Clinical and neuroimaging features of a Chinese patient with fatal familial insomnia
Author:
Funder
Medical Science and Technology Plan Projects of Henan Province
Publisher
Elsevier BV
Subject
General Medicine
Reference7 articles.
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2. Complex movement disorders in fatal familial insomnia: a clinical and genetic discussion;Pedroso;Neurology,2013
3. Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan;Nagayama;Neurology,1996
4. Serial positron emission tomographic findings in an atypical presentation of fatal familial insomnia;Bar;Arch Neurol,2002
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