يعرض 1 - 10 نتائج من 227 نتيجة بحث عن '"E200K"', وقت الاستعلام: 1.64s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Sensory disturbances in Creutzfeldt-Jakob disease

    المؤلفون: Appel, ShmuelAff1, Aff2, IDs10072023070930_cor1, Cohen, Yael, Appel, Shira, Cohen, Oren S.Aff3, Aff4, Chapman, JoabAff3, Aff5, Rosenmann, Hanna, Nitsan, ZeevAff1, Aff2, Kahana, EstherAff1, Aff2

    المصدر: Neurological Sciences. 45(3):1057-1062

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  2. 2
    دورية أكاديمية
    The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

    المؤلفون: Bregman, NoaAff1, Aff2, Aff3, IDs12883023031938_cor1, Shiner, TamaraAff1, Aff2, Aff3, Kavé, GititAff1, Aff4, Alcalay, Roy, Gana-Weisz, Mali, Goldstein, Orly, Glinka, Tal, Aizenstein, OrnaAff6, Aff7, Bashat, Dafna BenAff3, Aff6, Alcalay, YifatAff2, Aff8, Mirelman, AnatAff2, Aff3, Aff9, Thaler, AvnerAff2, Aff3, Aff9, Giladi, NirAff2, Aff3, Aff10, Omer, NuritAff1, Aff2, Aff9

    المصدر: BMC Neurology. 23(1)

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  3. 3
    دورية أكاديمية
    Creutzfeldt–Jakob Disease Associated with E200K Mutation and SARS-CoV-2 Infection: Pure Coincidence or Neurodegenerative Acceleration?

    المؤلفون: Elisa Colaizzo, Luca Prosperini, Antonio Petrucci, Alessia Perna

    المصدر: Clinical and Translational Neuroscience, Vol 8, Iss 2, p 16 (2024)

    مصطلحات موضوعية: genetic CJD, mutation E200K, COVID-19, prion, neurodegeneration, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/2514-183X/8/2/16; https://doaj.org/toc/2514-183X

    URL الوصول: https://doaj.org/article/20196922f71b41a1905c9c2b21facb27

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  4. 4
    دورية أكاديمية
    The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol

    المؤلفون: Noa Bregman, Tamara Shiner, Gitit Kavé, Roy Alcalay, Mali Gana-Weisz, Orly Goldstein, Tal Glinka, Orna Aizenstein, Dafna Ben Bashat, Yifat Alcalay, Anat Mirelman, Avner Thaler, Nir Giladi, Nurit Omer

    المصدر: BMC Neurology, Vol 23, Iss 1, Pp 1-11 (2023)

    مصطلحات موضوعية: Creutzfeldt-Jakob Disease, Genetic Creutzfeldt-Jakob Disease, Prion disease, Prodromal CJD, Biomarkers, E200K, Neurology. Diseases of the nervous system, RC346-429

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1471-2377

    URL الوصول: https://doaj.org/article/ba96f32651c941c3803b22eb71035d6d

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  5. 5
    دورية أكاديمية
    Epidemiological and clinical characteristics of patients with late-onset Creutzfeldt-Jakob disease

    المؤلفون: Trachtenbroit, Iliya, Cohen, Oren S.Aff2, Aff3, Chapman, JoabAff3, Aff4, Rosenmann, Hanna, Nitsan, ZeevAff1, Aff6, Kahana, EstherAff1, Aff6, Appel, ShmuelAff1, Aff6, IDs10072022059299_cor7

    المصدر: Neurological Sciences. 43(7):4275-4279

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  6. 6
    دورية أكاديمية
    Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt–Jakob Disease (CJD)

    المؤلفون: Sae-Young Won, Yong-Chan Kim, Byung-Hoon Jeong

    المصدر: International Journal of Molecular Sciences, Vol 24, Iss 19, p 14831 (2023)

    مصطلحات موضوعية: prion, sporadic CJD, somatic mutation, pyrosequencing, E200K, V203I, Biology (General), QH301-705.5, Chemistry, QD1-999

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/1422-0067/24/19/14831; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

    URL الوصول: https://doaj.org/article/e2432d7763044d9cadc3db7770af5aae

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  7. 7
    دورية أكاديمية
    Homodimeric complexes of the 90–231 human prion: a multilayered computational study based on FMO/GRID-DRY approach

    المؤلفون: Paciotti, RobertoAff1, IDs00894022052442_cor1, Storchi, LorianoAff1, Aff2, Marrone, Alessandro

    المصدر: Journal of Molecular Modeling: Computational Chemistry - Life Science - Advanced Materials - New Methods. 28(8)

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  8. 8
    دورية أكاديمية
    Thalamic-insomnia phenotype in E200K Creutzfeldt–Jakob disease: A PET/MRI study

    المؤلفون: Hong Ye, Min Chu, Zhongyun Chen, Kexin Xie, Li Liu, Haitian Nan, Yue Cui, Jing Zhang, Lin Wang, Junjie Li, Liyong Wu

    المصدر: NeuroImage: Clinical, Vol 35, Iss , Pp 103086- (2022)

    مصطلحات موضوعية: Creutzfeldt–Jakob disease, Thalamus, Insomnia, PRNP gene, E200K, PET/MRI, Computer applications to medicine. Medical informatics, R858-859.7, Neurology. Diseases of the nervous system, RC346-429

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S2213158222001516; https://doaj.org/toc/2213-1582

    URL الوصول: https://doaj.org/article/d07689d704d64d7fb4b55511cc7de3a5

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  9. 9
    دورية أكاديمية
    Familial Creutzfeldt–Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course

    المؤلفون: Nitsan, ZeevAff1, Aff2, Cohen, Oren S.Aff3, Aff5, Chapman, JoabAff4, Aff5, Kahana, EstherAff1, Aff2, Korczyn, Amos D., Appel, ShmuelAff1, Aff2, Osherov, MichaelAff1, Aff2, Rosenmann, Hanna, Milo, RonAff1, Aff2

    المصدر: Journal of Neurology. 267(8):2455-2458

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  10. 10
    دورية أكاديمية
    CREUTZFELDT-JAKOB SYNDROME OF GENETIC ORIGIN: SERIES OF CASES IN THE ARGENTINIAN PATAGONIA

    المؤلفون: Exeni Díaz G., Costa M., Salman J., Ávila S.

    المصدر: BAG. Journal of Basic and Applied Genetics, Vol 31, Iss 1, Pp 7-13 (2020)

    مصطلحات موضوعية: familial creutzfeldt-jakob syndrome, prnp gene, e200k, cjd in patagonia, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: https://sag.org.ar/jbag/wp-content/uploads/2020/05/BAG_VXXXI_1_2020_ART1_WEB.pdf; https://doaj.org/toc/1852-6233

    URL الوصول: https://doaj.org/article/cfc9188dd6af410a8e6bdf60e5be378f

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