Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases-Reference-Cited by-同舟云学术

Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases

Published:1986-11 Issue:5 Volume:20 Page:597-602
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Brown Paul,Cathala Fran�oise,Castaigne Paul,Gajdusek D. Carleton

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference38 articles.

1. Partial elementary motor seizures as the first symptom of Creutzfeldt-Jakob disease

2. Periodic lateralized epileptiform complexes (PLEDs) in Creutzfeldt-Jakob disease

3. et al: Early Clinical features of Creutzfeldt-Jakob disease (subacute spongiform encephalopathy). In (eds): Slow Transmissible Diseases of the Nervous System, Vol 1. New York, Academic, 1979, pp 229-251

4. Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease

5. Creutzfeldt–Jakob Disease Prion Proteins in Human Brains

Cited by 372 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. Supranuclear Vertical Gaze Palsy in Movement Disorders;Neuro-Ophthalmology;2024-07-17

2. Longitudinal microbiome investigation throughout prion disease course reveals pre- and symptomatic compositional perturbations linked to short-chain fatty acid metabolism and cognitive impairment in mice;Frontiers in Microbiology;2024-06-11

3. Paraneoplastic cerebellar and brainstem disorders;Handbook of Clinical Neurology;2024

4. Probable Sporadic Creutzfeldt-Jakob Disease Presenting as Refractory Status Epilepticus in a Poststroke Epilepsy Patient: A Case Report;NMC Case Report Journal;2023-12-31

5. Personalized brain MRI revealed distinct functional and anatomical disruptions in Creutzfeldt‐Jakob disease and Alzheimer's disease;CNS Neuroscience & Therapeutics;2023-08-14