Literature DB >> 20983620

A familial peripheral neuropathy of unknown etiology resembling Morvan's disease.

M A OGRYZLO.   

Abstract

Entities:  

Keywords:  MORVAN'S DISEASE

Mesh：

Year:  1946        PMID： 20983620

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN： 0008-4409            Impact factor:   8.262


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  4 in total

1.  [The osteolysis syndrome].

Authors:  F SOMMER; K REINHARDT
Journal:  Arch Orthop Unfallchir       Date:  1959

Review 2.  Autonomic involvement in inherited neuropathies.

Authors:  P K Thomas
Journal:  Clin Auton Res       Date:  1992-02       Impact factor: 4.435

3.  Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.

Authors:  Ronald G Lafreniere; Marcia L E MacDonald; Marie-Pierre Dube; Julie MacFarlane; Mary O'Driscoll; Bernard Brais; Sebastien Meilleur; Ryan R Brinkman; Owen Dadivas; Terry Pape; Christele Platon; Chris Radomski; Jenni Risler; Jay Thompson; Ana-Maria Guerra-Escobio; Gudarz Davar; Xandra O Breakefield; Simon N Pimstone; Roger Green; William Pryse-Phillips; Y Paul Goldberg; H Banfield Younghusband; Michael R Hayden; Robin Sherrington; Guy A Rouleau; Mark E Samuels
Journal:  Am J Hum Genet       Date:  2004-04-01       Impact factor: 11.025

4.  WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio).

Authors:  Valérie Bercier; Edna Brustein; Meijiang Liao; Patrick A Dion; Ronald G Lafrenière; Guy A Rouleau; Pierre Drapeau
Journal:  PLoS Genet       Date:  2013-01-03       Impact factor: 5.917
  4 in total

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