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2. One genetic mutation, two diseases: fatal familial insomnia and Creutzfeldt-Jakob disease. Bellows JG Compr Ther; 1993; 19(1):3. PubMed ID: 8334858 [No Abstract] [Full Text] [Related]
3. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity. Gelpi E; Kovacs GG; Ströbel T; Koperek O; Voigtländer T; Liberski PP; Budka H Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763 [TBL] [Abstract][Full Text] [Related]
4. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction]. Peoc'h K Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969 [TBL] [Abstract][Full Text] [Related]
5. Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation. Shiraishi A; Mizusawa H; Yamada M J Neurol; 2002 Dec; 249(12):1740-1. PubMed ID: 12529802 [No Abstract] [Full Text] [Related]
6. Human prion diseases. Prusiner SB; Hsiao KK Ann Neurol; 1994 Apr; 35(4):385-95. PubMed ID: 8154865 [TBL] [Abstract][Full Text] [Related]
8. [Prions]. Scheffer U Med Klin (Munich); 1995 Nov; 90(11):653-7. PubMed ID: 8569634 [No Abstract] [Full Text] [Related]
9. Prion disease. Eggenberger E Neurol Clin; 2007 Aug; 25(3):833-42, viii. PubMed ID: 17659192 [TBL] [Abstract][Full Text] [Related]
10. Mutations and polymorphisms in the prion protein gene. Palmer MS; Collinge J Hum Mutat; 1993; 2(3):168-73. PubMed ID: 8364585 [TBL] [Abstract][Full Text] [Related]
11. [Prion protein coden 129 polymorphism (Val/Met) in a case of sporadic progressive multisystem degenerative disease]. Komai K; Masaharu T; Kitamoto T Rinsho Shinkeigaku; 1993 Jun; 33(6):666-7. PubMed ID: 8403690 [No Abstract] [Full Text] [Related]
12. Prions: protein aggregation and infectious diseases. Aguzzi A; Calella AM Physiol Rev; 2009 Oct; 89(4):1105-52. PubMed ID: 19789378 [TBL] [Abstract][Full Text] [Related]
13. Understanding the natural variability of prion diseases. Geissen M; Krasemann S; Matschke J; Glatzel M Vaccine; 2007 Jul; 25(30):5631-6. PubMed ID: 17391814 [TBL] [Abstract][Full Text] [Related]
14. [Prions and the problems they raise]. Burny A Bull Mem Acad R Med Belg; 1997; 152(6):247-63. PubMed ID: 9581369 [TBL] [Abstract][Full Text] [Related]
15. [Transmissible spongiform encephalopathies (prion diseases)--molecular principles and in vitro models]. Kretzschmar H Wien Med Wochenschr; 1998; 148(4):67-73. PubMed ID: 9611345 [TBL] [Abstract][Full Text] [Related]
16. Assessing the signatures of selection in PRNP from polymorphism data: results support Kreitman and Di Rienzo's opinion. Soldevila M; Calafell F; Helgason A; Stefánsson K; Bertranpetit J Trends Genet; 2005 Jul; 21(7):389-91. PubMed ID: 15913833 [No Abstract] [Full Text] [Related]
17. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129]. Colombier C; Géraud G; Delisle MB; Laplanche JL; Pavy le Traon A; Alizé P; Delpla PA Rev Neurol (Paris); 1997 May; 153(4):239-43. PubMed ID: 9296141 [TBL] [Abstract][Full Text] [Related]
18. Polymorphism at residue 129 modulates the conformational conversion of the D178N variant of human prion protein 90-231. Apetri AC; Vanik DL; Surewicz WK Biochemistry; 2005 Dec; 44(48):15880-8. PubMed ID: 16313190 [TBL] [Abstract][Full Text] [Related]