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Results for “PSYCHOSES, PRESENILE”
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[On the problem of nosological types of dementia. (The nature of dementia in some atrophic demential presenile processes)].
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[Structure of mental diseases of the 2d half of life according to the results of an epidemiologic study].
An investigation of all patients (with the exception of alcoholics) residing in a city district and registered at a psychoneurological dispensary revealed that after 40 years the disease began in almost one-fourth of the cases (24.7%). In the majority of cases (56%) these were diseases characteristic of the second half of life: vascular pathology (45.3%), involutional psychoses (6.6%), presenile dementia (2.2%) and senile dementia (1.9%). Other findings included schizophrenia in 24.3%, manic-depressive psychoses in 2.7%, psychogenias in 7.6%, consequences of head trauma in 2.2% and other exogenias in 3.7%. The clinical and social parameters of the prognosis in mental diseases first expressed after 40 years of age were on the whole lower but they reflected the modern tendency to attenuation of pathological manifestations: by the time of examination the status of 48% of patients was characterized by intermission or syndromes of a nonpsychotic level.
[Memory disorders of the presenile climacteric].
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LIPID CLASS COMPOSITION OF NORMAL HUMAN BRAIN AND VARIATIONS IN METACHROMATIC LEUCODYSTROPHY, TAY-SACHS, NIEMANN-PICK, CHRONIC GAUCHER'S AND ALZHEIMER'S DISEASES.
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FATTY ACID COMPOSITIONS OF HUMAN BRAIN LECITHIN AND SPHINGOMYELIN IN NORMAL INDIVIDUALS, SENILE CEREBRAL CORTICAL ATROPHY, ALZHEIMER'S DISEASE, METACHROMATIC LEUCODYSTROPHY, TAY-SACHS AND NIEMANN-PICK DISEASES.
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CLINICAL AND PATHOLOGICAL CHARACTERISTICS IN WILSON'S DISEASE IN CASES UNDER TEN YEARS OF AGE.
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[ON A CASE OF CHRONIC, PREDOMINANTLY OPTIC, PRESENILE HALLUCINOSIS].
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[ON INVOLUTIONAL PSYCHOSIS AND PRESENILE DEMENTIA].
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[Clinical, biological, and electric studies on two cases of presenile atrophic dementia of true tropical etiology].
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[Presenile spongy brain atrophy].
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EXPERIMENTAL PRODUCTION OF NEUROFIBRILLARY DEGENERATION 2. ELECTRON MICROSCOPY, PHOSPHATASE HISTOCHEMISTRY AND ELECTRON PROBE ANALYSIS.
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SPECULATIONS ON THE NATURE OF THE METABOLIC DEFECTS IN TAY-SACHS, NIEMANN-PICK, GAUCHER'S AND ALZHEIMER'S DISEASES, AND METACHROMATIC LEUCODYSTROPHY.
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[AN AUTOPSY CASE OF PRESENILE DEMENTIA BELONGING TO THE CREUTZFELDT-JAKOB GROUP].
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[Clinical study of presenile dementia (Alzheimer's disease)].
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[VASCULAR PATHOLOGY AND ITS ROLE IN VARIOUS TYPES OF COURSE OF PRESENILE DEPRESSION].
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[Presenile or involution syndromes; clinical aspects and therapy].
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CHEMICAL STUDIES ON ALZHEIMER'S DISEASE.
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