Literature DB >> 4285163

Hereditary compression syndrome of peripheral nerves.

A Staal, C J de Weerdt, L N Went.   

Abstract

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Year:  1965        PMID： 4285163     DOI： 10.1212/wnl.15.11.1008

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  8 in total

1.  Recurrent familial neuropathy with liability to pressure palsies: reports of two cases and ultrastructural nerve study.

Authors:  J Dubi; F Regli; A Bischoff; C Schneider; G de Crousaz
Journal:  J Neurol       Date:  1979-01-30       Impact factor: 4.849

2.  Visual and somatosensory evoked potentials and F-wave latency measurements in hereditary neuropathy with liability to pressure palsies.

Authors:  H Strenge; D Soyka; W Tackmann
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

3.  Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy.

Authors:  K Adlkofer; R Frei; D H Neuberg; J Zielasek; K V Toyka; U Suter
Journal:  J Neurosci       Date:  1997-06-15       Impact factor: 6.167

4.  DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

Authors:  K Silander; P Halonen; R Sara; H Kalimo; B Falck; M L Savontaus
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-10       Impact factor: 10.154

5.  Clinical spectrum of the tomaculous neuropathies. Report of 60 cases and review of the literature.

Authors:  N Rizzuto; G Moretto; S Galiazzo Rizzuto
Journal:  Ital J Neurol Sci       Date:  1993-12

6.  Hereditary neuropathy with liability to pressure palsies. Report of two families and review of the literature.

Authors:  C Meier; C Moll
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

7.  Recurrent familial neuropathy due to liability to pressure palsies.

Authors:  R Marazzi; D Pareyson; V Scaioli; M Corbo; A Boiardi; G Chiodelli; A Sghirlanzoni
Journal:  Ital J Neurol Sci       Date:  1988-08

8.  Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.

Authors:  Bo Yuan; Juanita Neira; Shen Gu; Tamar Harel; Pengfei Liu; Ignacio Briceño; Sarah H Elsea; Alberto Gómez; Lorraine Potocki; James R Lupski
Journal:  Hum Genet       Date:  2016-07-07       Impact factor: 4.132
  8 in total

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