Clinical Features of Fatal Familial Insomnia: Phenotypic Variability in Relation to a Polymorphism at Codon 129 of the Prion Protein Gene-Reference-Cited by-同舟云学术

Clinical Features of Fatal Familial Insomnia: Phenotypic Variability in Relation to a Polymorphism at Codon 129 of the Prion Protein Gene

Published:2006-04-05 Issue:3 Volume:8 Page:515-520
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:

Author:

Montagna Pasquale,Cortelli Pietro,Avoni Patrizia,Tinuper Paolo,Plazzi Giuseppe,Gallassi Roberto,Portaluppi Francesco,Julien Jean,Vital Claude,Delisle Marie Bernadette,Gambetti Pierluigi,Lugaresi Elio

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.1998.tb00172.x/fullpdf

Reference15 articles.

1. Amino acid polymorphism in human prion protein and age at death in inherited prion disease;Baker;Lancet,1991

2. Allelic origin of the abnormal prion protein isoform in familial prion diseases;Chen;Nature Med,1997

3. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease;Collinge;Lancet,1991

4. Cardiovascular dysautonomia in fatal familial insomnia;Cortelli;Clin Autonom Res,1991

5. Cerebral metabolism in fatal familial insomnia: Relation to duration, neuropathology, and distribution of protease-resistent prion protein;Cortelli;Neurology,1997

Cited by 92 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. Agrypnia excitata: a human model to explore the derailment of sleep–wake cycle integrated control;Journal of Sleep Research;2024-09-02

2. The Role of PET Imaging in Patients with Prion Disease: A Literature Review;Molecular Imaging and Biology;2024-02-01

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

4. Can insomnia be fatal? An Australian case of fatal familial insomnia;Internal Medicine Journal;2022-04

5. Les maladies à prions ou encéphalopathies spongiformes transmissibles;La Revue de Médecine Interne;2022-02