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22. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis]. Imaiso Y; Mitsuo K Rinsho Shinkeigaku; 1998; 38(10-11):920-5. PubMed ID: 10203975 [TBL] [Abstract][Full Text] [Related]
23. PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia. Hall DA; Leehey MA; Filley CM; Steinbart E; Montine T; Schellenberg GD; Bosque P; Nixon R; Bird T Neurology; 2005 Apr; 64(7):1304-6. PubMed ID: 15824374 [TBL] [Abstract][Full Text] [Related]
24. Human prion diseases. Prusiner SB; Hsiao KK Ann Neurol; 1994 Apr; 35(4):385-95. PubMed ID: 8154865 [TBL] [Abstract][Full Text] [Related]
25. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome. Doh-ura K; Tateishi J; Kitamoto T; Sasaki H; Sakaki Y Ann Neurol; 1990 Feb; 27(2):121-6. PubMed ID: 2180366 [TBL] [Abstract][Full Text] [Related]
27. Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene. Laplanche JL; Hachimi KH; Durieux I; Thuillet P; Defebvre L; Delasnerie-Lauprêtre N; Peoc'h K; Foncin JF; Destée A Brain; 1999 Dec; 122 ( Pt 12)():2375-86. PubMed ID: 10581230 [TBL] [Abstract][Full Text] [Related]
28. [Prion dementias: nosology and diagnostic difficulties in the spectrum of Creutzfeld-Jakob encephalopathy]. Kálmán J; Járdánházy T; Cserháti A; Szekeres G; Demeter I; Berek I; Dobranovics I; Csernay L; Janka Z Orv Hetil; 1997 Mar; 138(12):731-7. PubMed ID: 9157343 [TBL] [Abstract][Full Text] [Related]
29. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family. Heldt N; Boellaard JW; Brown P; Cervenákova L; Doerr-Schott J; Thomas C; Scherer C; Rohmer F Clin Neuropathol; 1998; 17(4):229-34. PubMed ID: 9707339 [TBL] [Abstract][Full Text] [Related]
30. Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy. Brown P; Kenney K; Little B; Ironside J; Will R; Cervenáková L; Bjork RJ; San Martin RA; Safar J; Roos R Ann Neurol; 1995 Aug; 38(2):245-53. PubMed ID: 7654073 [TBL] [Abstract][Full Text] [Related]
32. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part I]. Zaborowski A Psychiatr Pol; 2004; 38(2):283-96. PubMed ID: 15307293 [TBL] [Abstract][Full Text] [Related]
33. [Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129]. Terao Y; Hitoshi S; Shimizu J; Sakuta M; Kitamoto T Rinsho Shinkeigaku; 1992 Aug; 32(8):880-3. PubMed ID: 1490317 [TBL] [Abstract][Full Text] [Related]
34. Early age of onset in fatal familial insomnia. Two novel cases and review of the literature. Harder A; Gregor A; Wirth T; Kreuz F; Schulz-Schaeffer WJ; Windl O; Plotkin M; Amthauer H; Neukirch K; Kretzschmar HA; Kuhlmann T; Braas R; Hahne HH; Jendroska K J Neurol; 2004 Jun; 251(6):715-24. PubMed ID: 15311348 [TBL] [Abstract][Full Text] [Related]
35. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. Jansen C; Parchi P; Capellari S; Strammiello R; Dopper EG; van Swieten JC; Kamphorst W; Rozemuller AJ J Neuropathol Exp Neurol; 2011 Aug; 70(8):698-702. PubMed ID: 21760536 [TBL] [Abstract][Full Text] [Related]
36. The prion diseases. Brown K; Mastrianni JA J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044 [TBL] [Abstract][Full Text] [Related]