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
92
Douglas L. Rothman, I Magnusson, Gary W. Cline et al. · Proceedings of the National Academy of Sciences · 1995 · 326 citations
1–5 of 92
431
8
h-index
5
h-index
5
h-index
4
h-index
4
h-index
1–5 of 431
181
University of Urbino
Urbino, Italy
8 h-index
37 publications
894 citations
University Medical Center Utrecht
Utrecht, The Netherlands
5 h-index
18 publications
402 citations
Harvard University
Cambridge, United States
4 h-index
13 publications
1.4K citations
Utrecht University
Utrecht, The Netherlands
4 h-index
12 publications
336 citations
University of Pennsylvania
Philadelphia, United States
3 h-index
5 publications
520 citations

University of Amsterdam
Amsterdam, The Netherlands
3 h-index
5 publications
371 citations

City Of Hope National Medical Center
Duarte, United States
3 h-index
7 publications
262 citations
University of California, Los Angeles
Los Angeles, United States
3 h-index
13 publications
1.3K citations
1–8 of 181
11 publications · 327 citations
11
h-index
PNAS · 4 publications · 1.1K citations
4
h-index
JCI · 4 publications · 203 citations
4
h-index
BJH · 3 publications · 57 citations
3
h-index
JB · 3 publications · 90 citations
3
h-index
1–5