المؤلفون: Nafe Reinhold, Arendt Christophe T., Hattingen Elke

المصدر: Translational Neuroscience, Vol 14, Iss 1, Pp 60-83 (2023)

مصطلحات موضوعية: creutzfeldt–jakob disease, variably protease-sensitive prionopathy, fatal familial insomnia, gerstmann–sträussler–scheinker disease, kuru, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2081-6936Test

الوصول الحر: https://doaj.org/article/4b467cf5c7a54ea283fbe27c0387d6efTest

المؤلفون: Habteslassie, Daniel¹ dhabteslassie@gmail.com, McMahon, Marcus^1,2, Wimaleswaran, Hari^1,2,3

المصدر: Internal Medicine Journal. Apr2022, Vol. 52 Issue 4, p667-670. 4p.

مصطلحات موضوعية: *FATAL familial insomnia, *PRION diseases, *MOTOR neuron diseases, *POLYSOMNOGRAPHY, *GENETIC testing, *SLEEP, *DYSAUTONOMIA, *SYMPTOMS

العنوان البديل: Agrypnia Excitata: A Case of Delirium Tremens and Review of the Literature.

المؤلفون: Kavla, Yasin¹ yasinkavla@gmail.com, Gezer, Tuğrul^1,2, Şenel, Gülçin Benbir^1,2

المصدر: Journal of Turkish Sleep Medicine. Sep2021, Vol. 8 Issue 3, p174-179. 6p.

مصطلحات موضوعية: *FATAL familial insomnia, *ENCEPHALITIS, *DIPLOPIA, *HALLUCINATIONS, *NEUROLOGICAL disorders, *ALCOHOL withdrawal delirium, *AUTOIMMUNE diseases, *INSOMNIA

المؤلفون: Soldevila Trepat, Marta

المساهمون: University/Department: Universitat Pompeu Fabra. Departament de Ciències Experimentals i de la Salut

مرشدي الرسالة: Bertranpetit, Jaume

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: primats, ximpanzé, Creutzfeldt-Jakob, Insomni Fatal familiar, BSE, malalties priòniques, selecció balancejadora, selecció positiva, selecció, seqüència, haplotip, canibalisme, CJD, prió, PRNP, primates, chimpanzee, Fatal familial insomnia, prion diseases, balancing selection, positive selection, selection, sequence, haplotypes, cannibalism, prion

وصف الملف: application/pdf

الوصول الحر: http://www.tdx.cat/TDX-0202110-115800Test
http://hdl.handle.net/10803/7189Test

المؤلفون: Katrin Thüne, Matthias Schmitz, John Wiedenhöft, Orr Shomroni, Stefan Göbel, Timothy Bunck, Neelam Younas, Saima Zafar, Peter Hermann, Inga Zerr

المصدر: Cells, Vol 12, Iss 16, p 2053 (2023)

مصطلحات موضوعية: fatal familial insomnia, genetic variants, age of onset, whole-exome sequencing, Cytology, QH573-671

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2073-4409/12/16/2053Test; https://doaj.org/toc/2073-4409Test

الوصول الحر: https://doaj.org/article/eeca6d89cbe34221a46967e221f5714cTest

المؤلفون: Thüne, Katrin, Schmitz, Matthias, Wiedenhöft, John, Shomroni, Orr, Göbel, Stefan, Bunck, Timothy, Younas, Neelam, Zafar, Saima, Hermann, Peter, Zerr, Inga

المصدر: Cells 12(16), 2053 (2023). doi:10.3390/cells12162053 special issue: "Pathogenesis of Prion Diseases"

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Humans, Insomnia, Fatal Familial: genetics, Exome Sequencing, Age of Onset, Genes, Regulator, Prions, Prion Proteins: genetics, fatal familial insomnia, genetic variants, whole-exome sequencing, Prion Proteins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:37626863; info:eu-repo/semantics/altIdentifier/issn/2073-4409; https://pub.dzne.de/record/263613Test; https://pub.dzne.de/search?p=id:%22DZNE-2023-00835%22Test

الإتاحة: https://doi.org/10.3390/cells12162053Test
https://pub.dzne.de/record/263613Test
https://pub.dzne.de/search?p=id:%22DZNE-2023-00835%22Test

المؤلفون: Barbara Madoń, Eryk Mikos, Justyna Nowaczek, Martyna Wasyluk, Natalia Wilczek

المصدر: Journal of Education, Health and Sport, Vol 11, Iss 9, Pp 29-36 (2021)

مصطلحات موضوعية: prion diseases, fatal familial insomnia, neurodegeneration, ffi treatment, prion, Education, Sports, GV557-1198.995, Medicine

وصف الملف: electronic resource

العلاقة: https://apcz.umk.pl/czasopisma/index.php/JEHS/article/view/35109Test; https://doaj.org/toc/2391-8306Test

الوصول الحر: https://doaj.org/article/1bd284c0e0924399929734c9cdfbde4fTest

المؤلفون: Brian S. Appleby, Shashirekha Shetty, Mohamed Elkasaby

المصدر: Frontiers in Neurology, Vol 13 (2022)

مصطلحات موضوعية: prion disease, Creutzfeldt-Jakob disease, Gerstmann-Sträussler Scheinker disease, fatal familial insomnia, genetic Creutzfeldt–Jakob disease, genetics, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2022.1003056/fullTest; https://doaj.org/toc/1664-2295Test

الوصول الحر: https://doaj.org/article/44f5d1173322450ba374171242e3e64bTest

المؤلفون: Chen, S.¹, He, S.¹, Shi, X.‐H.¹, Shen, X.‐J.², Liang, K.‐K.¹, Zhao, J.‐H.¹, Yan, B.‐C.¹ ybch76@163.com, Zhang, J.‐W.¹ zhangjiewen9900@126.com

المصدر: Acta Neurologica Scandinavica. Aug2018, Vol. 138 Issue 2, p151-155. 5p.

مصطلحات موضوعية: *FATAL familial insomnia, *GENETIC mutation, *INSOMNIA, *MAGNETIC resonance imaging of the brain, *ELECTROENCEPHALOGRAPHY, *DIAGNOSIS

المؤلفون: Eryk Mikos, Sara Moqbil, Joanna Dmochowska, Martyna Wasyluk, Wanesa Góralczyk

المصدر: Journal of Education, Health and Sport, Vol 12, Iss 7 (2022)

مصطلحات موضوعية: fatal familial insomnia, diagnostic methods, polysomnography, imaging tests, cerebrospinal fluid biomarkers, Education, Sports, GV557-1198.995, Medicine

وصف الملف: electronic resource

العلاقة: https://apcz.umk.pl/JEHS/article/view/39152Test; https://doaj.org/toc/2391-8306Test

الوصول الحر: https://doaj.org/article/1c0944d5a1ea4cbeb21a47d95d69b892Test