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4. [Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers]. Molzer B; Stöckler S; Bernheimer H Wien Klin Wochenschr; 1992; 104(21):665-70. PubMed ID: 1282286 [TBL] [Abstract][Full Text] [Related]
5. [Zellweger syndrome, neonatal adrenoleukodystrophy or infantile Refsum's disease in a case with generalized peroxisome defect?]. Schmitt K; Molzer B; Stöckler S; Tulzer G; Tulzer W Wien Klin Wochenschr; 1993; 105(11):320-2. PubMed ID: 7687405 [TBL] [Abstract][Full Text] [Related]
6. Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders. Hughes JL; Poulos A; Robertson E; Chow CW; Sheffield LJ; Christodoulou J; Carter RF Virchows Arch A Pathol Anat Histopathol; 1990; 416(3):255-64. PubMed ID: 1689088 [TBL] [Abstract][Full Text] [Related]
7. The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma. Aubourg P; Robain O; Rocchiccioli F; Dancea S; Scotto J J Neurol Sci; 1985; 69(1-2):9-25. PubMed ID: 4009207 [TBL] [Abstract][Full Text] [Related]
8. Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes. Poulos A; Sharp P; Johnson D Neurology; 1989 Jan; 39(1):44-7. PubMed ID: 2462697 [TBL] [Abstract][Full Text] [Related]
9. Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy. Small GM; Santos MJ; Imanaka T; Poulos A; Danks DM; Moser HW; Lazarow PB J Inherit Metab Dis; 1988; 11(4):358-71. PubMed ID: 2468817 [TBL] [Abstract][Full Text] [Related]
10. 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 Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868 [TBL] [Abstract][Full Text] [Related]
11. Infantile Refsum's disease: a peroxisomal storage disorder? Manson JI; Pollard AC; Poulos A; Carter RF Clin Exp Neurol; 1985; 21():283-7. PubMed ID: 2436838 [TBL] [Abstract][Full Text] [Related]
12. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders. Molzer B; Kainz-Korschinsky M; Sundt-Heller R; Bernheimer H J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624 [TBL] [Abstract][Full Text] [Related]
13. Adrenoleukodystrophy with olivopontocerebellar atrophy-like lesions. Tateishi J; Sato Y; Suetsugu M; Takashiba T Clin Neuropathol; 1986; 5(1):34-9. PubMed ID: 3948452 [TBL] [Abstract][Full Text] [Related]
14. Polarizing inclusions in some organs of children with congenital peroxisomal diseases (Zellweger's, Refsum's, chondrodysplasia punctata (rhizomelic form), X-linked adrenoleukodystrophy). Kerckaert I; Dingemans KP; Heymans HS; Vamecq J; Roels F J Inherit Metab Dis; 1988; 11(4):372-86. PubMed ID: 2468818 [TBL] [Abstract][Full Text] [Related]
15. A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy. Mito T; Takada K; Akaboshi S; Takashima S; Takeshita K; Origuchi Y Acta Neuropathol; 1989; 77(4):437-40. PubMed ID: 2540612 [TBL] [Abstract][Full Text] [Related]