Ørstavik, K <br/><br/>
Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies.  [electronic resource] 

 -  Muscle & nerve  Aug 2001 
 - 1093-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-639X 
<br/><br/><label>Standard No.: </label>10.1002/mus.1116  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brachial Plexus Neuropathies--complications<br/>Chromosomes, Human, Pair 17--genetics<br/>DNA Mutational Analysis<br/>Electrodiagnosis<br/>Electromyography<br/>Genes, Dominant<br/>Genetic Predisposition to Disease<br/>Humans<br/>Loss of Heterozygosity<br/>Male<br/>Median Nerve--physiopathology<br/>Middle Aged<br/>Myelin Proteins--deficiency<br/>Nerve Compression Syndromes--complications<br/>Neural Conduction<br/>Pedigree<br/>Peroneal Nerve--physiopathology