𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

✍ Scribed by A. Cruz-Martínez; S. Bort; J. Arpa; J. Duarte; F. Palau


Book ID
111063914
Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
898 KB
Volume
4
Category
Article
ISSN
1351-5101

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Recurrent brachial plexus palsies as the
✍ Florian Stögbauer; Peter Young; Max Kerschensteiner; E. Bernd Ringelstein; Gerd 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 72 KB 👁 2 views

There is phenotypic heterogeneity in patients with hereditary neuropathy with liability to pressure palsies. In rare cases, recurrent brachial plexopathy is the only expression of the disease. We describe a patient with three episodes of plexus brachialis palsy and a de novo deletion of the peripher