Hexokinase Deficiency

Hexokinase Deficiency is a rare inherited metabolic disorder characterized by a deficiency in the hexokinase enzyme, which impairs the first step of glycolysis and leads to abnormal glucose metabolism in red blood cells and other tissues.

92

Publications

6.4K

Citations

431

Authors

181

Institutions

Publications per year

2017–2026

11

Authors

431

  1. MM
    Mauro Magnani

    University of Urbino, Italy

    8 publications · 202 citations

    8

    h-index

  2. GF
    G Fornaini

    University of Urbino, Italy

    5 publications · 113 citations

    5

    h-index

  3. GR
    Gert Rijksen

    Utrecht University, Netherlands

    5 publications · 149 citations

    5

    h-index

  4. GE
    G. E. J. Staal

    Utrecht University, Netherlands

    4 publications · 104 citations

    4

    h-index

  5. EB
    Ernest Beutler

    City Of Hope National Medical Center, United States

    4 publications · 147 citations

    4

    h-index

1–5 of 431

Venues

  1. Blood

    11 publications · 327 citations

    11

    h-index

  2. Proceedings of the National Academy of Sciences

    PNAS · 4 publications · 1.1K citations

    4

    h-index

  3. Journal of Clinical Investigation

    JCI · 4 publications · 203 citations

    4

    h-index

  4. British Journal of Haematology

    BJH · 3 publications · 57 citations

    3

    h-index

  5. Journal of Bacteriology

    JB · 3 publications · 90 citations

    3

    h-index

1–5