نتایج جستجو برای: jakob disease

تعداد نتایج: 1490898  

Journal: :iranian journal of neurology 0
nasim tabrizi department of neurology, school of medicine, mazandaran university of medical sciences, sari, iran. mahmoud abedini department of neurology, school of medicine, mazandaran university of medical sciences, sari, iran.

no abstract

Background: Creutzfeldt-Jakob disease (CJD) as a life-threatening neurodegenerative disorder is not usually diagnosed in early stages of the disease because of a variety in its clinical manifestations. This study aimed to present a middle-aged woman with psychiatric symptoms who ultimately was diagnosed as a CJD case. Case presentation: This 48-year-old woman had progressive symptoms of depres...

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: :Journal of Clinical Pathology 1972

Journal: :European Neurology 2004

Journal: :Continuing Education in Anaesthesia Critical Care & Pain 2013

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...

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...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید