منابع مشابه
Investigations of E.E.G. findings in presenile dementia.
The diagnosis of presenile dementia is used in its widest sense. Clinically, it is impossible to distinguish between the various neuropathological subgroups that make up this group of dementias. The exact diagnosis is only ascertained at death, although biopsies may be diagnostically useful. There appears to be considerable doubt about the E.E.G. findings in this group of patients. Hill (1948),...
متن کاملNeuropathological findings and staging in dementia
Dementia is a clinical syndrome with the development of impairment in multiple cognitive functions (including memory), severe enough to interfere with activities of daily living, as the main symptom. There are a large number of disorders that can lead to dementia, and neuropathological examination after death is necessary to determine the underlying cause with certainty. The overall aim of this...
متن کاملEPIDEMIOLOGICAL, CLINICAL AND ELECTRODIAGNOSTIC FINDINGS IN CHILDHOOD GUILLAIN-BARRE SYNDROME
In order to identify the clinical and electrophysiological characteristics of childhood Guillain-Barre Syndrome (GBS) in East Azarbaijan province, clinical and electrophysiological data on 40 consecutive children with GBS, admitted to Tabriz Children's Medical Center from March 21st 1999 to March 20th 2002, were analyzed. All patients received intravenous immunoglobulin, 400 mg /kg/ day fo...
متن کاملAccuracy of clinical diagnosis in primary degenerative dementia: correlation with neuropathological findings.
Neuropathological features and causes of death are presented in 27 deceased patients belonging to a prospective series of 71 hospitalised patients with primary degenerative dementia. The clinical criteria for primary degenerative dementia used in the present study were accurate enough to exclude patients with multi-infarct dementia. At necropsy, 82% of the cases had neuropathological changes of...
متن کاملClinical findings in Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies.
Dr. Luís Fabiano Marin – Rua Maranhão 192 / 101 01240-000 São Paulo SP Brasil. E-mail: [email protected] Creutzfeldt-Jakob disease (CJD) is a transmissible spongiform encephalopathy or prionic disease characterized by accumulation of abnormal prionic protein (PrP) associated to spongiform degeneration of the brain. Although rare, CJD is the most common prionic disease in humans with an inc...
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ژورنال
عنوان ژورنال: Nuclear Medicine Seminars
سال: 2016
ISSN: 2149-6447
DOI: 10.4274/nts.2016.018