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Hematology Volume 12, 2007 - Issue 2
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Myeloproliferative Disease

Genetically heterogeneous origins of idiopathic erythrocytosis

Me Lanie J PercyDepartment of HaematologyBelfast City Hospital, Floor C, Lisburn Road, Belfast BT9 7AB, Northern Ireland, UK
Pages 131-139 | Published online: 04 Sep 2013

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Mary Frances McMullin. (2010) HIF pathway mutations and erythrocytosis. Expert Review of Hematology 3:1, pages 93-101.
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H. Chang & L.-Y. Shih. (2009) CONCURRENCE OF MULTIPLE MYELOMA AND IDIOPATHIC ERYTHROCYTOSIS. Acta Clinica Belgica 64:5, pages 434-435.
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Articles from other publishers (18)

Lucie Sochorcova, Katarina Hlusickova Kapralova, Jana Fialova Kucerova, Dagmar Pospisilova, Daniela Prochazkova, Ondrej Jahoda, Simona Kurekova, Barbora Kralova, Martina Divoka, Jana Navratilova, Jirina Manakova, Eva Kriegova, Karel Indrak, Edgar Faber, Vladimir Divoky & Monika Horvathova. (2023) Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen‐sensing pathway from primary familial and congenital polycythaemia. British Journal of Haematology 202:3, pages 674-685.
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Kai Wille, Parvis Sadjadian & Martin Griesshammer. (2022) Differenzialdiagnose der Erythrozytose – Ursachen und klinische Bedeutung. Transfusionsmedizin 12:02, pages 88-94.
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Kai Wille, Parvis Sadjadian & Martin Griesshammer. (2019) Differenzialdiagnose der Erythrozytose – Ursachen und klinische Bedeutung. DMW - Deutsche Medizinische Wochenschrift 144:02, pages 128-135.
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Ping-hung Chen, Huiyu Yao & Lily Jun-shen Huang. (2017) Cytokine Receptor Endocytosis: New Kinase Activity-Dependent and -Independent Roles of PI3K. Frontiers in Endocrinology 8.
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Graham W. Magor, Michael R. Tallack, Nathan M. Klose, Debra Taylor, Darren Korbie, Peter Mollee, Matt Trau & Andrew C. Perkins. (2016) Rapid Molecular Profiling of Myeloproliferative Neoplasms Using Targeted Exon Resequencing of 86 Genes Involved in JAK-STAT Signaling and Epigenetic Regulation. The Journal of Molecular Diagnostics 18:5, pages 707-718.
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M. F. McMullin. (2016) Congenital erythrocytosis. International Journal of Laboratory Hematology 38, pages 59-65.
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Wojciech Gorczyca. 2014. Atlas of Differential Diagnosis in Neoplastic Hematopathology, Third Edition. Atlas of Differential Diagnosis in Neoplastic Hematopathology, Third Edition 503 516 .
Carla Luana Dinardo, Paulo Caleb Junior Lima Santos, Isolmar Tadeu Schettert, Renata Alonso Gadi Soares, Jose Eduardo Krieger & Alexandre Costa Pereira. (2013) Investigation of Genetic Disturbances in Oxygen Sensing and Erythropoietin Signaling Pathways in Cases of Idiopathic Erythrocytosis. Genetics Research International 2013, pages 1-4.
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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 Frances McMullin, Chao Wu, Melanie J Percy & Wei Tong. (2011) A nonsynonymous LNK polymorphism associated with idiopathic erythrocytosis . American Journal of Hematology 86:11, pages 962-964.
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Asterios S. Tsiftsoglou, Ioannis S. Vizirianakis & John Strouboulis. (2009) Erythropoiesis: Model systems, molecular regulators, and developmental programs. IUBMB Life 61:8, pages 800-830.
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Rita Sulahian, Ondine Cleaver & Lily Jun-shen Huang. (2009) Ligand-induced EpoR internalization is mediated by JAK2 and p85 and is impaired by mutations responsible for primary familial and congenital polycythemia. Blood 113:21, pages 5287-5297.
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M M Patnaik & A Tefferi. (2009) The complete evaluation of erythrocytosis: congenital and acquired. Leukemia 23:5, pages 834-844.
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Mary Frances McMullin. (2009) Idiopathic erythrocytosis: a disappearing entity. Hematology 2009:1, pages 629-635.
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Melanie J. Percy & Elisa Rumi. (2008) Genetic origins and clinical phenotype of familial and acquired erythrocytosis and thrombocytosis. American Journal of Hematology 84:1, pages 46-54.
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M. F. McMULLIN. (2008) The classification and diagnosis of erythrocytosis. International Journal of Laboratory Hematology.
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Thomas G. Smith, Peter A. Robbins & Peter J. Ratcliffe. (2008) The human side of hypoxia-inducible factor. British Journal of Haematology 141:3, pages 325-334.
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Melanie J. Percy, Mayka Sanchez, Sabina Swierczek, Mary Frances McMullin, Mariluz P. Mojica-Henshaw, Martina U. Muckenthaler, Josef T. Prchal & Matthias W. Hentze. (2007) Is congenital secondary erythrocytosis/polycythemia caused by activating mutations within the HIF-2α iron-responsive element?. Blood 110:7, pages 2776-2777.
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