Literature DB >> 8344020

Hereditary motor and sensory neuropathies. Present status of types I, II and III.

A A Gabreëls-Festen1, F J Gabreëls, F G Jennekens.   

Abstract

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Mesh：

Year:  1993        PMID： 8344020     DOI： 10.1016/0303-8467(93)90002-x

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN： 0303-8467            Impact factor:   1.876


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  4 in total

1.  A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Authors:  A Bouhouche; A Benomar; N Birouk; A Mularoni; F Meggouh; J Tassin; D Grid; A Vandenberghe; M Yahyaoui; T Chkili; A Brice; E LeGuern
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  Decreased electrical excitability of peripheral nerves in demyelinating polyneuropathies.

Authors:  J Meulstee; A Darbas; P A van Doorn; L van Briemen; F G van der Meché
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-04       Impact factor: 10.154

Review 3.  Molecular anatomy and genetics of myelin proteins in the peripheral nervous system.

Authors:  G J Snipes; U Suter
Journal:  J Anat       Date:  1995-06       Impact factor: 2.610

Review 4.  PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.

Authors:  Barbara W van Paassen; Anneke J van der Kooi; Karin Y van Spaendonck-Zwarts; Camiel Verhamme; Frank Baas; Marianne de Visser
Journal:  Orphanet J Rare Dis       Date:  2014-03-19       Impact factor: 4.123
  4 in total

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