Literature DB >> 4950913

Classification of neuromuscular disorders.

W K Engel.   

Abstract

Anew type of classification of neuromuscular diseases is presented. It is based on etiology; when this is not possible, on pathogenesis; if neither is possible, on distinctive features, biochemical greater than morphologic greater than clinical-genetic ones. The initial categorization designates which cell type, lower motor neuron or myofiber, is considered responsible for the major abnormality. This classification is designed to promote understanding of the pathogenesis and etiology of neuromuscular diseases in general and be applicable to a particular patient when the diagnostic studies are completed. It is not arranged as an approach to the initial differential diagnosis of a given patient.

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Year:  1971        PMID: 4950913

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  4 in total

1.  Diagnostic problems in (ocular) myasthenia.

Authors:  L A Bastiaensen; J H van Gasteren; C W Frenken; A C Leyten
Journal:  Doc Ophthalmol       Date:  1979-03-15       Impact factor: 2.379

2.  [Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Authors:  W Mortier; E Michaelis; J Becker; L Gerhard
Journal:  Humangenetik       Date:  1975

3.  Electromyographic findings in the so-called non-progressive myopathies.

Authors:  I Hausmanowa-Petrusewicz; B Ryniewicz
Journal:  J Neurol       Date:  1976-02-13       Impact factor: 4.849

4.  The perifascicular atrophy factor. An aid in the histological diagnosis of polymyositis.

Authors:  H P Baumli; M Mumenthaler
Journal:  J Neurol       Date:  1977-01-13       Impact factor: 4.849

  4 in total

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