Listing 1 - 2 of 2 |
Sort by
|
Choose an application
In this volume, the researchers focus on the interactions of frontotemporal dementia patients. These patients have right hemisphere, frontal and temporal pole atrophy which leaves their cognitive abilities intact, but their social interactions impaired and their personalities changed. The volume opens with a discussion of the frontal lobes and their expected contributions to language as a tool for social interaction. Then a conversation analytic approach is applied to analyze what changes in the structure of interaction lead to a sense that the interactions are impaired or inappropriate. Finally, the volume ends with a look forward to what FTD contributes to our understanding of human sociality and what has been gained in our understanding of the brain and language.
Taal --- Dementie --- Language and languages --- Neurolinguistics. --- Frontotemporal dementia --- Dementia, Frontotemporal --- Disinhibition-Dementia-Parkinsonism-Amyotrophy complex --- FLDEM (Frontotemporal lobe dementia) --- Frontotemporal lobe dementia --- FTD (Frontotemporal dementia) --- Hereditary dysphasic disinhibition dementia --- Wilhelmsen-Lynch disease --- Presenile dementia --- Neuro-linguistics --- Biolinguistics --- Higher nervous activity --- Neuropsychology --- Neurophysiology --- Physiological aspects. --- Pathophysiology. --- Therapie --- Kleuter --- Geschiedenis --- Spraaktechnologie --- Dementia --- Frontotemporal Dementia --- Interpersonal Relations. --- Speech --- Psychology. --- Physiology.
Choose an application
Under the name of Frontotemporal Dementias (FTD) numerous hereditary and sporadic disorders are listed. FTD may take away speech and language, social skills and ethical judgement, wishes and will, empathy and emotions; it may also impair motor functions. FTD may affect men and women in midlife or during old age leading to the demolition of the uniqueness of the human mind. In the last decade of the 20th century and in the first two decades of the 21st century, progress in the understanding of clinical, neuropathological, biochemical, and genetic aspects of FTD has accelerated. The novel awareness about FTD has directed young generations of researchers toward the study of this complex group of disorders. This Volume has been formulated with the participation of some of the leading scientists who have contributed to the development of knowledge in the clinical and basic science arenas. It captures the current central elements that are relevant to an up-to-date understanding of causes and pathogenesis of multiple forms of FTD. The volume is an opus that represents a distillation of the work of many scientists and addresses the current directions in the study of one of the most complex groups of diseases. In view of its structure, the book could also be used as a textbook, that offers both a broad and deep analysis of major areas in FTD. This book, planned by the International Society for Frontotemporal Dementias, is distinctive as it opens a window to a wide landscape about the biology of FTD. Thus, the book represents a moment of reflection on the present state of our knowledge of FTD and a collective vision toward scientific progress. The authors of each chapter share their knowledge and vision aimed at reducing the suffering which is caused by FTD.
Neurosciences. --- Neurology . --- Human genetics. --- Neurology. --- Human Genetics. --- Genetics --- Heredity, Human --- Human biology --- Physical anthropology --- Medicine --- Nervous system --- Neuropsychiatry --- Neural sciences --- Neurological sciences --- Neuroscience --- Medical sciences --- Diseases --- Frontotemporal dementia. --- Dementia, Frontotemporal --- Disinhibition-Dementia-Parkinsonism-Amyotrophy complex --- FLDEM (Frontotemporal lobe dementia) --- Frontotemporal lobe dementia --- FTD (Frontotemporal dementia) --- Hereditary dysphasic disinhibition dementia --- Wilhelmsen-Lynch disease --- Presenile dementia --- Medical genetics. --- Neuroscience. --- Medical Genetics. --- Clinical genetics --- Heredity of disease --- Human genetics --- Pathology --- Genetic disorders --- Genetic aspects
Listing 1 - 2 of 2 |
Sort by
|