๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Astrocytes in amyotrophic lateral sclerosis: direct effects on motor neuron survival

โœ Scribed by K. A. Staats; L. Van Den Bosch


Publisher
Springer Netherlands
Year
2009
Tongue
English
Weight
525 KB
Volume
35
Category
Article
ISSN
0092-0606

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Astrocytes interact intimately with dege
โœ John B. Levine; Jiming Kong; Mark Nadler; Zuoshang Xu ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 879 KB

Astrocytic proliferation and hypertrophy (astrogliosis) are associated with neuronal injury. However, neither the temporal nor the spatial relationship between astrocytes and injured neurons is clear, especially in neurodegenerative diseases. We investigated these questions in a mouse amyotrophic la

Electrodiagnostic studies in amyotrophic
โœ Jasper R. Daube ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 244 KB ๐Ÿ‘ 2 views

The clinical electrodiagnostic medicine (EDX) consultant asked to assess patients with suspected amyotrophic lateral sclerosis (ALS) has a number of responsibilities. Among the most important is to provide a clinical assessment in conjunction with the EDX study. The seriousness of the diagnoses and

Microglia as potential contributors to m
โœ Siranush A. Sargsyan; Peter N. Monk; Pamela J. Shaw ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 157 KB

## Abstract The central nervous system (CNS) is equipped with a variety of cell types, all of which are assigned particular roles during the development, maintenance, function and repair of neural tissue. One glial cell type, microglia, deserves particular attention, as its role in the healthy or i

Functional significance of upper and low
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