Literature DB >> 7271245

Preservation of the phrenic motoneurons in Werdnig-Hoffmann disease.

S Kuzuhara, S M Chou.   

Abstract

A neuropathological study on spinal cords at the third, fourth, and fifth cervical levels in 4 patients with Werdnig-Hoffmann disease revealed marked, generalized loss of motoneurons except for a cluster of large or medium-sized ones in the most medial portion of the anteromedial cell group. These well-preserved neurons were regarded as the phrenic motoneurons because diaphragmatic movement was the only muscle activity that remained until the last stage of illness. Furthermore, in its location and its cytoarchitectonic and neuronal characteristics, this neuronal cluster coincides with the phrenic nucleus as previously localized in the spinal cords of patients with phrenicotomy.

Entities:  

Mesh:

Year:  1981        PMID: 7271245     DOI: 10.1002/ana.410090515

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  2 in total

1.  Spontaneous Breathing Pattern as Respiratory Functional Outcome in Children with Spinal Muscular Atrophy (SMA).

Authors:  A LoMauro; A Aliverti; C Mastella; M T Arnoldi; P Banfi; G Baranello
Journal:  PLoS One       Date:  2016-11-07       Impact factor: 3.240

2.  A New Method for Measuring Bell-Shaped Chest Induced by Impaired Ribcage Muscles in Spinal Muscular Atrophy Children.

Authors:  Antonella LoMauro; Paolo Banfi; Chiara Mastella; Katia Alberti; Giovanni Baranello; Andrea Aliverti
Journal:  Front Neurol       Date:  2018-09-13       Impact factor: 4.003

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.