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285 Peripheral neuropathy as the predominant manifestation of a mitochondrial DNA deletion

✍ Scribed by C. Lacroix; A. Rôtig; J. Boulloche; B. Parfait; P. Rustin; M. Brivet; A. Münnich; P. Landrieu


Book ID
114361186
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
147 KB
Volume
3
Category
Article
ISSN
1090-3798

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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