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

Authors

2K

  1. SD
    Stephen D. Cederbaum

    University of California, Los Angeles, United States

    25 publications · 1.2K citations

    21

    h-index

  2. RB
    Ruth B. Caldwell

    Augusta University, United States

    21 publications · 1K citations

    16

    h-index

  3. ZX
    Zhimin Xu

    Augusta University, United States

    12 publications · 565 citations

    12

    h-index

  4. RW
    Robert W. Caldwell

    Augusta University, United States

    13 publications · 622 citations

    11

    h-index

  5. WW
    Wayne W. Grody

    University of California, Los Angeles, United States

    10 publications · 438 citations

    10

    h-index

1–5 of 2K

Venues

  1. PubMed

    Repository · 19 publications · 510 citations

    14

    h-index

  2. PLoS ONE

    13 publications · 473 citations

    12

    h-index

  3. The Journal of Immunology

    JI · 11 publications · 1.5K citations

    11

    h-index

  4. Molecular Genetics and Metabolism

    10 publications · 413 citations

    10

    h-index

  5. The Journal of Pediatrics

    9 publications · 225 citations

    9

    h-index

1–5