๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Neuromuscular Disorders (Tawil/Neuromuscular Disorders) || Hereditary Motor Sensory Neuropathies (Charcot-Marie-Tooth Disease)

โœ Scribed by Tawil, Rabi N.; Venance, Shannon


Book ID
121866637
Publisher
Wiley-Blackwell
Year
2011
Weight
507 KB
Category
Article
ISBN
0470654562

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Vincristine neuropathy in type I and typ
โœ Igarashi, Masanori ;Thompson, Elizabeth I. ;Rivera, Gaston K. ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 827 KB

## Abstract A patient with Ewing's sarcoma and demyelinating type Charcotโ€Marieโ€Tooth disease (CMT) developed severe neuropathy after receiving a total vincristine dose of 6 mg. Recovery was slow and incomplete. A second patient with axonal type CMT developed moderate neuropathy but tolerated exten

Schwann cells and the pathogenesis of in
โœ Philipp Berger; Axel Niemann; Ueli Suter ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 361 KB

## Abstract Over the last 15 years, a number of mutations in a variety of genes have been identified that lead to inherited motor and sensory neuropathies (HMSN), also called Charcotโ€Marieโ€Tooth disease (CMT). In this review we will focus on the molecular and cellular mechanisms that cause the Schw

Duplication of part of chromosome 17 is
โœ P. J. Hallam; A. E. Harding; J. Berciano; D. F. Barker; Dr S. Malcolm ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 477 KB ๐Ÿ‘ 3 views

Hereditary motor and sensory neuropathy type I (HMSNI), also known as Charcot-Marie-Tooth disease type 1 (CMTl), has been shown to be genetically heterogeneous. A major gene maps to chromosome 17 (CMTlA). A set of loci, D17S122, D17S125, and D17S124, show tight linkage to the C M T l A locus, and a