Literature DB >> 4266590

Pathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease).

J T Hughes, B Brownell.   

Abstract

Four cases of peroneal muscular atrophy (Charcot-Marie-Tooth disease) are described in which observations were made from the necropsy examination of the central nervous system, the peripheral nervous system, and the skeletal muscles. The pattern of nerve degeneration in these various locations is described and the conclusion is drawn that the basis of the disease is a very chronic progressive neuropathy. To the pathological descriptions of previous observers is added the finding of fibrosis affecting the muscle spindles which was present in all four of the cases. The literature of the case reports with necropsy examination is reviewed.

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Mesh:

Year:  1972        PMID: 4266590      PMCID: PMC494144          DOI: 10.1136/jnnp.35.5.648

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  2 in total

1.  The spindle in normal and pathological muscle.

Authors:  A N Patel; V S Latitha; D K Dastur
Journal:  Brain       Date:  1968       Impact factor: 13.501

2.  The pathology of the muscle spindle. A study of biopsy material in various muscular and neuromuscular diseases.

Authors:  G Cazzato; J N Walton
Journal:  J Neurol Sci       Date:  1968 Jul-Aug       Impact factor: 3.181

  2 in total
  9 in total

1.  Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I.

Authors:  M Aramideh; J E Hoogendijk; C M Aalfs; F E Posthumus Meyjes; M De Visser; B W Ongerboer de Visser
Journal:  J Neurol       Date:  1992-05       Impact factor: 4.849

2.  The pathology of the lower leg muscles in pure forefoot pes cavus.

Authors:  T R Helliwell; M Tynan; M Hayward; L Klenerman; G Whitehouse; R H Edwards
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

3.  Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.

Authors:  P K Thomas; D B Calne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-01       Impact factor: 10.154

4.  Is the "cerebellar" incoordination of Refsum's disease due to structural lesions in the cerebellum?

Authors:  P Salisachs
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-05       Impact factor: 10.154

5.  An autopsy case of peroneal muscular atrophy with rigidity and tremor. Ultrastructural and systematic morphometrical studies on peripheral nerves.

Authors:  Y Itoh; S Yagishita; N Amano; K Iwabuchi
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

6.  Degeneration of anterior horn cell in neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II): a Golgi study.

Authors:  S Ono; K Hara; H Sasaki; I Sugano; K Nagao
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

7.  Texture analysis using T1-weighted images for muscles in Charcot-Marie-Tooth disease patients and volunteers.

Authors:  Ji Hyun Lee; Young Cheol Yoon; Hyun Su Kim; Jae-Hun Kim; Byung-Ok Choi
Journal:  Eur Radiol       Date:  2020-10-30       Impact factor: 5.315

8.  Dynamic aspects of peripheral nerve changes in progressive neural muscular atrophy: light- and electronmicroscopic studies of serial nerve biopsies.

Authors:  C Meier; R Maibach; W Isler; A Bischoff
Journal:  J Neurol       Date:  1976-01-14       Impact factor: 4.849

9.  Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.

Authors:  P Salisachs
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-12       Impact factor: 10.154

  9 in total

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