Fabry’s Disease


Fabry Disease Dermal Papilla Smooth Muscle Fibre Fabry Disease Patient Mitral Valve Insufficiency 
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  1. Cable WJ, Dvorak AM, Osage JE, and Kolodny EH (1982) Fabry’s disease: significance of ultrastructural localisation of lipid inclusions in dermal nerves. Neurology 32: 347PubMedGoogle Scholar
  2. Desnick R, Ioannou Y, and Eng C (2001 α-galactosidase A deficiency: Fabry’s disease. In: The metabolic and molecular bases of inherited disease (Scriver C, Beaudet A, Sly W, and Valle D, eds). New York: McGraw-Hill, pp 3733Google Scholar
  3. Faraggiana T, Churg J, Grishman E, Strauss L, Prado A, Bishop DF, Schuchman E, and Desnick RJ (1981) Light-and electron-microscopic histochemistry of Fabry’s disease. Am J Pathol 103: 247PubMedGoogle Scholar
  4. Roth J, Schulze E, Raabe G, and Waldmann G (1974) Analytische Studie des Morbus Fabry. Virchows Arch A Path Anat 363: 287CrossRefGoogle Scholar
  5. Schatzki PF, Kipreos B, and Payne J (1979) Fabry’s disease. Primary diagnosis by electron microscopy. Am J Surg Pathol 3: 211PubMedGoogle Scholar
  6. Uchino M, Uyama E, Kawano H, Hokamaki J, Kugiyama K, Murakami Y, Yasue H, and Ando M (1995) A histochemical and electron microscopic study of skeletal and cardiac muscle from a Fabry disease patient and carrier. Acta Neuropathol (Berlin) 90: 334PubMedGoogle Scholar

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© Springer-Verlag/Wien 2005

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