galactosylhydroxylysine has been researched along with Alport Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ananenko, AA; Daĭkhin, EI; Ignatova, MS; Klembovskiĭ, AI; Vel'tishchev, IuE | 1 |
| Monnens, LA; Schröder, CH; Trijbels, JM; van Lith-Zanders, HM; Veerkamp, JH | 1 |
| Langeveld, JP; Monnens, LA; Schröder, CH; Trijbels, JM; van Lith-Zanders, HM; Veerkamp, JH | 1 |
3 other study(ies) available for galactosylhydroxylysine and Alport Syndrome
| Article | Year |
|---|---|
[Renal excretion of connective tissue metabolites and the state of the glomerular basement membranes in hereditary nephritis in children].
Topics: Adolescent; Basement Membrane; Child; Child, Preschool; Connective Tissue; Female; Glycosaminoglycans; Humans; Hydroxylysine; Hydroxyproline; Infant; Kidney Glomerulus; Male; Nephritis, Hereditary | 1981 |
The urinary excretion of total hydroxylysine and its glycosides in normal persons, and in patients suffering from Alport's syndrome--contribution of the peptide-bound fraction.
Topics: Adolescent; Adult; Age Factors; Child; Humans; Hydroxylysine; Nephritis, Hereditary; Protein Binding; Sex Factors | 1987 |
Urinary excretion of hydroxylysine and its glycosides in Alport's syndrome and several other glomerulopathies.
Topics: Adolescent; Adult; Child; Child, Preschool; Female; Glomerulonephritis; Glomerulonephritis, IGA; Hematuria; Humans; Hydroxylysine; Kidney Diseases; Male; Nephritis, Hereditary; Nephrotic Syndrome | 1986 |