Literature DB >> 11073363

Classification of the hereditary motor and sensory neuropathies.

M M Reilly1.   

Abstract

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Year:  2000        PMID： 11073363     DOI： 10.1097/00019052-200010000-00009

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN： 1350-7540            Impact factor:   5.710


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  8 in total

Review 1.  Peripheral neuropathy.

Authors:  Richard A C Hughes
Journal:  BMJ       Date:  2002-02-23

Review 2.  Genetic neuromuscular disease.

Authors:  Mary M Reilly; Michael G Hanna
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-12       Impact factor: 10.154

Review 3.  Neurology and orthopaedics.

Authors:  Henry Houlden; Paul Charlton; Dishan Singh
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-03       Impact factor: 10.154

Review 4.  New insights into the pathophysiology of pes cavus in Charcot-Marie-Tooth disease type 1A duplication.

Authors:  José Berciano; Elena Gallardo; Antonio García; Ana L Pelayo-Negro; Jon Infante; Onofre Combarros
Journal:  J Neurol       Date:  2011-05-18       Impact factor: 4.849

Review 5.  Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.

Authors:  Henry Houlden; Mary M Reilly
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

6.  Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

Authors:  Annachiara De Sandre-Giovannoli; Malika Chaouch; Serguei Kozlov; Jean-Michel Vallat; Meriem Tazir; Nadia Kassouri; Pierre Szepetowski; Tarik Hammadouche; Antoon Vandenberghe; Colin L Stewart; Djamel Grid; Nicolas Lévy
Journal:  Am J Hum Genet       Date:  2002-01-17       Impact factor: 11.025

Review 7.  Role of immune cells in animal models for inherited neuropathies: facts and visions.

Authors:  Mathias Mäurer; Igor Kobsar; Martin Berghoff; Christoph D Schmid; Stefano Carenini; Rudolf Martini
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

8.  Investigation of Mutations in Exon 14 of SH3TC2 Gene and Exon 7 of NDRG1 Gene in Iranian Charcot-Marie-Tooth Disease Type 4 (CMT4D) Patients.

Authors:  Rahmaneh Sadat Moosavi; Niloofar Jahangir Sooltani; Massoud Houshmand
Journal:  Iran J Child Neurol       Date:  2020
  8 in total

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