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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study.

Twenty-three cases of hereditary demyelinating neuropathies are reported, 13 with different types of hereditary motor and sensory neuropathy (HMSN) and 9 with globoid cell or meta-chromatic leucodystrophies. Ultrastructural and morpho-metric studies showed some critical pathological features emphasizing: 1) the variability of the recessive forms of HMSN; 2) the morphological distinction between HMSN type I and type III; and 3) differences between these types of HMSN and other "onion bulb" neuropathies such as those found in leucodystrophies, which account for distinct underlying mechanisms.[1]

References

  1. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study. Guzzetta, F., Rodríguez, J., Deodato, M., Guzzetta, A., Ferrière, G. Histol. Histopathol. (1995) [Pubmed]
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