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Neuroaxonal Dystrophy

Keywords

Myenteric Plexus Autosomal Recessive Disease Eccrine Sweat Gland Axonal Dystrophy Axon Demyelination 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. De Leon G, and Mitchel M (1985) Histological and ultrastructural features of dystrophic isocortical axons in infantile neuroaxonal dystrophy (Seitelberger’s disease). Acta Neuropathol (Berlin) 66: 89CrossRefPubMedGoogle Scholar
  2. Desnick R, and Schindler D (2001). α-N-acetylgalactosaminidase deficiency: Schindler’s disease. In: The metabolic and molecular bases of inherited disease (Scriver C, Beaudet A, Valle D, Sly WS, Childs B, Kinzler K, and Vogelstein B, eds). New York: McGraw-Hill, pp 3483Google Scholar
  3. Kanzaki T, Wang A, and Desnick R (1991) Lysosomal α-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria. J Clin Invest 88: 707PubMedGoogle Scholar
  4. Schindler D, Bishop DF, Wolfe D, Wang A, Egge H, Lemieux R, and Desnick R (1989) Neuroaxonal dystrophy due to lysosomal α-N-acetylgalactosaminidase deficiency. N Engl J Med 320: 1735PubMedGoogle Scholar
  5. Schröder J (2001) Pathology of Peripheral Nerves. An atlas of structural and molecular pathological changes. Berlin: SpringerGoogle Scholar
  6. Walkey S, Baker H, Rattazzi M, Haskins M, and Wu J-Y (1991) Neuroaxonal dystrophy in neuronal storage disorders: Evidence for major GABAergic neuron involvement. J Neurol Sci 104: 1CrossRefPubMedGoogle Scholar
  7. Wolfe D, Schindler D, and Desnick R (1995) Neuroaxonal dystrophy in infantile α-N-acetylgalactosaminidase deficiency. J Neurol Sci 132: 44CrossRefPubMedGoogle Scholar

Copyright information

© Springer-Verlag/Wien 2005

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