نتایج جستجو برای: creutzfeldt

تعداد نتایج: 3390  

E. Poorakbar Poorakbar Karim Nikkhah, M. Saiedi R. Sadrenabavi

Creutzfeldt-Jacob disease is the most common form of prion diseases, which have become public health problems in the last two decades because of the high number of reported cases of mad cow disease in Great Britain and other countries. Creutzfeldt-Jacob disease is a fatal situation with known cardinal clinical features including progressive memory loss and myoclonic seizure disorder. In this re...

Journal: :iranian journal of medical sciences 0
karim nikkhah m. saiedi r. sadrenabavi e. poorakbar poorakbar

creutzfeldt-jacob disease is the most common form of prion diseases, which have become public health problems in the last two decades because of the high number of reported cases of mad cow disease in great britain and other countries. creutzfeldt-jacob disease is a fatal situation with known cardinal clinical features including progressive memory loss and myoclonic seizure disorder. in this re...

Journal: :Brain : a journal of neurology 2010
Ichiro Nozaki Tsuyoshi Hamaguchi Nobuo Sanjo Moeko Noguchi-Shinohara Kenji Sakai Yosikazu Nakamura Takeshi Sato Tetsuyuki Kitamoto Hidehiro Mizusawa Fumio Moriwaka Yusei Shiga Yoshiyuki Kuroiwa Masatoyo Nishizawa Shigeki Kuzuhara Takashi Inuzuka Masatoshi Takeda Shigetoshi Kuroda Koji Abe Hiroyuki Murai Shigeo Murayama Jun Tateishi Ichiro Takumi Susumu Shirabe Masafumi Harada Atsuko Sadakane Masahito Yamada

We analysed the epidemiological data and clinical features of patients with prion diseases that had been registered by the Creutzfeldt-Jakob Disease Surveillance Committee, Japan, over the past 10 years, since 1999. We obtained information on 1685 Japanese patients suspected as having prion diseases and judged that 1222 patients had prion diseases, consisting of definite (n=180, 14.7%) and prob...

Journal: :Brain : a journal of neurology 2010
Piero Parchi Maura Cescatti Silvio Notari Walter J Schulz-Schaeffer Sabina Capellari Armin Giese Wen-Quan Zou Hans Kretzschmar Bernardino Ghetti Paul Brown

Six clinico-pathological phenotypes of sporadic Creutzfeldt-Jakob disease have been characterized which correlate at the molecular level with the type (1 or 2) of the abnormal prion protein, PrP(TSE), present in the brain and with the genotype of polymorphic (methionine or valine) codon 129 of the prion protein gene. However, to what extent these phenotypes with their corresponding molecular co...

2014
Zhe Kang Norlinah Mohamed Ibrahim

Creutzfeldt-Jakob disease is a rare, human transmissible prion disease which carries a grave prognosis with no specific treatment. Although widely reported in English literature, reports of Creutzfeldt-Jakob disease in Southeast Asia are scarce. The incidence of Creutzfeldt-Jakob disease in this region is unknown. This raises the question of whether Creutzfeldt-Jakob disease is actually rarer i...

2009
I. Zerr K. Kallenberg D. M. Summers C. Romero A. Taratuto U. Heinemann M. Breithaupt D. Varges B. Meissner A. Ladogana M. Schuur S. Haik S. J. Collins Gerard H. Jansen G. B. Stokin J. Pimentel E. Hewer D. Collie P. Smith H. Roberts J. P. Brandel C. van Duijn M. Pocchiari C. Begue P. Cras R. G. Will P. Sanchez-Juan

Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrated a potentially important role for magnetic resonance imaging in the pre-mortem diagnosis of spo...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1984
S Gálvez L Cartier

Computed tomography (CT) was normal in twelve of fifteen patients with definite Creutzfeldt-Jakob disease. In two patients CT showed mild sulcal widening, while marked ventricular enlargement and moderate cortical atrophy were seen in a patient who had both Creutzfeldt-Jakob disease and normal pressure hydrocephalus. No correspondence was observed between CT findings, severity of the clinical p...

2014
Jae-Won Jang So Young Park Young Ho Park Jung E Kim SangYun Kim

BACKGROUND Creutzfeldt-Jakob disease and Hashimoto's encephalopathy often show similar clinical presentation. Among Creutzfeldt-Jakob disease mimics, Hashimoto's encephalopathy is particularly important as it is treatable with corticosteroids. Thus, in cases of middle-aged woman diagnosed with probable Creutzfeldt-Jakob disease and who exhibit high titers of antithyroid antibodies, corticostero...

2012

case-control studies. Neurology 1996;46: 1287–91. 5 Alperovitch A, Zerr I, Pocchiari M, Mitrova E, et al. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease. Lancet 1999;353:1673–4. 6 Pocchiari M. Prions and related neurological diseases. Mol Aspects Med 1994;15:195–291. 7 Brown P, Goldfarb LG, Kovanen J, Haltia M, et al. Phenotypic characteristics of familial Creutzfeldt-J...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2010
K F Ko W Y Lau W K Cheng M C Kwan L K Yip

The early stage of sporadic Creutzfeldt-Jakob disease is generally characterised by progressive changes in behaviour and intellectual function. While only a few patients have stroke-like onset, Creutzfeldt-Jakob disease with initial monoparesis has been described. In this report, a patient with an unusual sporadic Creutzfeldt-Jakob disease with typical magnetic resonance imaging findings, posit...

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