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hydroxyproline and Anemia, Sickle Cell

hydroxyproline has been researched along with Anemia, Sickle Cell 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.

Anemia, Sickle Cell: A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.

Research Excerpts

ExcerptRelevanceReference
"Hydroxyproline excretion was significantly higher in the sickle cell patients than in controls."1.28Urinary hydroxyproline and serum alkaline phosphatase in sickle cell disease. ( Addae, SK; Adzaku, FK; Annobil, SH; Kadoummi, OF; Mohammed, SM; Richards, JT; Suleiman, SA, 1991)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mohammed, SM1
Suleiman, SA1
Addae, SK1
Annobil, SH1
Adzaku, FK1
Kadoummi, OF1
Richards, JT1

Other Studies

1 other study available for hydroxyproline and Anemia, Sickle Cell

ArticleYear
Urinary hydroxyproline and serum alkaline phosphatase in sickle cell disease.
    Clinica chimica acta; international journal of clinical chemistry, 1991, Dec-16, Volume: 203, Issue:2-3

    Topics: Adolescent; Adult; Aging; Alkaline Phosphatase; Anemia, Sickle Cell; Female; Humans; Hydroxyproline;

1991