Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations-Reference-Cited by-同舟云学术

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Fatal Familial Insomnia: Clinical Aspects and Molecular Alterations

Published:2017-03-21 Issue:4 Volume:17 Page:
ISSN:1528-4042
Container-title:Current Neurology and Neuroscience Reports
language:en
Short-container-title:Curr Neurol Neurosci Rep

Author:

Llorens Franc,Zarranz Juan-José,Fischer Andre,Zerr Inga,Ferrer Isidro

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,General Neuroscience

Link

http://link.springer.com/content/pdf/10.1007/s11910-017-0743-0.pdf

Reference70 articles.

1. Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P, et al. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med. 1992;326:444–9.

2. Medori R, Montagna P, Tritschler HJ, LeBlanc A, Cortelli P, Tinuper P, Lugaresi E, Gambetti P. Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178. Neurology. 1992;42:669–70.

3. Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, et al. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science. 1992;258:806–8.

4. Zarranz JJ, Digon A, Atares B, Rodriguez-Martinez AB, Arce A, Carrera N, Fernandez-Manchola I, Fernandez-Martinez M, Fernandez-Maiztegui C, Forcadas I, Galdos L, Gomez-Esteban JC, Ibanez A, Lezcano E, Lopez de MA, Marti-Masso JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, de Pancorbo MM. Phenotypic variability in familial prion diseases due to the D178N mutation. J.Neurol.Neurosurg.Psychiatry. 2005;76:1491–6.

5. Johnson MD, Vnencak-Jones CL, McLean MJ. Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers. Neurology. 1998;51:1715–7.

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