Demyelinating hereditary neuropathies in

Publication:
Demyelinating hereditary neuropathies in

dc.contributor.author	Guzzetta, F.	es
dc.contributor.author	Guzzetta, A.	es
dc.contributor.author	Rodríguez, J.
dc.contributor.author	Deodato, M.
dc.contributor.author	Ferriere, G.
dc.date.accessioned	2011-02-22T10:29:36Z
dc.date.available	2011-02-22T10:29:36Z
dc.date.issued	1995
dc.description.abstract	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 critica1 pathological features emphasizing: 1) the variability of the recessive forms of HMSN; 2) the morphological distinction between HMSN type 1 and type 111; 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.	es
dc.format	application/pdf	es
dc.format.extent	14	es
dc.identifier.issn	0213-3911	es
dc.identifier.uri	http://hdl.handle.net/10201/18706
dc.language	eng	es
dc.publisher	Murcia : F. Hernández	es
dc.relation.ispartof	Histology and histopathology	es
dc.rights	info:eu-repo/semantics/openAccess	es
dc.subject	Child neuropathies	es
dc.subject	Hereditary neuropathies	es
dc.subject.other	CDU::6 - Ciencias aplicadas::61 - Medicina	es
dc.title	Demyelinating hereditary neuropathies in	es
dc.type	info:eu-repo/semantics/article	es
dspace.entity.type	Publication	es

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