๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Symmetry of phrenic nerve motor response in amyotrophic lateral sclerosis

โœ Scribed by Susana Pinto; Mamede de Carvalho

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
417 KB
Volume
42
Category
Article
ISSN
0148-639X

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Motor responses of the sternocleidomasto
Motor responses of the sternocleidomastoid muscle in patients with amyotrophic lateral sclerosis
โœ Susana Pinto; Mamede de Carvalho ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 100 KB

## Abstract The sternocleidomastoid muscle (SCM) is an accessory inspiratory muscle, but it is not investigated systematically in patients with amyotrophic lateral sclerosis (ALS). We aimed to study the involvement of the SCM and to evaluate the role of the diaphragm and SCM on respiratory tests pe

Longitudinal tracking of the same single
Longitudinal tracking of the same single motor unit in amyotrophic lateral sclerosis
โœ Clifton L. Gooch; Yadollah Harati ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 169 KB ๐Ÿ‘ 2 views

The electrophysiologic study of motor units in the Houston Veteran's Affairs Medical Center. Informed consent was obtained from all subjects. human patient has a long history, 1,3,5,9,12 and the recent revival of interest in motor unit number estimation (MUNE) 2,4,6,10,11,13,14 has prompted the refi

Functional significance of upper and low
Functional significance of upper and lower motor neuron impairment in amyotrophic lateral sclerosis
โœ Jane A. Kent-Braun; Christie H. Walker; Michael W. Weiner; Robert G. Miller ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 132 KB ๐Ÿ‘ 2 views

The objective of this study was to examine the contribution of lower motor neuron (LMN) and upper motor neuron (UMN) dysfunction to weakness and impaired motor control in 27 patients with amyotrophic lateral sclerosis (ALS). Isometric strength was measured by dorsiflexor maximum voluntary contractio

Progressive motor neuron impairment in a
Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis
โœ Mimoun Azzouz; Nathalie Leclerc; Mark Gurney; Jean-Marie Warter; Philippe Poindr ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 114 KB ๐Ÿ‘ 2 views

Mutations of Cu,Zn superoxide dismutase cause an autosomal dominant form of familial amyotrophic lateral sclerosis. An animal model of the disease has been produced by expressing mutant human SOD1 in transgenic mice (G93A). In order to quantify the dysfunction of the motor unit in transgenic mice, e