Neurobiology of Aging and the Diagnosis of Generalized Degenerative Dis

The neurological deficits of aging may be viewed from a organic evolutional perspective. That is, the decline in functional efficiency and deterioration of highly narrow down non-dividing neuronal cells is the mop up point of a maturation process that occurs throughout adult life. Involution to senescence is a normal, inevitable, and inexorable physiological march the end phase of which is expressed in generally predictable and specifically unpredictable ways. The earliest of these developmental changes occurs long before senescence and the effects of these physiological events quiet accumulate toward expression late in life. There is a relationship between chronological age and the developmental dimensions of human life, including behavior and intelligence. This relationship begins at conception, and is at that point the only moment when in that location is exact correspondence between chronology and development. Afterwards, behavior or structural differentiation have shifting persona points one with some structural differentiation or performance milestone already achieved, the other with the time chronology (age) of the organism. Development refers to a continuum of lifelong biological and psychological processes. Neurological development along the biological scale is swift and complex during the prenatal period and small units of time constitute considerable change. In infancy, there is less neurological change as compared to prenatal development, but it is considerably more than those changes that occur in adult life. Indeed, in adult life, neurological development largely constitutes a diminution in function. Nonetheless, until the onset of senescence, in the absence of organic brain pathology, psychological development and learning co... ...otein and the neurofibrillary pathology of Alzheimers disease. TINS. 1993 16 (11) 460-465. 5.Goldman, J., Cote, L. agedness of the Brain Dementia of the Alzheimers Type. Chapter 62 (reference incomplete). 6.Han sen, L. A. Deteresa, R. Davies, P. I., and Terry, R. D. Neocortical morphometry, lesion counts, and choline acetyl-transferase levels in the age spectrum of Alzheimers disease. Neurology, 38 48-54. 7. Human, B. T., Van Hoesen, G.W., Damasio, A. R. and Barnes, C. L. Alzheimers disease Cell specific pathology isolates the hippocampal formation. Science, 225 1168-1170. 8. Miyakawa, T., Katsuragi, K., Yamashita, K., Ohuchi, K. geomorphological study of amyloid fibrils and preamyloid deposits in the brain with Alzheimers disease. Acta Neuropathologica, 1992 83 340-346. 9. Rossor, M. Alzheimers disease. Brit. Med. J., 1993 321 779-782.