Literature DB >> 4013678

Ultrastructural studies on the neuromuscular junctions of Becker's muscular dystrophy.

N Fukuhara, M Suzuki, T Tsubaki, S Kushiro, N Takasawa.   

Abstract

Ultrastructural studies on muscle biopsies from three patients with Becker's muscular dystrophy showed that the i.m. nerves presented loss or disarrangement of the neurofilaments and an increased number of glycogen granules and/or myelin figures not infrequently in the myelinated and unmyelinated nerve fibers. The neuromuscular junctions showed markedly widened sole-plate areas, and several terminal axons frequently abutted and formed neuromuscular junctions on the same fiber. The secondary synaptic clefts were markedly decreased in number and short in length in type I fibers but not in type II fibers. Most terminal axons showed no degenerative changes. Therefore, the participation of a neural factor might be suggested as the cause of Becker's muscular dystrophy, although it does not mean denervation in the conventional sense of an axonal degeneration.

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Year:  1985        PMID: 4013678     DOI: 10.1007/bf00690960

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


  29 in total

1.  Duchenne dystrophy: ultrastructural localization of the acetylcholine receptor and intracellular microelectrode studies of neuromuscular transmission.

Authors:  H Sakakibara; A G Engel; E H Lambert
Journal:  Neurology       Date:  1977-08       Impact factor: 9.910

2.  New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

Authors:  M Zatz; S B Itskan; R Sanger; O Frota-Pessoa; P H Saldanha
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

3.  Duchenne dystrophy. II. Morphometric study of motor end-plate fine structure.

Authors:  F Jerusalem; A G Engel; M R Gomez
Journal:  Brain       Date:  1974-03       Impact factor: 13.501

4.  Z- and M-band appearance in different histochemically defined types of human skeletal muscle fibers.

Authors:  M Sjöström; S Kidman; K H Larsén; K A Angquist
Journal:  J Histochem Cytochem       Date:  1982-01       Impact factor: 2.479

5.  The fine structural differences in human muscle fiber types based on peroxidatic activity.

Authors:  L M Saltis; J R Mendell
Journal:  J Neuropathol Exp Neurol       Date:  1974-10       Impact factor: 3.685

6.  A comparison of the fine structure of motor end-plates in Duchenne dystrophy and in human neurogenic diseases.

Authors:  D G Harriman
Journal:  J Neurol Sci       Date:  1976-06       Impact factor: 3.181

7.  Becker-type muscular dystrophy.

Authors:  W G Bradley; M Z Jones; J M Mussini; P R Fawcett
Journal:  Muscle Nerve       Date:  1978 Mar-Apr       Impact factor: 3.217

8.  Morphometric analyses of human muscle fiber types.

Authors:  M Sjöström; K A Angquist; A C Bylund; J Fridén; L Gustavsson; T Scherstén
Journal:  Muscle Nerve       Date:  1982-09       Impact factor: 3.217

9.  Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

Authors:  H M Kingston; N S Thomas; P L Pearson; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

10.  Electron microscope study of the human neuromuscular junction.

Authors:  E DE HARVEN; C COERS
Journal:  J Biophys Biochem Cytol       Date:  1959-08
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  3 in total

1.  Muscle damage induced by isotretinoin.

Authors:  E Hodak; N Gadoth; M David; M Sandbank
Journal:  Br Med J (Clin Res Ed)       Date:  1986-08-16

2.  Neuromuscular junctions (NMJs): ultrastructural analysis and nicotinic acetylcholine receptor (nAChR) subunit mRNA expression in offspring subjected to protein restriction throughout pregnancy.

Authors:  Paula Aiello Tomé de Souza Castro; Ludimila Canuto Faccioni; Patrícia Aline Boer; Robson Francisco Carvalho; Selma Maria Michelin Matheus; Maeli Dal-Pai-Silva
Journal:  Int J Exp Pathol       Date:  2017-05-25       Impact factor: 1.925

3.  Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies.

Authors:  Massimo Ganassi; Peter S Zammit
Journal:  Eur J Transl Myol       Date:  2022-03-18
  3 in total

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