Conclusions of the Symposium

Author:

Gambetti Pierluigi,Lugaresi Elio

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Reference28 articles.

1. A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease;Bosque;Neurology,1992

2. Brown P Cervenakofa L Powers JM. Fatal familial insomnia in the United States, Australia, and Japan Brain Pathology , this issue

3. Budka H Aimer G Hainfellner JA Brucke T Jellinger K. FFI in Europe and around the world Brain Pathology , this issue

4. Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation;Chapman;J Neurol Neurosurg Psychiatry,1993

5. Dorandeu A Wingertsmann L Chretien F Delisle MB Vital C Parchi P Montagna M Lugaresi E Ironside J Budka H Gambetti P Gray F. Neuronal apoptosis in Fatal Familial Insomnia Brain Pathology , this issue

Cited by 12 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. Genetic Factors in Sleep Disorders: What Are the Roles of Genetic Factors in the Pathogenesis of Sleep Disorders?;Respiratory Disease Series: Diagnostic Tools and Disease Managements;2018

2. Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations;Current Neurology and Neuroscience Reports;2017-03-21

3. Sleep disorders;Human Fatigue Risk Management;2016

4. Creutzfeldt-Jakob Disease and Other Prion Disorders;Viral Encephalitis in Humans;2014-04-08

5. Sporadic fatal insomnia with clinical, laboratory, and genetic findings;Journal of Clinical Neuroscience;2012-08

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