✦ LIBER ✦

Lymphoma, motor neuron diseases, and amyotrophic lateral sclerosis

✍ Scribed by Dr D. S. Younger; L. P. Rowland; N. Latov; A. P. Hays; D. J. Lange; W. Sherman; G. Inghirami; M. A. Pesce; D. M. Knowles; J. Powers; J. R. Miller; M. R. Fetell; R. E. Lovelace

Publisher: John Wiley and Sons
Year: 1991
Tongue: English
Weight: 843 KB
Volume: 29
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.410290114

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Electrodiagnostic studies in amyotrophic

Electrodiagnostic studies in amyotrophic lateral sclerosis and other motor neuron disorders

✍ Jasper R. Daube 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 244 KB 👁 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

What's in a name? Amyotrophic lateral sc

What's in a name? Amyotrophic lateral sclerosis, motor neuron disease, and allelic heterogeneity

✍ Lewis P. Rowland 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 387 KB 👁 1 views

The motor cortex and amyotrophic lateral

The motor cortex and amyotrophic lateral sclerosis

✍ Andrew Eisen; Markus Weber 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 167 KB

## Abstract On theoretical grounds, abnormalities of the motor cortex in patients with amyotrophic lateral sclerosis (ALS) could lead to anterograde (“dying‐forward”) transneuronal degeneration of the anterior horn cells as suggested by Charcot. Conversely, retrograde (“dying‐back”) degeneration of

Functional significance of upper and low

Functional significance of upper and lower motor neuron impairment in amyotrophic lateral sclerosis

✍ Jane A. Kent-Braun; Christie H. Walker; Michael W. Weiner; Robert G. Miller 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 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

Microglia as potential contributors to m

Microglia as potential contributors to motor neuron injury in amyotrophic lateral sclerosis

✍ Siranush A. Sargsyan; Peter N. Monk; Pamela J. Shaw 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 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

Progressive motor neuron impairment in a

Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

✍ Mimoun Azzouz; Nathalie Leclerc; Mark Gurney; Jean-Marie Warter; Philippe Poindr 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 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