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2. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2. Samman I; Schulz-Schaeffer WJ; Wöhrle JC; Sommer A; Kretzschmar HA; Hennerici M J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):678-81. PubMed ID: 10519881 [TBL] [Abstract][Full Text] [Related]
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4. Variant Creutzfeldt-Jakob disease in older patients. el Tawil S; Mackay G; Davidson L; Summers D; Knight R; Will R J Neurol Neurosurg Psychiatry; 2015 Nov; 86(11):1279-80. PubMed ID: 25609647 [No Abstract] [Full Text] [Related]
5. Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene. Furukawa F; Ishibashi S; Sanjo N; Yamashita H; Mizusawa H JAMA Neurol; 2014 Sep; 71(9):1186-7. PubMed ID: 25070174 [No Abstract] [Full Text] [Related]
6. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene. Tsuboi Y; Baba Y; Doh-ura K; Imamura A; Fujioka S; Yamada T J Neurol Sci; 2005 May; 232(1-2):45-9. PubMed ID: 15850581 [TBL] [Abstract][Full Text] [Related]
7. Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report. Kon T; Miki Y; Arai A; Funamizu Y; Ueno T; Haga R; Nishijima H; Suzuki C; Nunomura J; Baba M; Oyama Y; Shiga Y; Kitamoto T; Tomiyama M J Neurol Sci; 2015 May; 352(1-2):108-9. PubMed ID: 25818675 [No Abstract] [Full Text] [Related]
8. Diffusion tensor imaging in patients with Creutzfeldt-Jakob disease. Fujita K; Nakane S; Harada M; Izumi Y; Kaji R J Neurol Neurosurg Psychiatry; 2008 Nov; 79(11):1304-6. PubMed ID: 18940995 [No Abstract] [Full Text] [Related]
9. The diagnosis of human prion diseases. Kordek R Folia Neuropathol; 2000; 38(4):151-60. PubMed ID: 11693717 [TBL] [Abstract][Full Text] [Related]
10. [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180]. Tanaka T; Kinoshita I; Saitoh Y; Satoh K; Nishiura Y; Shirabe S; Kitamoto T No To Shinkei; 2004 Dec; 56(12):1025-8. PubMed ID: 15729879 [TBL] [Abstract][Full Text] [Related]
11. [A case of codon 232 mutation-induced Creutzfeldt-Jakob disease visualized by the MRI-FLAIR images with atypical clinical symptoms]. Saito T; Isozumi K; Komatsumoto S; Nara M; Suzuki K; Dohura K Rinsho Shinkeigaku; 2000 Jan; 40(1):51-4. PubMed ID: 10825802 [TBL] [Abstract][Full Text] [Related]
12. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Collins SJ; Sanchez-Juan P; Masters CL; Klug GM; van Duijn C; Poleggi A; Pocchiari M; Almonti S; Cuadrado-Corrales N; de Pedro-Cuesta J; Budka H; Gelpi E; Glatzel M; Tolnay M; Hewer E; Zerr I; Heinemann U; Kretszchmar HA; Jansen GH; Olsen E; Mitrova E; Alpérovitch A; Brandel JP; Mackenzie J; Murray K; Will RG Brain; 2006 Sep; 129(Pt 9):2278-87. PubMed ID: 16816392 [TBL] [Abstract][Full Text] [Related]
13. Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK. Bateman D; Hilton D; Love S; Zeidler M; Beck J; Collinge J Lancet; 1995 Oct; 346(8983):1155-6. PubMed ID: 7475612 [No Abstract] [Full Text] [Related]
15. Double mutations at codon 180 and codon 232 of the PRNP gene in an apparently sporadic case of Creutzfeldt-Jakob disease. Hitoshi S; Nagura H; Yamanouchi H; Kitamoto T J Neurol Sci; 1993 Dec; 120(2):208-12. PubMed ID: 8138811 [TBL] [Abstract][Full Text] [Related]
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17. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649 [TBL] [Abstract][Full Text] [Related]