These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 30369525)

  • 21. Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
    Szucs A; Várallyay P; Osztie E; Papp E; Sólyom A; Finta L; Varga D; Barcs G; Holló A; Kamondi A
    Ideggyogy Sz; 2012 Nov; 65(11-12):401-10. PubMed ID: 23289175
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Cheyne-Stokes respiration appeared in an early stage of the disease in a patient with Creutzfeldt-Jakob disease].
    Koh K; Nagasaka T; Kobayashi F; Yamashiro N; Shindo K; Takiyama Y
    Rinsho Shinkeigaku; 2013; 53(8):642-5. PubMed ID: 23965858
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. [Human prion diseases: the Hungarian experience].
    Kovács GG; Bakos A; Mitrova E; Minárovits J; László L; Majtényi K
    Ideggyogy Sz; 2007 Nov; 60(11-12):447-52. PubMed ID: 18200749
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Familial Creutzfeldt-Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course.
    Nitsan Z; Cohen OS; Chapman J; Kahana E; Korczyn AD; Appel S; Osherov M; Rosenmann H; Milo R
    J Neurol; 2020 Aug; 267(8):2455-2458. PubMed ID: 32367297
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction.
    Iwasaki Y; Mori K; Ito M; Akagi A; Mimuro M; Kitamoto T; Yoshida M
    Neuropathology; 2017 Dec; 37(6):575-581. PubMed ID: 28703419
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.
    Begué C; Martinetto H; Schultz M; Rojas E; Romero C; D'Giano C; Sevlever G; Somoza M; Taratuto AL
    Neuroepidemiology; 2011; 37(3-4):193-202. PubMed ID: 22067221
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [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]  

  • 31. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.
    Shi Q; Shen XJ; Zhou W; Xiao K; Zhang XM; Zhang BY; Dong XP
    Prion; 2014; 8(6):411-4. PubMed ID: 25482600
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A longitudinal
    Chu M; Chen Z; Nie B; Liu L; Xie K; Cui Y; Chen K; Rosa-Neto P; Wu L
    J Neurol; 2022 Nov; 269(11):6094-6103. PubMed ID: 35864212
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Rare genetic E196A mutation in a patient with Creutzfeldt-Jakob disease: a case report and literature.
    Wu X; Cui Z; Guomin X; Wang H; Zhang X; Li Z; Sun Q; Qi F
    Prion; 2020 Dec; 14(1):143-148. PubMed ID: 32501129
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease.
    Zhang H; Wang M; Wu L; Zhang H; Jin T; Wu J; Sun L
    J Clin Neurosci; 2014 Jan; 21(1):175-8. PubMed ID: 23787189
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Familial Creutzfeldt-Jakob Disease with a codon 200 mutation presenting as thalamic syndrome: diagnosis by single photon emission computed tomography using (99m)Tc-ethyl cysteinate dimer.
    Konno S; Murata M; Toda T; Yoshii Y; Nakazora H; Nomoto N; Sugimoto H; Nemoto H; Wakata N; Fujioka T; Kurihara T
    Intern Med; 2008; 47(1):65-7. PubMed ID: 18176009
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
    Mitrová E; Belay G
    Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry.
    Iwasaki Y; Mori K; Ito M; Kawai Y
    Prion; 2019 Jan; 13(1):151-155. PubMed ID: 31387445
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic Creutzfeldt-Jakob disease with an 8-year disease course.
    Renard D; Orgeval J; Sazdovitch V; Seilhean D; Thouvenot E
    Acta Neurol Belg; 2018 Jun; 118(2):313-314. PubMed ID: 29704165
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.