Showing 1 - 3 results of 3 for search '"non‐spherocytic hemolytic anemia"', query time: 0.85s Refine Results
  1. 1
    Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

    Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family by Sasha Waldstein, Sarah Arnold‐Croop, Laura Carrel, M. Elaine Eyster

    Published 2021-08-01
    Subjects:
    Get full text
    Article
  2. 2
    Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review

    Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review by Linlin Xu, Dina Zhu, Yanxia Zhang, Guanxia Liang, Min Liang, Xiaofeng Wei, Xiaoqing Feng, Xuedong Wu, Xuan Shang

    Published 2021-06-01
    Subjects:
    Get full text
    Article
  3. 3
    A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report

    A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report by Karolina Maciak, Anna Adamowicz-Salach, Jaroslaw Poznanski, Monika Gora, Jan Fronk, Beata Burzynska

    Published 2020-10-01
    Subjects: “…congenital non-spherocytic hemolytic anemia…”
    Get full text
    Article

Search Tools: