Literature DB >> 1155040

Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.

H B Szliwowski, P Drochmans.   

Abstract

The authors describe in biopsies from 6 cases of Werdnig-Hoffmann disease, including 2 of the more benign type, the ultrastructural typical aspects of denervation. They compare their findings with those of other workers. The striking points are the great variation in the diameter of the muscle fibres and the myofibrils, the disorganisation of the myofibrils, the sarcomeres and the filaments, with persistance of the relations between thick and thin filaments at various levels, the modifications of the Z-band and the triads in chains. The folds and the basement membrane are examined. Centrioles are present in a muscle fibre and in a satellite. Glycogen is very abundant. The nerves seem normal but some Schwann cells contain pi granules which are not observed usually at the age of the patient. The end plates and a muscle spindle are normal.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 1155040     DOI: 10.1007/bf00687923

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


  19 in total

1.  Infantile muscular atrophy.

Authors:  R K BYERS; B Q BANKER
Journal:  Arch Neurol       Date:  1961-08

2.  INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY.

Authors:  V DUBOWITZ
Journal:  Brain       Date:  1964-12       Impact factor: 13.501

3.  [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].

Authors:  S THIEFFRY; M ARTHUIS; E BARGETON
Journal:  Rev Neurol (Paris)       Date:  1955-10       Impact factor: 2.607

4.  An electron microscopic study of muscle in Werdnig-Hoffmann's disease.

Authors:  U van Haelst
Journal:  Virchows Arch A Pathol Pathol Anat       Date:  1970

5.  Infantile and juvenile spinal muscular atrophy.

Authors:  I Hausmanowa-Petrusewicz; W Askanas; B Badurska; B Emeryk; A Fidziańska; W Garbalińska; L Hetnarska; Z Kamieniecka; J Prot; I Niebrój-Dobosz; H Jedrzejowska; E Sawicka
Journal:  J Neurol Sci       Date:  1968 Mar-Apr       Impact factor: 3.181

6.  Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease.

Authors:  T L Munsat; R Woods; W Fowler; C M Pearson
Journal:  Brain       Date:  1969-03       Impact factor: 13.501

7.  Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis.

Authors:  A K Afifi; F P Aleu; J Goodgold; B MacKay
Journal:  Neurology       Date:  1966-05       Impact factor: 9.910

8.  Progressive spinal muscular atrophy with onset in infancy or early childhood.

Authors:  I Gamstorp
Journal:  Acta Paediatr Scand       Date:  1967-07

9.  Benign spinal muscular atrophy arising in childhood and adolescence.

Authors:  D Gardner-Medwin; P Hudgson; J N Walton
Journal:  J Neurol Sci       Date:  1967 Jul-Aug       Impact factor: 3.181

10.  [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].

Authors:  S BRANDT
Journal:  Nord Med       Date:  1950-09-15
View more
  4 in total

1.  Chronic progressive and relapsing neuromyopathy with massive dilatations of endoplasmic reticulum in muscle fibers.

Authors:  B Lach; S Christie; D Preston
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

2.  Nemaline bodies in a progressive infantile neuromuscular disorder.

Authors:  W de Coster; J de Reuck; H vander Eecken
Journal:  J Neurol       Date:  1978-09-12       Impact factor: 4.849

3.  A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle.

Authors:  T K Rajendra; Graydon B Gonsalvez; Michael P Walker; Karl B Shpargel; Helen K Salz; A Gregory Matera
Journal:  J Cell Biol       Date:  2007-03-12       Impact factor: 10.539

4.  Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy.

Authors:  Marc-Olivier Deguise; Justin G Boyer; Emily R McFall; Armin Yazdani; Yves De Repentigny; Rashmi Kothary
Journal:  Sci Rep       Date:  2016-06-28       Impact factor: 4.379

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.