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penicillamine and Hyperbilirubinemia, Hereditary

penicillamine has been researched along with Hyperbilirubinemia, Hereditary in 1 studies

Penicillamine: 3-Mercapto-D-valine. The most characteristic degradation product of the penicillin antibiotics. It is used as an antirheumatic and as a chelating agent in Wilson's disease.
penicillamine : An alpha-amino acid having the structure of valine substituted at the beta position with a sulfanyl group.

Hyperbilirubinemia, Hereditary: Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.

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
Smallwood, RA1
Williams, HA1
Rosenoer, VM1
Sherlock, S1

Other Studies

1 other study available for penicillamine and Hyperbilirubinemia, Hereditary

ArticleYear
Liver-copper levels in liver disease: studies using neutron activation analysis.
    Lancet (London, England), 1968, Dec-21, Volume: 2, Issue:7582

    Topics: Activation Analysis; Biliary Tract Diseases; Biopsy; Chemical and Drug Induced Liver Injury; Cholest

1968