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There are 18255 results for: content related to: Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin

  1. Hereditary Persistence of Fetal Haemoglobin

    The Thalassaemia Syndromes, Fourth Edition

    D.J. Weatherall, J.B. Clegg, Pages: 450–483, 2008

    Published Online : 16 APR 2008, DOI: 10.1002/9780470696705.ch10

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    Discovering the genetics underlying foetal haemoglobin production in adults

    British Journal of Haematology

    Volume 145, Issue 4, May 2009, Pages: 455–467, Swee Lay Thein and Stephan Menzel

    Article first published online : 5 MAR 2009, DOI: 10.1111/j.1365-2141.2009.07650.x

  3. The Molecular Pathology of the Thalassaemias

    The Thalassaemia Syndromes, Fourth Edition

    D.J. Weatherall, J.B. Clegg, Pages: 133–191, 2008

    Published Online : 16 APR 2008, DOI: 10.1002/9780470696705.ch4

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    Disorders of the synthesis of human fetal hemoglobin

    IUBMB Life

    Volume 60, Issue 2, February 2008, Pages: 94–111, Laura Manca and Bruno Masala

    Article first published online : 11 JAN 2008, DOI: 10.1002/iub.4

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    Advances in the understanding of haemoglobin switching

    British Journal of Haematology

    Volume 149, Issue 2, April 2010, Pages: 181–194, Vijay G. Sankaran, Jian Xu and Stuart H. Orkin

    Article first published online : 1 MAR 2010, DOI: 10.1111/j.1365-2141.2010.08105.x

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    UNDERSTANDING FETAL GLOBIN GENE EXPRESSION: A STEP TOWARDS EFFECTIVE HbF REACTIVATION IN HAEMOGLOBINOPATHIES

    British Journal of Haematology

    Volume 102, Issue 2, July 1998, Pages: 415–423, Stephen M. Jane and John M. Cunningham

    Article first published online : 25 DEC 2001, DOI: 10.1046/j.1365-2141.1998.00811.x

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    research paper: Role of the cold shock domain protein A in the transcriptional regulation of HBG expression

    British Journal of Haematology

    Volume 150, Issue 6, September 2010, Pages: 689–699, Raffaella Petruzzelli, Sara Gaudino, Giovanni Amendola, Raffaele Sessa, Stella Puzone, Rosanna Di Concilio, Giovanna D’Urzo, Maria Amendolara, Paola Izzo and Michela Grosso

    Article first published online : 2 SEP 2010, DOI: 10.1111/j.1365-2141.2010.08303.x

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    Factor binding to the human γ-globin gene distal CCAAT site: candidates for repression of the normal gene or activation of HPFH mutants

    British Journal of Haematology

    Volume 102, Issue 4, September 1998, Pages: 940–951, Partington and Patient

    Article first published online : 25 DEC 2001, DOI: 10.1046/j.1365-2141.1998.00849.x

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    The role of heterocellular hereditary persistence of fetal haemoglobin in β0-thalassaemia intermedia

    British Journal of Haematology

    Volume 114, Issue 4, September 2001, Pages: 899–906, Yen-Pei C. Chang, Roberto Littera, Raffaela Garau, Kirby D. Smith, George J. Dover, Sergio Iannelli, Enrico Cacace and Licinio Contu

    Article first published online : 20 DEC 2001, DOI: 10.1046/j.1365-2141.2001.03042.x

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    Detection of fetomaternal hemorrhage

    American Journal of Hematology

    Volume 87, Issue 4, April 2012, Pages: 417–423, Yeowon A. Kim and Robert S. Makar

    Article first published online : 9 JAN 2012, DOI: 10.1002/ajh.22255

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    Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2

