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Ultrastructural Pathology Volume 14, 1990 - Issue 6
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Original Article

An Atypical Ultrastructural Pattern in Fabry's Disease: A Study on Its Nature and Incidence in 7 Cases

M. Elleder 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
,
J. Ledvinová 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
,
F. Vosmik 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
,
J. Zeman 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
,
D. Stejskal 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
&
A. Lageron 1st Institute of Pathology, Laboratory for Proteosynthesis, 2nd Dermatological Clinic, 4th Paediatric Clinic, School of Medicine, Charles University, Middle Bohemia District, Department of Medical Genetics, Prague, Czechoslovakia; Biochemical Laboratory, C.H.U. Saint-Antoine, Paris, France
Pages 467-474 | Accepted 03 May 1990, Published online: 10 Jul 2009

References

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  • Perrelet A, Forssmann W G, Franceschetti A Th, Rouiller C h. A study of Fabry's disease. II. Light and electron microscopy. Dermatologica 1969; 138: 222–237
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  • Dvorak A M, Cable W JL, Osage J E, Kolodny E H. Diagnostic electron microscopy II. Fabry's disease: Use of biopsies from uninvolved skin. Acute and chronic changes involving the microvasculature and small unmyelinated nerves. Pathology Annual, S C Summers, P P Rosen. Appleton-Century-Crofts, New York 1981; vol. 16: 139–158, pt 1
  • Vital A, Vital C, Maleville J. Fabry's disease: an ultrastructural study of muscle and peripheral nerve. Clin Neuropathol 1984; 3: 168–172
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  • Lillie R D, Fullmer H M. Histopathologic technique and practical histochemistry, 4th ed. McGraw-Hill, New York 1976
  • Esselman W J, Laine R A, Sweeley C C. Isolation and characterization of glycosphingolipids. M Enzymol 1972; 28: 140–156
  • Elleder M, Stejskal J. Induction of dipeptidylpeptidase IV activity in human renal glomeruli-A histochemical study. Acta Histochem (Jena) 1985; 77: 75–78
  • Wherrett J R, Hakomori S-I. Characterization of a blood group B glycolipid, accumulating in the pancreas of a patient with Fabry's disease. J Biol Chem 1973; 218: 3046–3051
  • Alroy J, Ucci A A, Pereira M EA. Lectins: Histochemical probes for specific carbohydrate residue. Advances in immunohistochemistry, R A DeLellis. Masson Inc., New York 1984; 67–88
  • Dean K J, Sweeley C C. Fabry disease. Practical Enzymology of Sphingolipidoses, R H Glew, S P Peters. Alan R. Liss, New York 1977; 174–216

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