๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

C Histomorphology of neuromuscular junction in Duchenne muscular dystrophy

โœ Scribed by MARY C THEROUX; ALICIA OLIVANT; ROBERT E AKINS

Book ID
109030420
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
125 KB
Volume
18
Category
Article
ISSN
1155-5645

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Duchenne muscular dystrophy and the neur
Duchenne muscular dystrophy and the neuromuscular junction: The utrophin link
โœ Anthony O. Gramolini; Bernard J. Jasmin ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 875 KB

## Abstract Although the precise function of utrophin at the postsynaptic membrane of the neuromuscular junction still remains unclear, despite recent genetic โ€˜knockoutโ€™ experiments^(1,2)^, a separate study in a transgenic mouse model system for Duchenne muscular dystrophy (DMD) has nonetheless sho

Lung function in Duchenne muscular dystr
Lung function in Duchenne muscular dystrophy
โœ C. S. B. Galasko; J. B. Williamson; C. M. Delaney ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Springer ๐ŸŒ English โš– 586 KB

Over 90% of patients with Duchenne muscular dystrophy develop a scoliosis when they become wheelchair bound. The scoliosis is progressive and is associated with deteriorating lung function. The purpose of this study was firstly to assess whether a standing regimen, in patients who had gone off their