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Num Mark Subjects (1-5 of 5) Year Entries
7 Found
1  

Peroxisomes -- See Also 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
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2 Peroxisomes.   3
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Peroxisomes Diseases -- See Peroxisomal disorders


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4 Peroxisomes -- Periodicals : PPAR research (Online)  2006- 1
5 Peroxisomes -- Receptors : Peroxisome proliferator-activated receptors : discovery and recent advances / Jihan A. Youssef, Mostafa Z. Badr  2013 1
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