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Peroxisomal disorders.
Moser HW, Bergin A, Cornblath D. Moser HW, et al. Biochem Cell Biol. 1991 Jul;69(7):463-74. doi: 10.1139/o91-070. Biochem Cell Biol. 1991. PMID: 1724376 Review.
The recognition that the organelle is significant in mammals was ushered in by Paul Lazarow's observation that rat peroxisomes catalyze the beta-oxidation of fatty acids. ...Respect for the physiological role of the peroxisome in man has been heightened by our recent recog …
The recognition that the organelle is significant in mammals was ushered in by Paul Lazarow's observation that rat peroxisomes cataly …
Child neurology: Zellweger syndrome.
Lee PR, Raymond GV. Lee PR, et al. Neurology. 2013 May 14;80(20):e207-10. doi: 10.1212/WNL.0b013e3182929f8e. Neurology. 2013. PMID: 23671347 Free PMC article. Review.
Zellweger syndrome (ZS) is a severe manifestation of disease within the spectrum of peroxisome biogenesis disorders that includes neonatal adrenoleukodystrophy, infantile Refsum disease, and rhizomelic chondroplasia punctata. ...
Zellweger syndrome (ZS) is a severe manifestation of disease within the spectrum of peroxisome biogenesis disorders that includes neo …
Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I. Aubourg P, et al. Pediatr Res. 1993 Sep;34(3):270-6. doi: 10.1203/00006450-199309000-00006. Pediatr Res. 1993. PMID: 7510868
Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum's disease are genetic disorders characterized by the virtual absence of catalase-positive peroxisomes and a general impairment of peroxisomal functions. ...
Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum's disease are genetic disorders characterized by the virtual …