Literature DB >> 8293177

Hereditary sensory neuropathies.

P K Thomas1.   

Abstract

Hereditary sensory neuropathies have not shared in the major advances that have taken place in the molecular genetics of the hereditary demyelinating motor and sensory neuropathies. Thus far, classification depends upon their mode of inheritance and clinical features. The delineation of the various clinical syndromes is still not complete. This is a necessary preliminary to establishing the genetic basis of these neuropathies. The hereditary sensory neuropathies can be accordingly grouped into those with predominantly sensory and some associated autonomic features and those in which a sensory neuropathy is part of a spinocerebellar degeneration or other multisystem degeneration.

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Year:  1993        PMID: 8293177     DOI: 10.1111/j.1750-3639.1993.tb00740.x

Source DB:  PubMed          Journal:  Brain Pathol        ISSN: 1015-6305            Impact factor:   6.508


  3 in total

1.  Hereditary sensory neuropathy type I: haplotype analysis shows founders in southern England and Europe.

Authors:  G A Nicholson; J L Dawkins; I P Blair; M Auer-Grumbach; S B Brahmbhatt; D J Hulme
Journal:  Am J Hum Genet       Date:  2001-07-27       Impact factor: 11.025

2.  Identification of dietary alanine toxicity and trafficking dysfunction in a Drosophila model of hereditary sensory and autonomic neuropathy type 1.

Authors:  Matthew C W Oswald; Ryan J H West; Emyr Lloyd-Evans; Sean T Sweeney
Journal:  Hum Mol Genet       Date:  2015-09-22       Impact factor: 6.150

Review 3.  Sphingolipid biosynthesis in man and microbes.

Authors:  Peter J Harrison; Teresa M Dunn; Dominic J Campopiano
Journal:  Nat Prod Rep       Date:  2018-09-19       Impact factor: 13.423

  3 in total

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