Literature DB >> 4448998

Muscle weakness after rest in myotonic disorders; an electrophysiological study.

J C Brown.   

Abstract

Changes in amplitude of the evoked muscle action potential (MAP) have been observed in four patients with myotonia congenita and two with dystrophia myotonica. A fade in the response occurred in every case with stimulus frequencies of 10 per second or less, provided that the muscle was in a rested state and that long enough stimulus trains were used. Intramuscular stimulation and recording techniques show that the myotonic muscle fibre is the site of this defect. The MAP fade is thought to represent the transient weakness from which such patients may suffer, particularly after rest. Since neither this weakness nor the fade was related to the severity of the myotonia, nor were they significantly influenced by cooling or hydantoins, they may well be due to a separate defect in the myotonic muscle from that which causes the hyperexcitability of the fibre membrane.

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Year:  1974        PMID: 4448998      PMCID: PMC1083649          DOI: 10.1136/jnnp.37.12.1336

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


  6 in total

1.  Studies in neuromuscular function. I. Introduction and methods.

Authors:  D GROB; A M HARVEY; R J JOHNS
Journal:  Bull Johns Hopkins Hosp       Date:  1956-09

2.  Therapy of myotonia. A double-blind evaluation of diphenylhydantoin, procainamide, and placebo.

Authors:  T L Munsat
Journal:  Neurology       Date:  1967-04       Impact factor: 9.910

3.  Paramyotonia congenita. Association with cutaneous cold sensitivity and description of peculiar sustained postures after muscle contraction.

Authors:  K R Magee
Journal:  Arch Neurol       Date:  1966-06

4.  The nature of the defect in the Eaton-Lambert syndrome.

Authors:  M P McQuillen; R J Johns
Journal:  Neurology       Date:  1967-06       Impact factor: 9.910

5.  [Neurophysiological studies on the temporary paresis in myotonia congenita and dystrophia myotonica].

Authors:  K Ricker; H M Meinch; H Stumpf
Journal:  Z Neurol       Date:  1973-04-02

6.  Electrophysiological study of dystrophia myotonica.

Authors:  A J McComas; M J Campbell; R E Sica
Journal:  J Neurol Neurosurg Psychiatry       Date:  1971-04       Impact factor: 10.154

  6 in total
  7 in total

1.  Physiological characterisation of the "warm up" effect of activity in patients with myotonic dystrophy.

Authors:  R G Cooper; M J Stokes; R H Edwards
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-09       Impact factor: 10.154

2.  Repetitive nerve stimulation in the differential diagnosis of congenital myotonia.

Authors:  B Rossi; A Rossi; F Sartucci
Journal:  Ital J Neurol Sci       Date:  1984-12

Review 3.  Clinical evaluation of membrane excitability in muscle channel disorders: potential applications in clinical trials.

Authors:  James C Cleland; Eric L Logigian
Journal:  Neurotherapeutics       Date:  2007-04       Impact factor: 7.620

4.  Transient muscular weakness in severe recessive myotonia congenita. Improvement of isometric muscle force by drugs relieving myotomic stiffness.

Authors:  K Ricker; A Haass; G Hertel; H G Mertens
Journal:  J Neurol       Date:  1978-08-25       Impact factor: 4.849

5.  Myotonia induced with clofibrate in rats.

Authors:  H Kwieciński
Journal:  J Neurol       Date:  1978-10-25       Impact factor: 4.849

6.  Myotonia not aggravated by cooling. Force and relaxation of the adductor pollicis in normal subjects and in myotonia as compared to paramyotonia.

Authors:  K Ricker; G Hertel; K Langscheid; G Stodieck
Journal:  J Neurol       Date:  1977-08-18       Impact factor: 4.849

7.  Myokymia and impaired muscular relaxation with continuous motor unit activity.

Authors:  F D Lublin; P Tsairis; L J Streletz; R A Chambers; W F Riker; A Van Poznak; S W Duckett
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-06       Impact factor: 10.154

  7 in total

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