๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis

โœ Scribed by Richard W. Orell; James Habgood; Petter Rudge; Russell J. M. Lane; Jackie S. de Belleroche

Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
313 KB
Volume
39
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.

โœฆ Synopsis

The site, structure and frequency of intracranial aneurysms, angiomas and arteriovenous abnormalities. In: Millikan CH, ed. Research publications, association for research in nervous and mental disease. Baltimore:

๐Ÿ“œ SIMILAR VOLUMES

TDP-43 mutation in familial amyotrophic
TDP-43 mutation in familial amyotrophic lateral sclerosis
โœ Akio Yokoseki; Atsushi Shiga; Chun-Feng Tan; Asako Tagawa; Hiroyuki Kaneko; Akih ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 388 KB ๐Ÿ‘ 2 views
Corticomotor threshold is reduced in ear
Corticomotor threshold is reduced in early sporadic amyotrophic lateral sclerosis
โœ Kerry R. Mills; Kannan A. Nithi ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 58 KB ๐Ÿ‘ 1 views

The pathogenesis of idiopathic amyotrophic lateral sclerosis (ALS) remains unknown, but accumulating evidence suggests a neuroexcitotoxic mechanism may have some credence. Glutamate-induced hyperexcitability of cortical or spinal motoneurons may be expected to manifest itself as a reduced threshold

Outcomes research in amyotrophic lateral
Outcomes research in amyotrophic lateral sclerosis: Lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database
โœ Robert G. Miller; Fred Anderson; Benjamin Rix Brooks; Hiroshi Mitsumoto; Walter ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 62 KB ๐Ÿ‘ 1 views

Objective: To examine the care of patients with ALS following the publication of the standardized recommendations for the management of patients with amyotrophic lateral sclerosis (ALS) published in 1999 by the American Academy of Neurology. Methods: Specific aspects of ALS patient management have b