Literature DB >> 2675566

Peroxisomal diseases.

H W Moser1.   

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Year:  1989        PMID： 2675566

Source DB:  PubMed          Journal:  Adv Pediatr        ISSN： 0065-3101


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  5 in total

1.  Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids.

Authors:  H Mandel; M Berant; A Aizin; R Gershony; S Hemmli; R B Schutgens; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient.

Authors:  R Santer; A Claviez; H D Oldigs; J Schaub; R B Schutgens; R J Wanders
Journal:  Eur J Pediatr       Date:  1993-04       Impact factor: 3.183

Review 3.  The inherited leukodystrophies: a clinical overview.

Authors:  J Aicardi
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

4.  The deficient degradation of synthetic 2- and 3-methyl-branched fatty acids in fibroblasts from patients with peroxisomal disorders.

Authors:  P P Van Veldhoven; S Huang; H J Eyssen; G P Mannaerts
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

5.  Plasma lipoproteins and monocyte-macrophages in a peroxisome-deficient system: study of a patient with infantile refsum disease.

Authors:  H Mandel; M Berant; D Meiron; A Aizin; J Oiknine; J G Brook; M Aviram
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
  5 in total

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