Literature DB >> 55468

Histochemistry and electron microscopy of muscle fibres in a case of congenital paramyotonia.

D Schiffer, M T Giordana, G Monga, F Mollo.   

Abstract

In a case of congenital paramyotonia a muscle biopsy was performed and studied morphologically, histochemically and ultrastructurally. A clearcut pattern of changes has been observed with ATPase and oxidative enzymes. On electron microscopy special changes known as "tubular aggregates" were found. The relationship between the two findings, as well as the significance of such alterations in the range of periodic paralyses and myotonic phenomena, are discussed.

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Year:  1976        PMID： 55468     DOI： 10.1007/bf00313356

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


  27 in total

1.  [Not Available].

Authors:  I GAMSTORP
Journal:  Acta Paediatr Suppl       Date:  1956-05

2.  [Clinical, morphological, histochemical and ultrastructural studies in a case of myopathy with tubular aggregations].

Authors:  M T Giordana; D Schiffer; L Fra; G Monga; F Mollo
Journal:  Acta Neurol (Napoli)       Date:  1974 Jul-Aug

3.  Biochemical abnormalities of muscle ribosomes during attacks of hyperkalemic periodic paralysis.

Authors:  V Ionasescu; H Zellweger; S S Schochet; T W Conway
Journal:  J Neurol Sci       Date:  1973-08       Impact factor: 3.181

4.  Tubular aggregates in type II muscle fibers: ultrastructural and histochemical correlation.

Authors:  W K Engel; D W Bishop; G G Cunningham
Journal:  J Ultrastruct Res       Date:  1970-06

5.  The myopathy of hyperkalemic periodic paralysis. An electron microscopic study.

Authors:  R D Macdonald; N B Rewcastle; J G Humphrey
Journal:  Arch Neurol       Date:  1968-09

6.  A light and electron microscopic study of a second case of hypokalemic periodic paralysis with hyperthyroidism.

Authors:  L M Dunkle; C H Diggs; R A Bergman; R J Johns
Journal:  Johns Hopkins Med J       Date:  1970-04

7.  Hypokalemic periodic paralysis. Children with permanent myopathic weakness.

Authors:  M Dyken; W Zeman; T Rusche
Journal:  Neurology       Date:  1969-07       Impact factor: 9.910

8.  Adynamia episodica hereditaria. Clinical, pathological and electrophysiological studies in an affected family.

Authors:  W G Bradley
Journal:  Brain       Date:  1969       Impact factor: 13.501

9.  Familial hypokalemic periodic paralysis with permanent myopathy. A clinical and ultrastructural study.

Authors:  D L Odor; A N Patel; L A Pearce
Journal:  J Neuropathol Exp Neurol       Date:  1967-01       Impact factor: 3.685

10.  Hyperkalemic periodic paralysis.

Authors:  R B Layzer; R E Lovelace; L P Rowland
Journal:  Arch Neurol       Date:  1967-05
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  1 in total

1.  Tubular aggregates: their association with myalgia.

Authors:  E Niakan; Y Harati; M J Danon
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-09       Impact factor: 10.154
  1 in total

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