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

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

الوصول الحر: https://doaj.org/article/cfc9188dd6af410a8e6bdf60e5be378fTest

المؤلفون: Sarosh M Katrak, Apoorva Pauranik, Shrinivas B Desai, Simon Mead, Jon Beck, Sebastian Brandner, John Collinge

المصدر: Annals of Indian Academy of Neurology, Vol 22, Iss 4, Pp 458-461 (2019)

مصطلحات موضوعية: d178n mutation, familial creutzfeldt jakob disease, presenile dementia, protracted course, spongiform degeneration, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: http://www.annalsofian.org/article.asp?issn=0972-2327;year=2019;volume=22;issue=4;spage=458;epage=461;aulast=KatrakTest; https://doaj.org/toc/0972-2327Test; https://doaj.org/toc/1998-3549Test

الوصول الحر: https://doaj.org/article/ab89a9d73ec84d31a729636a970f1b94Test

المؤلفون: Katrak, S, Pauranik, A, Desai, S, Mead, S, Beck, J, Brandner, S, Collinge, J

المصدر: Annals of Indian Academy of Neurology , 22 (4) pp. 458-461. (2019)

مصطلحات موضوعية: D178N mutation, familial Creutzfeldt Jakob Disease, presenile dementia, protracted course, spongiform degeneration

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10086554/1Test/Familial%20Creutzfeldt-Jakob%20Disease%20in%20an%20Indian%20Kindred.pdf; https://discovery.ucl.ac.uk/id/eprint/10086554Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10086554/1Test/Familial%20Creutzfeldt-Jakob%20Disease%20in%20an%20Indian%20Kindred.pdf
https://discovery.ucl.ac.uk/id/eprint/10086554Test/

المؤلفون: Simon Mead, Shrinivas B Desai, Jon Beck, Sarosh M Katrak, Sebastian Brandner, John Collinge, Apoorva Pauranik

المصدر: Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 22, Iss 4, Pp 458-461 (2019)

مصطلحات موضوعية: animal diseases, Disease, medicine.disease_cause, Genetic analysis, lcsh:RC346-429, PRNP, 03 medical and health sciences, 0302 clinical medicine, protracted course, spongiform degeneration, medicine, Missense mutation, 030212 general & internal medicine, D178N mutation, presenile dementia, Gene, lcsh:Neurology. Diseases of the nervous system, Genetics, Mutation, business.industry, familial Creutzfeldt Jakob Disease, nervous system diseases, Gliosis, Familial Creutzfeldt-Jakob, Original Article, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be78129e82b510f0eab01d4661443c80Test
http://europepmc.org/articles/PMC6839320Test

المؤلفون: P. Nataraja, Bala Balaji, Alfred Stenwin Sunny, Albert Stezin, Naveen Thota

المصدر: Acta Scientific Neurology. 4:15-18

مصطلحات موضوعية: Genetics, Economics and Econometrics, business.industry, Anticipation (genetics), Materials Chemistry, Media Technology, Familial Creutzfeldt-Jakob, Medicine, Forestry, Disease, business, Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::93ca0470f93cff29d8891ab43c6ee5f0Test
https://doi.org/10.31080/asne.2021.04.0330Test

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

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

مصطلحات موضوعية: 0301 basic medicine, prnp gene, e200k, medicine.medical_specialty, lcsh:QH426-470, Biology, Creutzfeldt-Jakob Syndrome, Applied Microbiology and Biotechnology, Dermatology, nervous system diseases, lcsh:Genetics, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, cjd in patagonia, mental disorders, Genetics, medicine, familial creutzfeldt-jakob syndrome, 030217 neurology & neurosurgery, Genetics (clinical), Biotechnology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18ec866c54540f6141b5d266ebfb0e40Test
https://doi.org/10.35407/bag.2020.31.01.01Test

المؤلفون: Joab Chapman, Shmuel Appel, Michael Osherov, Zeev Nitsan, Hanna Rosenmann, Amos D. Korczyn, Ron Milo, Oren S. Cohen, Esther Kahana

المصدر: Journal of Neurology. 267:2455-2458

مصطلحات موضوعية: medicine.medical_specialty, Pediatrics, Neurology, business.industry, Disease, 03 medical and health sciences, 0302 clinical medicine, Cerebrospinal fluid, Frontal lobe, medicine, Familial Creutzfeldt-Jakob, 030212 general & internal medicine, Neurology (clinical), Age of onset, Cognitive decline, business, 030217 neurology & neurosurgery, Neuroradiology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::4d8c171f63d9b824c78aa9e700c5cbf8Test
https://doi.org/10.1007/s00415-020-09826-zTest

المؤلفون: Donglai Jing, Yaojing Chen, Kexin Xie, Yue Cui, Chunlei Cui, Li Liu, Hui Lu, Jing Ye, Ran Gao, Lin Wang, Zhigang Liang, Zhanjun Zhang, Liyong Wu

المصدر: Frontiers in Aging Neuroscience, Vol 13 (2021)
Frontiers in Aging Neuroscience

مصطلحات موضوعية: Aging, Pathology, medicine.medical_specialty, Cognitive Neuroscience, Creutzfeldt–Jakob disease, preclinical stage, Neurosciences. Biological psychiatry. Neuropsychiatry, White matter, 03 medical and health sciences, 0302 clinical medicine, Gyrus, mental disorders, Fractional anisotropy, medicine, 030212 general & internal medicine, Original Research, business.industry, Superior longitudinal fasciculus, Neuropsychology, diffusion tensor imaging, medicine.anatomical_structure, tract-based spatial statistics, Familial Creutzfeldt-Jakob, business, white matter, Asymptomatic carrier, 030217 neurology & neurosurgery, Neuroscience, RC321-571, Diffusion MRI

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f27da53021430b93bec445a66038726eTest
https://doi.org/10.3389/fnagi.2021.655667Test

المؤلفون: Huang, Nancy, Marie, Suely K.N., Kok, Fernando, Nitrini, Ricardo

المصدر: Arquivos de Neuro-Psiquiatria. December 2001 59(4)

مصطلحات موضوعية: familial Creutzfeldt-Jakob disease, prion protein gene mutation, codon 210, 14-3-3 protein

وصف الملف: text/html

الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2001000600017Test

المؤلفون: L. Saitta, Paola Mandich, Giacomo Boffa, Nicola Romano, Marina Grandis, G. L. Mancardi, Caterina Lapucci, Flavio Nobili

المصدر: The Open Neurology Journal. 13:72-75

مصطلحات موضوعية: Psychiatry and Mental health, medicine.medical_specialty, Neurology, Creutzfeldt Jacob Disease, business.industry, mental disorders, medicine, Familial Creutzfeldt-Jakob, Neurology (clinical), Multiple cranial neuropathy, Disease, business, Dermatology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b6d0f01df6463afad3acdf7508bc1b52Test
https://doi.org/10.2174/1874205x01913010072Test