Author:
Lu Tingting,Pan Yuhang,Peng Lisheng,Qin Feng,Sun Xiaobo,Lu Zhengqi,Qiu Wei
Funder
team project of natural science foundation of Guangdong Province
national natural science foundation of China
science and technology planning project of Guangdong Province
science and technology planning project of Guangdon Province
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine
Reference22 articles.
1. Montagna P, Gambetti P, Cortelli P, Lugaresi E. Familial and sporadic fatal insomnia. Lancet Neurol. 2003;2(3):167–76.
2. Lugaresi E, Medori R, Montagna P, Baruzzi A, Cortelli P, Lugaresi A, et al. Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei. N Engl J Med. 1986;315(16):997–1003.
3. Chen S, Guan M, Shang JK, He S, Zhang ML, Ma MM, et al. Reduced cerebral blood flow in genetic prion disease with PRNP D178N-129M mutation: an arterial spin labeling MRI study. J Clin Neurosci. 2015;22(1):204–6.
4. Oberstein SA, Ferrari MD, Bakker E, van Gestel J, Kneppers AL, Frants RR, et al. Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research Group Neurology. 1999;52(9):1913–5.
5. Montagna P. Fatal familial insomnia: a model disease in sleep physiopathology. Sleep Med Rev. 2005;9(5):339–53.
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