Page last updated: 2024-11-07

penicillamine and Genetic Diseases

penicillamine has been researched along with Genetic Diseases in 3 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.

Research Excerpts

ExcerptRelevanceReference
" (1) The chronic administration of isoniazid for the prevention or treatment of tuberculosis can produce peripheral neuropathy which can be prevented by the concurrent administration of pyridoxine."2.36Drug-pyridoxal phosphate interactions. ( Al-Sayegh, A; Ebadi, M; Gessert, CF, 1982)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Momoki, T1
Terauchi, Y1
Ebadi, M1
Gessert, CF1
Al-Sayegh, A1
Shmidt, EV1
Tkachev, RA1
Markova, ED1

Reviews

2 reviews available for penicillamine and Genetic Diseases

ArticleYear
[Aceruloplasminemia (hereditary ceruloplasmin deficiency) and diabetes mellitus].
    Nihon rinsho. Japanese journal of clinical medicine, 2006, Sep-28, Volume: Suppl 3

    Topics: Brain Diseases; Ceruloplasmin; Diabetes Mellitus; Diagnosis, Differential; Genetic Diseases, Inborn;

2006
Drug-pyridoxal phosphate interactions.
    Quarterly reviews on drug metabolism and drug interactions, 1982, Volume: 4, Issue:4

    Topics: Animals; Contraceptives, Oral, Hormonal; Depressive Disorder; Disease; Drug Interactions; Drug Thera

1982

Other Studies

1 other study available for penicillamine and Genetic Diseases

ArticleYear
[Key problems of clinical neurogenetics].
    Vestnik Akademii meditsinskikh nauk SSSR, 1976, Issue:7

    Topics: Diagnosis, Differential; Drug Evaluation; Genetic Diseases, Inborn; Humans; Levodopa; Nervous System

1976