hydroxyproline has been researched along with Caffey Disease in 4 studies
Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (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 |
---|---|
Woodhouse, NJ | 1 |
Fisher, MT | 1 |
Sigurdsson, G | 1 |
Joplin, GF | 1 |
MacIntyre, I | 1 |
Salzer, M | 1 |
Schwägerl, W | 1 |
Alderman, MH | 1 |
Frimpter, GW | 1 |
Isaacs, M | 1 |
Scheiner, E | 1 |
Thompson, RC | 1 |
Gaull, GE | 1 |
Horwitz, SJ | 1 |
Schenk, RK | 1 |
4 other studies available for hydroxyproline and Caffey Disease
Article | Year |
---|---|
Paget's disease in a 5-year-old: acute response to human calcitonin.
Topics: Acid Phosphatase; Alkaline Phosphatase; Bone and Bones; Calcitonin; Calcium; Child, Preschool; Femor | 1972 |
[Hyperostosis corticalis infantilis. (Roske-Caffey syndrome].
Topics: Age Factors; Alkaline Phosphatase; Blood Sedimentation; Bone and Bones; Diagnosis, Differential; Hum | 1967 |
Glycylproline peptiduria in familial hyperostosis of obscure nature.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Ion Exchange; Chromatograph | 1969 |
Hereditary hyperphosphatasia. Studies of three siblings.
Topics: Acid Phosphatase; Adolescent; Adult; Alkaline Phosphatase; Amino Acids; Bone and Bones; Calcium; Chi | 1969 |