglobins. La Revue de Médecine Interne 38:2, pages 106-112.
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Shinobu Tamura, Tadahiko Tamura, Hiroya Gima, Akinori Nishikawa, Yukiharu Okamoto, Nobuo Kanazawa, Luis Relvas, Elizabete Cunha, Mary Frances McMullin & Celeste Bento. (2015) A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda. Internal Medicine 54:18, pages 2389-2393.
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Mary Frances McMullin. (2012) Diagnosis and management of congenital and idiopathic erythrocytosis. Therapeutic Advances in Hematology 3:6, pages 391-398.
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Mary F. McMullin, D. Bareford, P. Campbell, A. R. Green, Claire Harrison, Beverley Hunt, D. Oscier, M. I. Polkey, J. T. Reilly, E. Rosenthal, Kate Ryan, T. C. Pearson & Bridget Wilkins. (2005) Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis. British Journal of Haematology 130:2, pages 174-195.
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