Literature DB >> 212921

Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome.

J C Brust, R E Lovelace, S Devi.   

Abstract

Entities:  

Mesh：

Year:  1978        PMID： 212921

Source DB:  PubMed          Journal:  Acta Neurol Scand Suppl        ISSN： 0065-1427


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  13 in total

1.  Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).

Authors:  C Weiller; A Ferbert
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

Review 2.  Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Authors:  D Pareyson; V Scaioli; M Laurà
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

Review 3.  Investigation of peripheral neuropathy.

Authors:  J G McLeod
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-03       Impact factor: 10.154

4.  Peroneal muscular atrophy with pyramidal features.

Authors:  A E Harding; P K Thomas
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-02       Impact factor: 10.154

5.  Genetic aspects of hereditary motor and sensory neuropathy (types I and II).

Authors:  A E Harding; P K Thomas
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

6.  Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Authors:  F L Mastaglia; K J Nowak; R Stell; B A Phillips; J E Edmondston; S M Dorosz; S D Wilton; J Hallmayer; B A Kakulas; N G Laing
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-08       Impact factor: 10.154

Review 7.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

8.  Pattern shift visual evoked potentials in Charcot-Marie-Tooth disease, HMSN type I.

Authors:  W Tackmann; E W Radü
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

9.  Distal and scapuloperoneal distributions of muscle involvement occurring within a family with type I hereditary motor and sensory neuropathy.

Authors:  A E Harding; P K Thomas
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

10.  Hereditary motor and sensory neuropathies: a genetic and epidemiological study in the province of Turin, Italy.

Authors:  A Chiò; A Tribolo; F Brignolio; M Leone; P Meineri; M G Rosso; M Mostert; D Schiffer
Journal:  Ital J Neurol Sci       Date:  1987-08
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