    Annals of Human Genetics

    Volume 78, Issue 6, November 2014, Pages: 434–451, Stephan Menzel, Helen Rooks, Diana Zelenika, Siana N. Mtatiro, Akshala Gnanakulasekaran, Emma Drasar, Sharon Cox, Li Liu, Mariam Masood, Nicholas Silver, Chad Garner, Nisha Vasavda, Jo Howard, Julie Makani, Adekunle Adekile, Betty Pace, Tim Spector, Martin Farrall, Mark Lathrop and Swee Lay Thein

    Article first published online : 28 JUL 2014, DOI: 10.1111/ahg.12077

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    Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the β-globin gene cluster

    British Journal of Haematology

    Volume 148, Issue 1, January 2010, Pages: 154–160, Seung-Tae Lee, Eun-Hyung Yoo, Ji-Youn Kim, Jong-Won Kim and Chang-Seok Ki

    Article first published online : 5 OCT 2009, DOI: 10.1111/j.1365-2141.2009.07927.x

  13. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes

    British Journal of Haematology

    Volume 69, Issue 1, May 1988, Pages: 89–92, N. Murray, B. E. Serjeant and G. R. Serjeant

    Article first published online : 12 MAR 2008, DOI: 10.1111/j.1365-2141.1988.tb07607.x

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    Genetic modifiers of sickle cell disease

    American Journal of Hematology

    Volume 87, Issue 8, August 2012, Pages: 795–803, Martin H. Steinberg and Paola Sebastiani

    Article first published online : 28 MAY 2012, DOI: 10.1002/ajh.23232

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    Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin

    International Journal of Laboratory Hematology

    Volume 36, Issue 1, February 2014, Pages: 13–19, A. Amato, M. P. Cappabianca, M. Perri, I. Zaghis, P. Grisanti, D. Ponzini and P. Di Biagio

    Article first published online : 29 APR 2013, DOI: 10.1111/ijlh.12094

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    Fetal hemoglobin expression in the compound heterozygous state for −117 (G[RIGHTWARDS ARROW]A) Aγ HPFH and IVSII-745 (C[RIGHTWARDS ARROW]G) β+ thalassemia: A case study

    American Journal of Hematology

    Volume 61, Issue 2, June 1999, Pages: 139–143, George V.Z. Dedoussis, Klio Sinopoulou, Marilena Gyparaki and Aphroditi Loutradis

    Article first published online : 1 JUN 1999, DOI: 10.1002/(SICI)1096-8652(199906)61:2<139::AID-AJH12>3.0.CO;2-7

  17. Massive splenic infarction in an adolescent with hemoglobin S-HPFH

    Pediatric Blood & Cancer

    Volume 60, Issue 7, July 2013, Pages: E49–E51, Donna Whyte, Bernard Forget, David H.K. Chui, Hong-yuan Luo and Farzana Pashankar

    Article first published online : 31 DEC 2012, DOI: 10.1002/pbc.24444

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    Genetic strategies for the treatment of sickle cell anaemia

    British Journal of Haematology

    Volume 154, Issue 6, September 2011, Pages: 715–727, Jorge Mansilla-Soto, Isabelle Rivière and Michel Sadelain

    Article first published online : 28 JUN 2011, DOI: 10.1111/j.1365-2141.2011.08773.x

  19. Maximal γ-globin expression in the compound heterozygous state for –175 Gγ HPFH and β°39 nonsense thalassaemia: a case study

    European Journal of Haematology

    Volume 58, Issue 5, May 1997, Pages: 320–325, P. Pistidda, L. Frogheri, L. Guiso, L. Manca, F. Dore, L. Mura and M. Longinotti

    Article first published online : 24 APR 2009, DOI: 10.1111/j.1600-0609.1997.tb01678.x

  20. Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

    European Journal of Haematology

    Volume 92, Issue 6, June 2014, Pages: 514–520, Thiyagaraj Mayuranathan, Janakiram Rayabaram, Reena Das, Neeraj Arora, Eunice S. Edison, Mammen Chandy, Alok Srivastava and Shaji R. Velayudhan

    Article first published online : 15 MAR 2014, DOI: 10.1111/ejh.12276