Fatal familial insomnia presenting with agrypnia excitata and very low atonia index level-Reference-Cited by-同舟云学术

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Fatal familial insomnia presenting with agrypnia excitata and very low atonia index level

Published:2018-05 Issue:18 Volume:97 Page:e0646
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Yang Tae-Won,Park Byeongsu,Kim Keun Tae,Jun Jin-Sun,Kim Young-Soo,Lee Soon-Tae,Jung Keun-Hwa,Chu Kon,Lee Sang Kun,Jung Ki-Young

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference10 articles.

1. Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene;Sun;Prion,2015

2. Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei;Lugaresi;N Engl J Med,1986

3. A proposal of new diagnostic pathway for fatal familial insomnia;Krasnianski;J Neurol Neurosurg Psychiatry,2014

4. Behavioral and polygraphic study of “sleep” and “wakefulness” in chronic decerebrate cats;Villablanca;Electroencephalogr Clin Neurophysiol,1966

5. Agrypnia excitata: clinical features and pathophysiological implications;Lugaresi;Sleep Med Rev,2001

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1. A systemic analysis of Creutzfeldt Jakob disease cases in Asia;Prion;2024-02-07

2. Sporadic Fatal Insomnia presenting with agrypnia excitata and rapidly progressive dementia: a case report;Journal of Neurology;2023-02-22

3. Prion Mutations in Republic of Republic of Korea, China, and Japan;International Journal of Molecular Sciences;2022-12-30

4. A case of rapidly progressive insomnia and dysautonomia;Annals of the Academy of Medicine, Singapore;2022-08-29

5. REM sleep behavior disorder: Mimics and variants;Sleep Medicine Reviews;2021-12

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