Page last updated: 2024-11-06

hydroxyproline and Orphan Diseases

hydroxyproline has been researched along with Orphan Diseases in 1 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.

Orphan Diseases: Rare diseases that have not been well studied.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
EFRON, ML1
BIXBY, EM1
PRYLES, CV1

Other Studies

1 other study available for hydroxyproline and Orphan Diseases

ArticleYear
HYDROXYPROLINEMIA. II. A RARE METABOLIC DISEASE DUE TO A DEFICIENCY OF THE ENZYME "HYDROXYPROLINE OXIDASE".
    The New England journal of medicine, 1965, Jun-24, Volume: 272

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Blood; Blood Chemical

1965