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There are 47877 results for: content related to: Harnessing red cell membrane pathophysiology towards point-of-care diagnosis for sickle cell disease

  1. Sickle Cell Disease

    Standard Article

    Comprehensive Physiology

    Dhananjay K Kaul

    Published Online : 1 JAN 2011, DOI: 10.1002/cphy.cp020417

  2. You have full text access to this OnlineOpen article
    A non-electrolyte haemolysis assay for diagnosis and prognosis of sickle cell disease

    The Journal of Physiology

    Volume 591, Issue 6, March 2013, Pages: 1463–1474, C. Milligan, D. C. Rees, J. C. Ellory, A. Osei, J. A. Browning, A. Hannemann and J. S. Gibson

    Version of Record online : 4 FEB 2013, DOI: 10.1113/jphysiol.2012.246579

  3. Sickle Red Cell–Endothelium Interactions

    Microcirculation

    Volume 16, Issue 1, January 2009, Pages: 97–111, DHANANJAY K. KAUL, EILEEN FINNEGAN and GILDA A. BARABINO

    Version of Record online : 26 JAN 2010, DOI: 10.1080/10739680802279394

  4. The Endothelial Biology of Sickle Cell Disease: Inflammation and a Chronic Vasculopathy

    Microcirculation

    Volume 11, Issue 2, March 2004, Pages: 129–151, ROBERT P. HEBBEL, RAYMOND OSAROGIAGBON and DHANANJAY KAUL

    Version of Record online : 26 JAN 2010, DOI: 10.1080/10739680490278402

  5. In Vivo Studies of Sickle Red Blood Cells

    Microcirculation

    Volume 11, Issue 2, March 2004, Pages: 153–165, DHANANJAY K. KAUL and MARY E. FABRY

    Version of Record online : 26 JAN 2010, DOI: 10.1080/10739680490278457

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    Drugs for preventing red blood cell dehydration in people with sickle cell disease

    Intervention Review

    The Cochrane Library

    Srikanth Nagalla and Samir K Ballas

    Published Online : 4 MAR 2016, DOI: 10.1002/14651858.CD003426.pub5

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    The conductance of red blood cells from sickle cell patients: ion selectivity and inhibitors

    The Journal of Physiology

    Volume 590, Issue 9, May 2012, Pages: 2095–2105, Y.-L. Ma, D. C. Rees, J. S. Gibson and J. C. Ellory

    Version of Record online : 3 APR 2012, DOI: 10.1113/jphysiol.2012.229609

  8. The Not-So-Simple Process of Sickle Cell Vasoocclusion

    Microcirculation

    Volume 11, Issue 2, March 2004, Pages: 101–113, STEPHEN H. EMBURY

    Version of Record online : 26 JAN 2010, DOI: 10.1080/10739680490278277

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    2015 Clinical trials update in sickle cell anemia

    American Journal of Hematology

    Volume 90, Issue 10, October 2015, Pages: 934–950, Natasha Archer, Frédéric Galacteros and Carlo Brugnara

    Version of Record online : 21 SEP 2015, DOI: 10.1002/ajh.24116

  10. Sickle Red Cell Microrheology and Sickle Blood Rheology

    Microcirculation

    Volume 11, Issue 2, March 2004, Pages: 209–225, SAMIR K. BALLAS and NARLA MOHANDAS

    Version of Record online : 26 JAN 2010, DOI: 10.1080/10739680490279410

  11. Inhibition of Sickle Hemoglobin Polymerization as a Basis for Therapeutic Approaches to Sickle-Cell Anemia

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    Burger's Medicinal Chemistry and Drug Discovery

    Constance Tom Noguchi, Alan N. Schechter, John D. Haley and Donald J. Abraham

    Published Online : 15 JAN 2003, DOI: 10.1002/0471266949.bmc050

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    Prospective study of sickle cell trait and venous thromboembolism incidence

    Journal of Thrombosis and Haemostasis

    Volume 13, Issue 1, January 2015, Pages: 2–9, A. R. Folsom, W. Tang, N. S. Roetker, A. V. Kshirsagar, V. K. Derebail, P. L. Lutsey, R. Naik, J. S. Pankow, M. L. Grove, S. Basu, N. S. Key and M. Cushman

    Version of Record online : 11 DEC 2014, DOI: 10.1111/jth.12787

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    Differential oxygen sensitivity of the K+-Cl cotransporter in normal and sickle human red blood cells

    The Journal of Physiology

    Volume 511, Issue 1, August 1998, Pages: 225–234, J. S. Gibson, P. F. Speake and J. C. Ellory

    Version of Record online : 22 SEP 2004, DOI: 10.1111/j.1469-7793.1998.225bi.x

  14. Hydroxyurea (hydroxycarbamide) for sickle cell disease

    Intervention Review

    The Cochrane Library

    Sarah J Nevitt, Ashley P Jones and Jo Howard

    Published Online : 20 APR 2017, DOI: 10.1002/14651858.CD002202.pub2

  15. Normal saline is associated with increased sickle red cell stiffness and prolonged transit times in a microfluidic model of the capillary system

    Microcirculation

    Volume 24, Issue 5, July 2017, Marcus A. Carden, Meredith Fay, Yumiko Sakurai, Brynn McFarland, Sydney Blanche, Caleb DiPrete, Clinton H. Joiner, Todd Sulchek and Wilbur A. Lam

    Version of Record online : 10 JUL 2017, DOI: 10.1111/micc.12353

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    Reconstructing sickle cell disease: A data-based analysis of the “hyperhemolysis paradigm” for pulmonary hypertension from the perspective of evidence-based medicine

    American Journal of Hematology

    Volume 86, Issue 2, February 2011, Pages: 123–154, Robert P. Hebbel

    Version of Record online : 21 JAN 2011, DOI: 10.1002/ajh.21952

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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

    Version of Record online : 28 MAY 2012, DOI: 10.1002/ajh.23232

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    Predicting clinical severity in sickle cell anaemia

    British Journal of Haematology

    Volume 129, Issue 4, May 2005, Pages: 465–481, M. H. Steinberg

    Version of Record online : 1 MAR 2005, DOI: 10.1111/j.1365-2141.2005.05411.x

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    Sickle red blood cells accumulate in tumor

    Magnetic Resonance in Medicine

    Volume 50, Issue 6, December 2003, Pages: 1209–1214, S.L. Brown, J.R. Ewing, T.N. Nagaraja, P.S. Swerdlow, Y. Cao, J.D. Fenstermacher and J.H. Kim

    Version of Record online : 21 NOV 2003, DOI: 10.1002/mrm.10646

  20. Magnesium for treating sickle cell disease

    Intervention Review

    The Cochrane Library

    Nan Nitra Than, Htoo Htoo Kyaw Soe, Senthil K Palaniappan, Adinegara BL Abas and Lucia De Franceschi

    Published Online : 14 APR 2017, DOI: 10.1002/14651858.CD011358.pub2