lysine has been researched along with Erythrophagocytic Lymphohistiocytosis, Familial 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ikeda, Y; Kosaki, K; Maruo, Y; Matsukawa, Y; Sakamoto, K; Taga, T | 1 |
| Dionisi-Vici, C; Ogier de Baulny, H; Schiff, M | 1 |
1 review(s) available for lysine and Erythrophagocytic Lymphohistiocytosis, Familial
| Article | Year |
|---|---|
Lysinuric protein intolerance (LPI): a multi organ disease by far more complex than a classic urea cycle disorder.
Topics: Arginine; Humans; Immune System; Kidney Diseases; Large Neutral Amino Acid-Transporter 1; Lung; Lymphohistiocytosis, Hemophagocytic; Lysine; Macrophage Activation Syndrome; Urea Cycle Disorders, Inborn | 2012 |
1 other study(ies) available for lysine and Erythrophagocytic Lymphohistiocytosis, Familial
| Article | Year |
|---|---|
Familial hemophagocytic lymphohistiocytosis syndrome due to lysinuric protein intolerance: a patient with a novel compound heterozygous pathogenic variant in SLC7A7.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport System y+L; Exons; Female; Humans; Lymphohistiocytosis, Hemophagocytic; Lysine; Mutation | 2022 |