Electroencephalographic and polysomnographic findings in a patient with familial Creutzfeldt-Jakob disease-Reference-Cited by-同舟云学术

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Electroencephalographic and polysomnographic findings in a patient with familial Creutzfeldt-Jakob disease

Published:2018-11 Issue:9 Volume:33 Page:625-628
ISSN:2173-5808
Container-title:Neurología (English Edition)
language:en
Short-container-title:Neurología (English Edition)

Author:

Garnés Sánchez C.M.,López Bernabé R.,Miró-Andreu A.,Maeztu Sardiña M.C.,Salmerón-Ato P.

Publisher

Elsevier BV

Subject

General Materials Science

Reference11 articles.

1. Characterization of sleep disorders in patients with E200K familial Creutzfeldt-Jakob disease;Cohen;J Neurol,2015

2. Prion diseases;Knight;J Neurol Neurosurg Psychiatry,2004

3. Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin;Goldfarb;Lancet,1990

4. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease;Hsiao;N Engl J Med,1991

5. Creutzfeldt-Jakob disease surveillance in Argentina, 1997–2008;Begué;Neuroepidemiology,2011

Cited by 1 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. Misdiagnosis of rarest subtype of sporadic Creutzfeldt Jakob Disease: a case report;BMC Neurology;2023-07-18

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