Zobrazeno 1 - 10
of 767
pro vyhledávání: '"sporadic creutzfeldt-jakob disease"'
Autor:
Sachiko Koyama, Kaoru Yagita, Hideomi Hamasaki, Hideko Noguchi, Masahiro Shijo, Kosuke Matsuzono, Kei-Ichiro Takase, Keita Kai, Shin-Ichi Aishima, Kyoko Itoh, Toshiharu Ninomiya, Naokazu Sasagasako, Hiroyuki Honda
Publikováno v:
Prion, Vol 18, Iss 1, Pp 40-53 (2024)
Prion disease is an infectious and fatal neurodegenerative disease. Western blotting (WB)-based identification of proteinase K (PK)-resistant prion protein (PrPres) is considered a definitive diagnosis of prion diseases. In this study, we aimed to de
Externí odkaz:
https://doaj.org/article/88736088322f420ebc3eef6459d81384
Publikováno v:
CHRISMED Journal of Health and Research, Vol 11, Iss 1, Pp 67-70 (2024)
Creutzfeldt–Jakob disease (CJD) is a rare, progressive, and fatal disease. Sporadic CJD (sCJD) accounts for 85% of the CJD cases. It is characterized by rapidly progressive dementia, myoclonic jerks, and pyramidal, extrapyramidal, visual, and psych
Externí odkaz:
https://doaj.org/article/ebed3a3f43bf4ef6a860b04a735f9935
Publikováno v:
Acta Medica Bulgarica, Vol 51, Iss s1, Pp 36-40 (2024)
Sporadic Creutzfeldt–Jakob disease is a rare and fatal human prion disease characterized by a rapidly progressive dementia, myoclonus, cerebellar, pyramidal, extrapyramidal, visual, and psychiatric symptoms. These findings are all non-specific and
Externí odkaz:
https://doaj.org/article/5a70f792b11d4864b5315f90d65b1f0c
Autor:
Hoang Dinh Au, MD, PhD, Nguyen Thu Lan, MD, Nguyen Thai Binh, MD, PhD, Le Tuan Linh, MD, PhD, Ma Mai Hien, MD, Nguyen Minh Duc, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 3, Pp 939-943 (2024)
Sporadic Creutzfeldt-Jakob disease (sCJD) is an uncommon prion disease, also a fatal degenerative brain disorder. We aimed to illustrate 2 clinical cases, a 60-year-old female and a 57-year-old male, who came to the hospital due to rapidly progressiv
Externí odkaz:
https://doaj.org/article/02ea5f52f7144973b6e90b999cff278e
Autor:
Toshiaki Nonaka, Ryusuke Ae, Koki Kosami, Hiroya Tange, Miho Kaneko, Takehiro Nakagaki, Tsuyoshi Hamaguchi, Nobuo Sanjo, Yoshikazu Nakamura, Tetsuyuki Kitamoto, Yoshiyuki Kuroiwa, Kensaku Kasuga, Manabu Doyu, Fumiaki Tanaka, Koji Abe, Shigeo Murayama, Ichiro Yabe, Hideki Mochizuki, Takuya Matsushita, Hiroyuki Murai, Masashi Aoki, Koji Fujita, Masafumi Harada, Masaki Takao, Tadashi Tsukamoto, Yasushi Iwasaki, Masahito Yamada, Hidehiro Mizusawa, Katsuya Satoh, Noriyuki Nishida
Publikováno v:
Diagnostics, Vol 14, Iss 21, p 2424 (2024)
Background/Objectives: Sporadic Creutzfeldt–Jakob disease (sCJD) is a fatal neurodegenerative disorder traditionally diagnosed based on the World Health Organization (WHO) criteria in 1998. Recently, Hermann et al. proposed updated diagnostic crite
Externí odkaz:
https://doaj.org/article/1d7e4d35198745628c5f312cf6064510
Autor:
Jiangfeng Liao, Wenming Hu, Shiheng Chen, Chunyu Huang, Senwei Dong, Wanjin Chen, Xiaochun Chen, Longfei Chen
Publikováno v:
Frontiers in Aging Neuroscience, Vol 16 (2024)
BackgroundAs a rare neurodegenerative disease, sporadic Creutzfeldt-Jakob disease (sCJD) is poorly understood in the elderly populace. This study aims to enunciate the multidimensional features of sCJD in this group.MethodsA case of probable sCJD was
Externí odkaz:
https://doaj.org/article/58926469b5aa4d1688ab4f1063d1c880
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-5 (2023)
Abstract Background Creutzfeldt–Jakob disease (CJD), is a deadly degenerative condition of the central nervous system marked by rapidly progressive dementia. Magnetic resonance imaging (MRI) abnormalities in the cerebral cortex, basal ganglia, thal
Externí odkaz:
https://doaj.org/article/724106091c6d4a73938178c85ed19c3b
Autor:
Taha K. Alloush, Adel T. Alloush, Yaser Abdelazeem, Hossam M. Shokri, Khaled O. Abdulghani, Ahmed Elzoghby
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 59, Iss 1, Pp 1-7 (2023)
Abstract Background Creutzfeldt–Jakob disease (CJD) is a rare, fatal neurodegenerative disorder, with few months as a usual duration from onset to death. Case presentation In this case report, a patient of Sporadic CJD (sCJD) who presented one mont
Externí odkaz:
https://doaj.org/article/b4a6ef6f92b44f53b771fa1ef0d563bf
Autor:
Martina Tarozzi, Simone Baiardi, Claudia Sala, Anna Bartoletti-Stella, Piero Parchi, Sabina Capellari, Gastone Castellani
Publikováno v:
Acta Neuropathologica Communications, Vol 10, Iss 1, Pp 1-16 (2022)
Abstract Creutzfeldt-Jakob disease (CJD) is characterized by a broad phenotypic spectrum regarding symptoms, progression, and molecular features. Current sporadic CJD (sCJD) classification recognizes six main clinical-pathological phenotypes. This wo
Externí odkaz:
https://doaj.org/article/b4585135c22d40e79e1c72d90d5391b1
Publikováno v:
Prion, Vol 16, Iss 1, Pp 91-94 (2022)
Creutzfeldt-Jakob disease (CJD) is a low-prevalence, fatal neurodegenerative disease. Parkinsonism as first symptom of CJD is rare. We present a case manifesting difficulty falling asleep as unspecific prodromal symptom and parkinsonism as initial sy
Externí odkaz:
https://doaj.org/article/01f0ea16b2504b1f991a4fe8a6cf948c