Page last updated: 2024-10-25

clofibrate and Peroxisomal Disorders

clofibrate has been researched along with Peroxisomal Disorders in 1 studies

angiokapsul: contains clofibrate & insoitolnicotinate

Peroxisomal Disorders: A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders.

Research

Studies (1)

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

Authors

AuthorsStudies
Sepúlveda, J1
Gutiérrez, F1
Moreno, M1
Hernández, A1

Other Studies

1 other study available for clofibrate and Peroxisomal Disorders

ArticleYear
Peroxisomal proliferation induced by treatment with clofibrate in a patient with a peroxisomal disease.
    Cell biochemistry and biophysics, 2000, Volume: 32 Spring

    Topics: Adolescent; Adult; Animals; Clofibrate; Humans; Hypolipidemic Agents; Male; Mice; Peroxisomal Disord

2000