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6. [A case of Creutzfeldt-Jakob disease with E200K mutation presenting with hearing loss and central hypoventilation]. Miyagawa S; Mukai T; Yaguchi H Rinsho Shinkeigaku; 2018 Nov; 58(11):673-676. PubMed ID: 30369525 [TBL] [Abstract][Full Text] [Related]
7. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Taratuto AL; Piccardo P; Reich EG; Chen SG; Sevlever G; Schultz M; Luzzi AA; Rugiero M; Abecasis G; Endelman M; Garcia AM; Capellari S; Xie Z; Lugaresi E; Gambetti P; Dlouhy SR; Ghetti B Neurology; 2002 Feb; 58(3):362-7. PubMed ID: 11839833 [TBL] [Abstract][Full Text] [Related]
8. Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD. Cohen OS; Chapman J; Korczyn AD; Nitsan Z; Appel S; Hoffmann C; Rosenmann H; Kahana E; Lee H J Neurol; 2015 Mar; 262(3):604-13. PubMed ID: 25522698 [TBL] [Abstract][Full Text] [Related]
11. Sleep Pathology in Creutzfeldt-Jakob Disease. Kang P; de Bruin GS; Wang LH; Ward BA; Ances BM; Lim MM; Bucelli RC J Clin Sleep Med; 2016 Jul; 12(7):1033-9. PubMed ID: 27250807 [TBL] [Abstract][Full Text] [Related]
12. Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families. Sarapura-Castro E; Cosentino C; Landman J; Landman A; Torres L; Nuñez Y; Capellari S; Parchi P; Cornejo-Olivas M Clin Neurol Neurosurg; 2021 Mar; 202():106490. PubMed ID: 33454496 [No Abstract] [Full Text] [Related]
13. [Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course]. Takayanagi M; Suzuki K; Nakamura T; Hirata K; Satoh K; Kitamoto T Rinsho Shinkeigaku; 2018 Nov; 58(11):682-687. PubMed ID: 30369528 [TBL] [Abstract][Full Text] [Related]
14. Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation. Chapman J; Arlazoroff A; Goldfarb LG; Cervenakova L; Neufeld MY; Werber E; Herbert M; Brown P; Gajdusek DC; Korczyn AD Neurology; 1996 Mar; 46(3):758-61. PubMed ID: 8618678 [TBL] [Abstract][Full Text] [Related]
15. Clinical manifestations and polysomnography-based analysis in nine cases of probable sporadic Creutzfeldt-Jakob disease. Dai Y; Shao J; Lang Y; Lv Y; Cui L Neurol Sci; 2021 Oct; 42(10):4209-4219. PubMed ID: 33559029 [TBL] [Abstract][Full Text] [Related]
16. CSF tau correlates with the degree of cortical involvement in E200K familial Creutzfeldt-Jakob disease. Cohen OS; Chapman J; Korczyn AD; Siaw OL; Warman-Alaluf N; Nitsan Z; Appel S; Kahana E; Rosenmann H; Hoffmann C Neurosci Lett; 2016 Nov; 634():76-78. PubMed ID: 27721036 [TBL] [Abstract][Full Text] [Related]
17. Precocious loss of physiological sleep in a case of Creutzfeldt Jakob disease: a serial polygraphic study. Terzano MG; Parrino L; Pietrini V; Mancia D; Spaggiari MC; Rossi G; Tagliavini F Sleep; 1995 Dec; 18(10):849-58. PubMed ID: 8746391 [TBL] [Abstract][Full Text] [Related]
18. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene. Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M Prion; 2014; 8(5):336-8. PubMed ID: 25495585 [TBL] [Abstract][Full Text] [Related]
19. Disease duration in E200K familial Creutzfeldt-Jakob disease is correlated with clinical, radiological, and laboratory variables. Cohen OS; Chapman J; Korczyn AD; Nitsan Z; Appel S; Kahana E; Rosenmann H; Hoffmann C J Neural Transm (Vienna); 2019 May; 126(5):607-611. PubMed ID: 30498951 [TBL] [Abstract][Full Text] [Related]
20. [Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case]. Cosacov RM; Taratuto AL; Ghiraridi G; Barrionuevo P; Diaz A; Begué C; Martinetto H Rev Fac Cien Med Univ Nac Cordoba; 2004; 61(1):48-53. PubMed ID: 15366237 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]