Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Reference6 articles.
1. Johnson RT (2005) Prion diseases. Lancet Neurol 4:635–642
2. Baiardi S, Capellari S, Ladogana A, Strumia S, Santangelo M, Pocchiari M, Parchi P (2016) Revisiting the Heidenhain variant of Creutzfeldt-Jakob disease: evidence for prion type variability influencing clinical course and laboratory findings. J Alzheimers Dis 50(2):465–476
3. Cooper SA, Murray KL, Heath CA, Will RG, Knight RS (2005) Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant". Br J Ophthalmol 89(10):1341–1342
4. Imbriani P, Imbriani P, Marfia GA, Marciani MG, Poleggi A, Pocchiari M, Puoti G, Caltagirone C, Pisani A (2016) Heidenhain variant in two patients with inherited V210I Creutzfeldt-Jakob disease. Int J Neurosci 126(4):381–383
5. Amano Y, Kimura N, Hanaoka T, Aso Y, Hirano T, Murai H, Satoh K, Matsubara E (2015) Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging. Prion 9:29–33
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献