The Three Glycotypes in the London Classification System of Sporadic Creutzfeldt-Jakob Disease Differ in Disease Duration-Reference-Cited by-同舟云学术

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The Three Glycotypes in the London Classification System of Sporadic Creutzfeldt-Jakob Disease Differ in Disease Duration

Published:2021-04-26 Issue:8 Volume:58 Page:3983-3991
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Ney Blair^ORCID,Eratne Dhamidhu^ORCID,Lewis Victoria^ORCID,Ney Luke^ORCID,Li Qiao-Xin^ORCID,Stehmann Christiane^ORCID,Collins Steven^ORCID,Velakoulis Dennis^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

https://link.springer.com/content/pdf/10.1007/s12035-021-02396-9.pdf

Reference47 articles.

1. Johnson RT (2005) Prion diseases. Lancet Neurol 4:635–642

2. Prusiner SB (1998) Prions. Proc Natl Acad Sci 95:13363–13383

3. Sparkes RS, Simon M, Cohn VH et al (1986) Assignment of the human and mouse prion protein genes to homologous chromosomes. Proc Natl Acad Sci 83:7358–7362

4. Zahn R, Liu A, Lührs T et al (2000) NMR solution structure of the human prion protein. Proc Natl Acad Sci 97:145–150

5. Knaus KJ, Morillas M, Swietnicki W et al (2001) Crystal structure of the human prion protein reveals a mechanism for oligomerization. Nat Struct Biol 8:770–774

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1. Assessing the newly proposed MRI criteria for diagnosing sporadic Creutzfeldt-Jakob disease;Neuroradiology;2024-08-13

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