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C. Gao, Q. Shi, C. Tian, C. Chen, J. Han, W. Zhou, B. Y. Zhang, H. Y. Jiang, J. Zhang and X. P. Dong, “The Epidemiological, Clinical, and Laboratory Features of Sporadic Creutzfeldt-Jakob Disease Patients in China: Surveillance Data from 2006 to 2010,” PLoS One, Vol. 6, No. 8, 2011, Article ID: e24231. doi:10.1371/journal.pone.0024231

has been cited by the following article:

• TITLE: Sporadic Creutzfeldt-Jakob Disease Presenting with Visual Disturbance—A Case Report in China

  AUTHORS: Guohong Tian, Lin Sun, Yunhong He, Xiaojun Zhang

  KEYWORDS: Creutzfeldt-Jakob Disease; Visual Disturbance; Heidenhain Variant; Diffusion Weighted Imaging

  JOURNAL NAME: International Journal of Clinical Medicine, Vol.4 No.7, July 4, 2013

  ABSTRACT: Creutzfeldt-Jakob disease (CJD) is a rare but fatal neurodegenerative prion disease. Classic CJD comprises a clinical triad of rapidly progressive dementia, myoclonus, and EEG abnormality. At initial presentation, this classic triad is present only in a minority of cases. Visual impairment is one of the predominant manifestations in the course of CJD, especially in Heidenhain variant phenotype. We reported a case presenting with progressive blurred vision, along with other neurological symptoms, who diagnosed as sporadic CJD with cortical blindness in China.