arginine has been researched along with Lysosomal Enzyme Disorders in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Du, H; Gartner, A; Liu, B; Rutkowski, R; Wang, X | 1 |
Ohashi, T; Ohno, K | 1 |
1 review(s) available for arginine and Lysosomal Enzyme Disorders
Article | Year |
---|---|
[Diagnosis and treatment of hereditary neurological disorders during childhood].
Topics: alpha-Galactosidase; Arginine; Child; Coenzymes; Glucosylceramidase; Heredodegenerative Disorders, Nervous System; Humans; Isoenzymes; Lysosomal Storage Diseases; Mitochondrial Diseases; Molecular Diagnostic Techniques; Myotonic Dystrophy; Peripheral Nervous System Diseases; Peroxisomal Disorders; Trinucleotide Repeats; Ubiquinone; Vitamin E | 2007 |
1 other study(ies) available for arginine and Lysosomal Enzyme Disorders
Article | Year |
---|---|
LAAT-1 is the lysosomal lysine/arginine transporter that maintains amino acid homeostasis.
Topics: Amino Acid Transport Systems; Amino Acid Transport Systems, Basic; Animals; Arginine; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Chlorocebus aethiops; COS Cells; Cysteamine; Homeostasis; Humans; Lysine; Lysosomal Storage Diseases; Lysosomes | 2012 |