These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
230 related articles for article (PubMed ID: 7507276)
1. Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders. Hughes JL; Crane DI; Robertson E; Poulos A Virchows Arch A Pathol Anat Histopathol; 1993; 423(6):459-68. PubMed ID: 7507276 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect. Guerroui S; Aubourg P; Chen WW; Hashimoto T; Scotto J Biochem Biophys Res Commun; 1989 May; 161(1):242-51. PubMed ID: 2471528 [TBL] [Abstract][Full Text] [Related]
4. 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]
6. 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]
7. Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data. Roels F; Pauwels M; Poll-Thé BT; Scotto J; Ogier H; Aubourg P; Saudubray JM Virchows Arch A Pathol Anat Histopathol; 1988; 413(4):275-85. PubMed ID: 3140473 [TBL] [Abstract][Full Text] [Related]
8. Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells. Yajima S; Suzuki Y; Shimozawa N; Yamaguchi S; Orii T; Fujiki Y; Osumi T; Hashimoto T; Moser HW Hum Genet; 1992 Mar; 88(5):491-9. PubMed ID: 1372585 [TBL] [Abstract][Full Text] [Related]
9. Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome. van Roermund CW; Brul S; Tager JM; Schutgens RB; Wanders RJ J Inherit Metab Dis; 1991; 14(2):152-64. PubMed ID: 1679469 [TBL] [Abstract][Full Text] [Related]
10. [Peroxisomes and peroxisomal diseases]. Petelenz M; Gonciarz Z; Grzybek H; Panz B Postepy Hig Med Dosw; 1991; 45(1-2):77-99. PubMed ID: 1717967 [TBL] [Abstract][Full Text] [Related]
11. Investigation of peroxisomal lipid beta-oxidation enzymes in guinea pig liver peroxisomes by immunoblotting and immunocytochemistry. Yamamoto K; Völkl A; Fahimi HD J Histochem Cytochem; 1992 Dec; 40(12):1909-18. PubMed ID: 1360481 [TBL] [Abstract][Full Text] [Related]
12. Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease. Schram AW; Strijland A; Hashimoto T; Wanders RJ; Schutgens RB; van den Bosch H; Tager JM Proc Natl Acad Sci U S A; 1986 Aug; 83(16):6156-8. PubMed ID: 2426710 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group. Wiemer EA; Out M; Schelen A; Wanders RJ; Schutgens RB; Van den Bosch H; Tager JM Biochim Biophys Acta; 1991 Oct; 1097(3):232-7. PubMed ID: 1718439 [TBL] [Abstract][Full Text] [Related]
14. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy). Poll-The BT; Roels F; Ogier H; Scotto J; Vamecq J; Schutgens RB; Wanders RJ; van Roermund CW; van Wijland MJ; Schram AW Am J Hum Genet; 1988 Mar; 42(3):422-34. PubMed ID: 2894756 [TBL] [Abstract][Full Text] [Related]
15. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease. Singh I; Voigt RG; Sheikh FG; Kremser K; Brown FR Biochem Mol Med; 1997 Aug; 61(2):198-207. PubMed ID: 9259985 [TBL] [Abstract][Full Text] [Related]
16. Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders. Poll-The BT; Skjeldal OH; Stokke O; Poulos A; Demaugre F; Saudubray JM Hum Genet; 1989 Jan; 81(2):175-81. PubMed ID: 2463966 [TBL] [Abstract][Full Text] [Related]
17. Human liver pathology in peroxisomal diseases: a review including novel data. Roels F; Espeel M; Poggi F; Mandel H; van Maldergem L; Saudubray JM Biochimie; 1993; 75(3-4):281-92. PubMed ID: 7685191 [TBL] [Abstract][Full Text] [Related]
18. Infantile Refsum's disease: a generalized peroxisomal disorder. Case report with postmortem examination. Torvik A; Torp S; Kase BF; Ek J; Skjeldal O; Stokke O J Neurol Sci; 1988 May; 85(1):39-53. PubMed ID: 2455020 [TBL] [Abstract][Full Text] [Related]
19. [Neuropathology of peroxisomal disorders; Zellweger syndrome and neonatal adrenoleukodystrophy]. Takashima S; Houdou S; Kamei J; Hasegawa M; Mito T; Suzuki Y; Maeda K No To Hattatsu; 1992 Mar; 24(2):186-93. PubMed ID: 1567656 [TBL] [Abstract][Full Text] [Related]