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Academic Journal

Clearance of pathogenic erythrocytes is maintained despite spleen dysfunction in children with sickle cell disease.

  • Authors : Sissoko A; Université Paris Cité, Inserm, BIGR, Paris, France.; Cissé A

Subjects: Anemia, Sickle Cell*/Anemia, Sickle Cell*/Anemia, Sickle Cell*/blood ; Anemia, Sickle Cell*/Anemia, Sickle Cell*/Anemia, Sickle Cell*/complications ; Spleen*/Spleen*/Spleen*/pathology

  • Source: American journal of hematology [Am J Hematol] 2024 Dec; Vol. 99 (12), pp. 2267-2278. Date of Electronic Publication: 2024 Sep 17.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Swaying sickle cell research forward in support of patient reported outcomes.

Subjects: Anemia, Sickle Cell* ; Erythrocytes, Abnormal*; Humans

  • Source: American journal of hematology [Am J Hematol] 2021 Apr 01; Vol. 96 (4), pp. 402-403. Date of Electronic Publication: 2021 Jan 22.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Schistocytosis is not always microangiopathic hemolytic anemia.

  • Authors : Lofaro T; Department of Haematology, Hammersmith Hospital, London, UK.; Bain BJ

Subjects: Anemia, Hemolytic*/Anemia, Hemolytic*/Anemia, Hemolytic*/blood ; Anemia, Hemolytic*/Anemia, Hemolytic*/Anemia, Hemolytic*/pathology ; Erythrocytes, Abnormal*/Erythrocytes, Abnormal*/Erythrocytes, Abnormal*/metabolism

  • Source: American journal of hematology [Am J Hematol] 2020 Nov; Vol. 95 (11), pp. 1421-1422. Date of Electronic Publication: 2020 Jun 09.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

MYH9-related disease mutations cause abnormal red blood cell morphology through increased myosin-actin binding at the membrane.

  • Authors : Smith AS; Department of Molecular Medicine, The Scripps Research Institute, La Jolla, California.; Pal K

Subjects: Actins*/Actins*/Actins*/genetics ; Actins*/Actins*/Actins*/metabolism ; Erythrocyte Membrane*/Erythrocyte Membrane*/Erythrocyte Membrane*/genetics MYH9-Related Disorders

  • Source: American journal of hematology [Am J Hematol] 2019 Jun; Vol. 94 (6), pp. 667-677. Date of Electronic Publication: 2019 Apr 17.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Editorial & Opinion

Erythrocyte ATP, a possible therapeutic approach for sickle cell disease.

  • Authors : Hoffman JF; Department of Cellular and Molecular Physiology, Yale University, School of Medical, New Haven, Connecticut.

Subjects: Adenosine Triphosphate/Adenosine Triphosphate/Adenosine Triphosphate/*metabolism ; Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*metabolism ; Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*therapy

  • Source: American journal of hematology [Am J Hematol] 2019 May; Vol. 94 (5), pp. E117. Date of Electronic Publication: 2019 Feb 14.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients.

  • Authors : Rab MAE; Laboratory of Clinical Chemistry & Hematology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.; Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Subjects: Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*blood ; Benzaldehydes/Benzaldehydes/Benzaldehydes/*pharmacology ; Erythrocytes, Abnormal/Erythrocytes, Abnormal/Erythrocytes, Abnormal/*metabolism

  • Source: American journal of hematology [Am J Hematol] 2019 May; Vol. 94 (5), pp. 575-584. Date of Electronic Publication: 2019 Mar 08.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Sickle cells produce functional immune modulators and cytotoxics.

  • Authors : Sun CW; Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, School of Medicine, Birmingham, Alabama.; Wu LC

Subjects: Anemia, Sickle Cell*/Anemia, Sickle Cell*/Anemia, Sickle Cell*/blood ; Cytotoxicity, Immunologic*/Cytotoxicity, Immunologic*/Cytotoxicity, Immunologic*/genetics; Erythrocytes, Abnormal/Erythrocytes, Abnormal/Erythrocytes, Abnormal/*immunology

  • Source: American journal of hematology [Am J Hematol] 2017 Oct; Vol. 92 (10), pp. 981-988. Date of Electronic Publication: 2017 Aug 17.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Report

Effects of hydroxyurea on F-cells in sickle cell disease and potential impact of a second fetal globin inducer.

  • Authors : Dai Y; Cancer Center, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.; Cancer Center, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts.

Subjects: Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*blood ; Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*drug therapy ; Erythrocytes, Abnormal/Erythrocytes, Abnormal/Erythrocytes, Abnormal/*metabolism

  • Source: American journal of hematology [Am J Hematol] 2017 Jan; Vol. 92 (1), pp. E10-E11. Date of Electronic Publication: 2016 Nov 18.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The delay time in sickle cell disease after 40 years: A paradigm assessed.

  • Authors : Ferrone FA; Department of Physics, Drexel University, Philadelphia, Pennsylvania.

Subjects: Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*blood ; Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*diagnosis ; Erythrocytes, Abnormal/Erythrocytes, Abnormal/Erythrocytes, Abnormal/*metabolism

  • Source: American journal of hematology [Am J Hematol] 2015 May; Vol. 90 (5), pp. 438-45. Date of Electronic Publication: 2015 Feb 25.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.

  • Authors : Kucukal E; Department of Mechanical and Aerospace Engineering, Case Western Reserve University, Cleveland, Ohio.; Man Y

Subjects: Blood Viscosity* ; Cell Adhesion*; Anemia, Sickle Cell/Anemia, Sickle Cell/Anemia, Sickle Cell/*blood

  • Source: American journal of hematology [Am J Hematol] 2020 Nov; Vol. 95 (11), pp. 1246-1256. Date of Electronic Publication: 2020 Aug 10.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 7610369 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  100 results for ""Erythrocytes, Abnormal""