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Polarizing Inclusions in Some Organs of Children With Congenital Peroxisomal Diseases (zellwegers, Refsums, Chondrodysplasia Punctata (rhizomelic Form), X-linked Adrenoleukodystrophy)

  1. Barth, P. G., Schutgens, R. B. H., Bakkeren, J. A. J. M., Dingemans, K. P., Heymans, H. S. A., Douwes, A. C. and Van der Klei-van Moorsel, J. M. A milder variant of Zellweger syndrome.Eur. J. Pediatr. 144 (1985) 338–342
  2. Bremer, J. and Norum, K. R. Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet.J. Lipid Res. 23 (1982) 243–256
  3. Christiansen, R. Z., Osmundsen, H., Borrebaek, B. and Bremer, J. The effects of clofibrate feeding on the metabolism of palmitate and erucate in isolated hepatocytes.Lipids 13 (1978) 487–491
  4. Ghatak, N. R., Nochlin, D., Peris, M. and Myer, E. C. Morphology and distribution of cytoplasmic inclusions in adrenoleukodystrophy.J. Neurol. Sci. 50 (1981) 391–398
  5. Gilchrist, K. W., Gilbert, E. F., Goldfarb, S., Goll, U., Spranger, J. W. and Opitz, J. M. Studies of malformation syndromes of man. XI B: The cerebro-hepato-renal syndrome of Zellweger: comparative pathology.Eur. J. Pediatr. 121 (1976) 99–118
  6. Heymans, H. S. A., Van den Bosch, H., Schutgens, R. B. H., Tegelaers, W. H. H., Walther, J. U., Müller-Höcker, J. and Borst, P. Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.Eur. J. Pediatr. 142 (1984) 16–20
  7. Heymans, H. S. A., Oorthuys, J. W. E., Nelck, G., Wanders, R. J. A., Dingemans, K. P. and Schutgens, R. B. H. Peroxisomal abnormalities in rhizomelic chondrodysplasia punctata.J. Inher. Metab. Dis. 9 (1986) 329–331
  8. Johnson A B, Schaumburg H H, Powers J M, Histochemical characteristics of the striated inclusions of adrenoleukodystrophy., 10.1177/24.6.59773
  9. Kerckaert, I., Dingemans, K. P., Heymans, H. S. A., Vamecq, J., Poll-The, B. T., Van den Branden, C. and Roels, F. Polarizing inclusions in the liver of children with congenital peroxisomal diseases (syndrome of Zellweger; infantile Refsum's disease; chondrodysplasia punctata).Eur. J. Cell. Biol. 41, suppl. 14 (1986a) 22
  10. Kerckaert, I., Dingemans, K. P., Heymans, H. S. A., Vamecq, J., Poll-The, B. T. and Roels, F. Polarizing inclusions in the liver of children with congenital peroxisomal diseases (syndrome of Zellweger; infantile Refsum's disease; chondrodysplasia punctata).Hepat. Rapid Lit. Rev. 16-6 (1986b) 1911
  11. Lison, H. InHistochemie et Cytochemie Animales — Vol II. Gauthiers-Villars, Paris, 1960, p. 486.
  12. Mooi, W. J., Dingemans, K. P., van den Bergh-Weerman, M. A., Jöbsis, A. C., Heymans, H. S. A. and Barth, P. G. Ultrastructure of the liver in the cerebro-hepato-renal syndrome of Zellweger.Ultrastruct. Pathol. 5 (1983) 135–144
  13. Pearse, A. G. E. InHistochemistry: Theoretical and Applied (3th edition) Volume I. Little, Brown & Company, Boston, 1968, pp. 264, 460–467, 706–708
  14. Partin, J. S. and McAdams, A. J. Absence of hepatic peroxisomes in neonatal onset adrenoleukodystrophy.Pediatr. Res. 17 (1983) 294A
  15. Poulos, A., Pollard, A. C., Mitchell, J. G., Wise, G. and Mortimer, G. Patterns of Refsum's disease. Phytanic acid oxidase deficiency.Arch. Dis. Child. 59 (1984) 222–229
  16. Pretorius, P. J., Reinecke, C. J. and Op't Hof, J. Biochemical evidence for clinically diagnosed adrenoleukodystrophy in two brothers.S.A. Med. J. 65 (1984) 860–862
  17. Roels, F., Cornelis, A., Poll-The, B. T., Aubourg, P., Ogier, H., Scotto, J. and Saudubray, J. M. Hepatic peroxisomes are deficient in infantile Refsum's disease. A cytochemical study of 4 cases.Am. J. Med. Genet. 25 (1986) 257–271
  18. Roels, F., Pauwels, M., Poll-The, B. T., Scotto, J., Ogier, H., Aubourg, P. and Saudubray, J. M. Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: Cytochemical and morphometric data.Virchows Archiv A (1988) (in press)
  19. Schutgens, R. B. H., Romeyn, G. J., Wanders, R. J. A., Van den Bosch, H., Schrakamp, G. and Heymans, H. S. A. Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in fibroblasts from patients with cerebro-hepato-renal (Zellweger) syndrome.Biochem. Biophys. Res. Commun. 120 (1984) 179–184
  20. Schutgens, R. B. H., Heymans, H. S. A., Wanders, R. J. A., Van den Bosch, H. and Tager, J. M. Peroxisomal disorders: a newly recognised group of genetic diseases.Eur. J. Pediatr. 144 (1986) 430–440
  21. Scotto, J. M., Hadchouel, M., Odièvre, M., Laudat, M-H., Saudubray, J. M., Dulac, C., Beucler, I. and Beaune, P. Infantile phytanic acid storage disease, a possible variant of Refsum's disease: 3 cases, including ultrastructural studies of the liver.J. Inher. Metab. Dis. 5 (1982) 83–90
  22. Snedecor, G. W. and Cochran, W. G. Shortcut and non-parametric methods. InStatistical Methods (6th edition), The Iowa State University Press, Ames, Iowa, USA, 1967, p. 131
  23. Spurr, A. R. A low-viscosity epoxy resin embedding medium for electron microscopy.J. Ultrastruct. Res. 26 (1969) 31–43
  24. Vamecq, J., Draye, J. P., Van Hoof, F., Misson, J. P., Evrard, P., Verellen, G., Eyssen, H. J., Van Eldere, J., Schutgens, R. B. H., Wanders, R. J. A., Roels, F. and Goldfischer, S. L. Multiple peroxisomal enzymatic deficiency disorders: a comparative biochemical and morphologic study of Zellweger cerebro-hepato-renal syndrome and neonatal adrenoleukodystrophy.Am. J. Pathol. 125 (1986) 524–535
Bibliographic reference Kerckaert, I. ; Dingemans, KP. ; Heymans, HSA. ; Vamecq, J. ; Roels, F.. Polarizing Inclusions in Some Organs of Children With Congenital Peroxisomal Diseases (zellwegers, Refsums, Chondrodysplasia Punctata (rhizomelic Form), X-linked Adrenoleukodystrophy). In: Journal of Inherited Metabolic Disease, Vol. 11, no. 4, p. 372-386 (1988)
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