SA Cooper, KL Murray, CA Heath, RG Will, … - British Medical Journal, 2006 - jnnp.bmj.com Results: 29 of 618 (5%) patients with sCJD had an isolated cerebellar onset.
Mean illness duration was 9 months. Subsequently, 21 (72%) developed myoclonus
and 23 (79%) developed pyramidal features. Magnetic resonance imaging ... Cited by 11 - Related articles - BL Direct - All 5 versions
I Nozaki, T Hamaguchi, M Noguchi-Shinohara, … - Neurology, 2006 - pt.wkhealth.com From the Department of Neurology and Neurobiology of Aging (IN, TH, MN-S., KO,
KK, MY), Kanazawa University Graduate School of Medical Science, Kanazawa;
Department of Neurology (HS), Tonami General Hospital, Tonami; and ... Cited by 9 - Related articles - BL Direct - All 4 versions
HS Kirshner, PJM Lavin - Current Neurology and Neuroscience Reports, 2006 - Springer Introduction Posterior cortical atrophy, also called progressive posterior
cortical dysfunction [1••], is a focal dementing disorder characterized by
progressive visual symptoms and signs of cortical origin that may initially ... Cited by 7 - Related articles - BL Direct - All 2 versions
T Hamaguchi, M Noguchi-Shinohara, Y …, 2007 - pubmedcentral.nih.gov Eleven (1.8%) of 597 patients underwent ophthalmic surgery within 1 month before
the onset of prion disease or after the onset. All ophthalmologists reused
surgical instruments that had been incompletely sterilized to eliminate ... Cited by 3 - Related articles - BL Direct - All 5 versions
- ►umsha.ac.ir [PDF] R Wada, W Kucharczyk - Neuroimaging Clinics of North America, 2008 - Elsevier Prions are a rare cause of human disease but very important to recognize because
of their potential for transmissibility and uniformly severe outcome. MR imaging
plays an extremely important role in early diagnosis, especially with ... Cited by 1 - Related articles - All 8 versions
A Ishikawa, A Tanikawa, Y Shimada, T Mutoh … - Japanese Journal of Ophthalmology, 2009 - Springer We examined three cases of CJD with visual distur- bances.The first patient had
initially visited our ophthalmol- ogy department complaining of blurred vision,
and the ERG changes were detected before she was diagnosed with CJD. 6 The ... Related articles - All 2 versions
J Kanazawa - origin.cdc.gov Visual impairment occurs in 10% to 20% of patients with sporadic
Creutzfeldt-Jakob disease (sCJD) dur- ing an early stage of the disease
(Heidenhain variant) (1,2). Some patients with prion diseases may visit ... Related articles - View as HTML - All 2 versions
J Rachinger, F Aichner, S Weis, R Pichler, J … - Clinical Neuroradiology, 2007 - Springer Introduction Creutzfeldt-Jakob disease (CJD) belongs to the group of
transmissible human spongiform encephalopathies. It is a very rare
neurodegenerative disease of the brain, which occurs in humans as genetic, ... Related articles - BL Direct
MW Head, JW Ironside - Expert Review of Ophthalmology, 2008 - ingentaconnect.com Creutzfeldt–Jakob disease (CJD) belongs to the group of human prion diseases
– rare neurodegenerative disorders that are caused by transmissible agents
known as prions. In CJD, the levels of prion infectivity are highest in the ... Related articles - All 3 versions
