Zobrazeno 1 - 10
of 613
pro vyhledávání: '"Rapidly progressive dementia"'
Publikováno v:
Prion, Pp 1-7 (2024)
Rapidly progressive dementias (RPDs) are a type of fatal dementias that cause rapid progression of neuronal dysfunction. This study aimed to assess the prevalence of APOE genotypes (ε2, ε3, ε4) and PRNP mutations (E200K, M129V) in the general popu
Externí odkaz:
https://doaj.org/article/1a0d9277e4924abfb920c940675928b7
Publikováno v:
Radiology Case Reports, Vol 20, Iss 2, Pp 1095-1098 (2025)
Creutzfeldt–Jakob Disease (CJD) is a rare, fatal neurodegenerative disorder that is caused by prion proteins. Patients often present with rapidly progressive dementia, ataxia, myoclonus, memory impairment, visual problems, and changes in personalit
Externí odkaz:
https://doaj.org/article/8c4d36ac3e36456d978ef890c2cc26c6
Autor:
Giuseppe Mario Bentivenga, Simone Baiardi, Andrea Mastrangelo, Edoardo Ruggeri, Angela Mammana, Alice Ticca, Marcello Rossi, Sabina Capellari, Piero Parchi
Publikováno v:
Alzheimer’s Research & Therapy, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background The term rapidly progressive dementia (RPD) with Lewy bodies (rpDLB) is used for DLB patients who develop a rapidly progressive neurological syndrome and have reduced survival. Here, we characterise the clinical, neuropathological
Externí odkaz:
https://doaj.org/article/ef9e0e17a9784355bde2bcad2168bd17
Autor:
Yu. A. Shpilyukova, A. O. Protopopova, N. Yu. Abramycheva, E. Yu. Fedotova, S. N. Illarioshkin
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 15, Iss 2, Pp 63-67 (2023)
Rapidly progressive dementias are a rare group of cognitive disorders that primarily require the exclusion of a large number of potentially reversible causes. Prion diseases are frequent in this group of disorders. Some hereditary forms of Alzheimer'
Externí odkaz:
https://doaj.org/article/9bea524e01934c9690747350b90495e2
Autor:
Xiaoyan Liu, Yan Sun, Xuyan Zhang, Ping Liu, Kan Zhang, Lihua Yu, Yujie Su, Yuan Yuan, Qing Ke, Guoping Peng
Publikováno v:
BMC Geriatrics, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Rapidly progressive dementia (RPD) is a syndrome originating from various diseases. Recent advances have allowed a better understanding of its categories and spectrum; however, it remains challenging to make an accurate differenti
Externí odkaz:
https://doaj.org/article/895821d3d10b444da151c3bb957532ac
Autor:
Carlos Andrés Clavijo, Ana María Portilla Buenaventura, Galo Santiago Benavides Albornoz, Juan José Muñoz Cabrera, María Camila Murillo Reyes, Alejandra Chauvez Gallego, Carlos Alberto Hurtado González, Sebastian Ospina Otalvaro, Carlos Steven Marmolejo Escobar, Karen Julieth Quebrada Mera, Paola Andrea Gutiérrez Lenis, Lina María Arango García, Armando Lucumí
Publikováno v:
Case Reports in Neurology, Vol 14, Iss 3, Pp 441-455 (2022)
Rapidly progressive dementia (RPD) is a heterogeneous group of diseases characterized by cognitive impairment and other neurological disorders developed in a short span of fewer than 2 years. Currently viewed as new and infrequent entities, most medi
Externí odkaz:
https://doaj.org/article/6c4cab18ce2441a5bc67a29339f4b252
Publikováno v:
PCN Reports, Vol 2, Iss 3, Pp n/a-n/a (2023)
Abstract Background Dementia that advances subacutely without accompanying neurological symptoms can often be misdiagnosed as a psychiatric condition. Leptomeningeal metastasis (LM), caused by the spread of malignant cells to the leptomeninges and th
Externí odkaz:
https://doaj.org/article/5737dc0cc22e4a53a4e7f17a8dc61707
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