Literature DB >> 1121925

Ultrastructure of the syndrome of continuous muscle fibre activity.

H Sroka, B Bornstein, U Sandbank.   

Abstract

The ultrastructure of muscle and the myoneural junction of a man of 60 suffering from the syndrome of continuous muscle fibre activity was studied. This syndrome is manifested by disturbances of walking, muscle weakness, permanent muscle contractions and involuntary movements. The myoneural junction was hypertrophied and showed ramifications of the secondary clefts. The presynaptic nerve ending contained no synaptic vesicles. The relationship of these findings to the disease is discussed.

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Year:  1975        PMID: 1121925     DOI: 10.1007/bf00696889

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  14 in total

1.  A SYNDROME OF CONTINUOUS MUSCLE-FIBRE ACTIVITY.

Authors:  H Isaacs
Journal:  J Neurol Neurosurg Psychiatry       Date:  1961-11       Impact factor: 10.154

2.  Histometric study of neuromuscular junction ultrastructure. II. Myasthenic syndrome.

Authors:  T Santa; A G Engel; E G Lambert
Journal:  Neurology       Date:  1972-04       Impact factor: 9.910

3.  The intramuscular nerve endings in dystrophia myotonica--a biopsy study by vital staining and electron microscopy.

Authors:  D E Allen; A G Johnson; A L Woolf
Journal:  J Anat       Date:  1969-07       Impact factor: 2.610

4.  Ultrastructural alterations of the motor end plate in myotonic dystrophy of the mouse (dy2J dy2J).

Authors:  J J Gilbert; M C Steinberg; B Q Banker
Journal:  J Neuropathol Exp Neurol       Date:  1973-07       Impact factor: 3.685

5.  An electron microscopic study of the changes induced by botulinum toxin in the motor end-plates of slow and fast skeletal muscle fibres of the mouse.

Authors:  L W Duchen
Journal:  J Neurol Sci       Date:  1971-09       Impact factor: 3.181

6.  Pseudo-myotonia and myokymia.

Authors:  R C Hughes; W B Matthews
Journal:  J Neurol Neurosurg Psychiatry       Date:  1969-02       Impact factor: 10.154

7.  Ultrastructural changes in the motor nerve terminals caused by beta-bungarotoxin.

Authors:  I L Chen; C Y Lee
Journal:  Virchows Arch B Cell Pathol       Date:  1970

8.  [Neuromyotonia].

Authors:  H G Mertens; S Zschocke
Journal:  Klin Wochenschr       Date:  1965-09-01

9.  Continuous muscle fibre activity in an Indian male with additional evidence of terminal motor fibre abnormality.

Authors:  H Isaacs
Journal:  J Neurol Neurosurg Psychiatry       Date:  1967-04       Impact factor: 10.154

10.  Changes in the fine structure of the neuromuscular junction of the frog caused by black widow spider venom.

Authors:  A W Clark; W P Hurlbut; A Mauro
Journal:  J Cell Biol       Date:  1972-01       Impact factor: 10.539

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  3 in total

1.  The syndrome of continuous muscle fibre activity: light and electron microscopic studies in muscle and nerve biopsies.

Authors:  S Ono; S Munakata; K Nagao; N Shimizu; N Shimizu
Journal:  J Neurol       Date:  1989-10       Impact factor: 4.849

2.  Neuromuscular, autonomic and central cholinergic hyperactivity associated with thymoma and acetylcholine receptor-binding antibody.

Authors:  M Halbach; V Hömberg; H J Freund
Journal:  J Neurol       Date:  1987-08       Impact factor: 4.849

3.  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

  3 in total

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