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P. Vitali, E. Maccagnano, E. Caverzasi, R. G. Henry, A. Haman, C. Torres-Chae, D. Y. Johnson, B. L. Miller and M. D. Geschwind, “Diffusion-Weighted MRI Hyperintensity Patterns Differentiate CJD from Other Rapid Dementias,” Neurology, Vol. 76, No. 20, 2011, pp. 17111719. doi:10.1212/WNL.0b013e31821a4439

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.