Arginase Deficiency
Arginase Deficiency is a rare autosomal recessive urea cycle disorder characterized by a deficiency of the enzyme arginase 1, leading to the impaired hydrolysis of arginine into ornithine and urea, resulting in hyperargininemia and progressive neurological deterioration.
382
Publications
20.1K
Citations
2K
Authors
620
Institutions
Publications per year
2017–2026
94
382
Matthias Hesse, Manuel Modolell, Anne Camille La Flamme et al. · The Journal of Immunology · 2001 · 681 citations · Full text
Suppression of T-cell functions by human granulocyte arginase
Markus Munder · Blood · 2006 · 415 citations · Full text
Alain P. Gobert, David J. McGee, Mahmood Akhtar et al. · Proceedings of the National Academy of Sciences · 2001 · 374 citations · Full text
Claudia R. Morris, Sidney M. Morris, Ward Hagar et al. · American Journal of Respiratory and Critical Care Medicine · 2003 · 327 citations
1–5 of 382
2K
University of California, Los Angeles, United States
25 publications · 1.2K citations
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12
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11
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10
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1–5 of 2K
620
University of California, Los Angeles
Los Angeles, United States
23 h-index
145 publications
6.6K citations
Baylor College of Medicine
Houston, United States
16 h-index
50 publications
2.1K citations

Augusta University
Augusta, United States
16 h-index
142 publications
5.8K citations
Charlie Norwood VA Medical Center
Augusta, United States
12 h-index
57 publications
2.5K citations
Augusta University Health
Augusta, United States
10 h-index
70 publications
3.9K citations
University of Pittsburgh
Pittsburgh, United States
10 h-index
21 publications
3.6K citations
Harvard University
Cambridge, United States
9 h-index
34 publications
2.1K citations
Discovery Institute
Seattle, United States
9 h-index
63 publications
2.8K citations
1–8 of 620
Repository · 19 publications · 510 citations
14
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13 publications · 473 citations
12
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JI · 11 publications · 1.5K citations
11
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10 publications · 413 citations
10
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9 publications · 225 citations
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