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Journal Abstract Search

96 related items for PubMed ID: 10637858

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  • 25. Fatal familial insomnia: sleep, neuroendocrine and vegetative alterations.
    Montagna P, Cortelli P, Gambetti P, Lugaresi E.
    Adv Neuroimmunol; 1995; 5(1):13-21. PubMed ID: 7795890
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  • 26. Circadian hormonal rhythms in two new cases of fatal familial insomnia.
    Avoni P, Cortelli P, Montagna P, Tinuper P, Sforza E, Contin M, Parchi P, Pierangeli G, Maltoni P, Pavani A.
    Acta Neurol (Napoli); 1991 Dec; 13(6):574-6. PubMed ID: 1805556
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  • 27. Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation.
    Sforza E, Montagna P, Tinuper P, Cortelli P, Avoni P, Ferrillo F, Petersen R, Gambetti P, Lugaresi E.
    Electroencephalogr Clin Neurophysiol; 1995 Jun; 94(6):398-405. PubMed ID: 7607093
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  • 28. In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.
    Haïk S, Galanaud D, Linguraru MG, Peoc'h K, Privat N, Faucheux BA, Ayache N, Hauw JJ, Dormont D, Brandel JP.
    Arch Neurol; 2008 Apr; 65(4):545-9. PubMed ID: 18413481
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  • 29. Dissociation in circadian rhythms in a pseudohypersomnia form of fatal familial insomnia.
    Dauvilliers Y, Cervena K, Carlander B, Espa F, Bassetti C, Claustrat B, Laplanche JL, Billiard M, Touchon J.
    Neurology; 2004 Dec 28; 63(12):2416-8. PubMed ID: 15623717
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  • 30. [Fatal familial insomnia].
    Delisle MB, Uro-Coste E, Gray F, Vital C.
    Clin Exp Pathol; 1999 Dec 28; 47(3-4):176-80. PubMed ID: 10472737
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  • 34. Can insomnia be fatal? An Australian case of fatal familial insomnia.
    Habteslassie D, McMahon M, Wimaleswaran H.
    Intern Med J; 2022 Apr 28; 52(4):667-670. PubMed ID: 35419959
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  • 35. Fatal familial insomnia with an unusual prion protein deposition pattern: an autopsy report with an experimental transmission study.
    Sasaki K, Doh-ura K, Wakisaka Y, Tomoda H, Iwaki T.
    Neuropathol Appl Neurobiol; 2005 Feb 28; 31(1):80-7. PubMed ID: 15634234
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  • 36. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].
    Iwaski Y, Sone M, Kato T, Yoshida E, Indo T, Yoshida M, Hashizume Y, Yamada M.
    Rinsho Shinkeigaku; 1999 Aug 28; 39(8):800-6. PubMed ID: 10586622
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  • 37. Fatal familial insomnia: a new Austrian family.
    Almer G, Hainfellner JA, Brücke T, Jellinger K, Kleinert R, Bayer G, Windl O, Kretzschmar HA, Hill A, Sidle K, Collinge J, Budka H.
    Brain; 1999 Jan 28; 122 ( Pt 1)():5-16. PubMed ID: 10050890
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  • 38. Genetic prion disease-associated myelodysplasia and SIADH in siblings.
    Chang FC, Berman Y, Buckland ME, MacKinlay N, McGlade A, Collins S, Ng K.
    Eur J Neurol; 2011 Dec 28; 18(12):e149-50. PubMed ID: 22097952
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  • 39. A case with a 120 base pair insertional mutation in the prion protein gene: the first case in Japan.
    Beck G, Kawano T, Naba I, Nishimura T, Sawada J, Hazama T.
    J Neurol Neurosurg Psychiatry; 2005 May 28; 76(5):756-7. PubMed ID: 15834045
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  • 40. Neuroimaging of NREM sleep in primary insomnia: a Tc-99-HMPAO single photon emission computed tomography study.
    Smith MT, Perlis ML, Chengazi VU, Pennington J, Soeffing J, Ryan JM, Giles DE.
    Sleep; 2002 May 01; 25(3):325-35. PubMed ID: 12003163
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