Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene-Reference-Cited by-同舟云学术

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Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene

Published:2000-04-25 Issue:8 Volume:54 Page:1641-1646
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Hauw J.-J.,Sazdovitch V.,Laplanche J.-L.,Peoc'h K.,Kopp N.,Kemeny J.,Privat N.,Delasnerie-Laupretre N.,Brandel J. P.,Deslys J. P.,Dormont D.,Alperovitch A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 58 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

1. The definition of precision medicine in neurodegenerative disorders and the one disease-many diseases tension;Precision Medicine in Neurodegenerative Disorders, Part I;2023

2. Amino Acid Substitution within Seven-Octapeptide Repeat Insertions in the Prion Protein Gene Associated with Short-Term Course;Viruses;2022-10-13

3. A clinicopathological study of selected cognitive impairment cases in Lothian, Scotland: enhanced CJD surveillance in the 65 + population group;BMC Geriatrics;2022-07-20

4. The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy;Neurological Sciences;2022-01-28

5. Accuracy of diagnosis criteria in patients with suspected diagnosis of sporadic Creutzfeldt-Jakob disease and detection of 14-3-3 protein, France, 1992 to 2009;Eurosurveillance;2017-10-12

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