| Description |
1 online resource (438 pages) : color illustrations |
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text txt rdacontent |
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computer c rdamedia |
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online resource cr rdacarrier |
| Note |
Print version record. |
| Contents |
Cover; Contents; Contributors; Abbreviations; 1 Lessons from the study of natural experiments of hyperendemic foci of neurodegeneration; 2 The motor neurone diseases; 3 Amyotrophic lateral sclerosis-parkinsonism-dementia complex in the Kii Peninsula of Japan (Muro disease): a review on recent research and new concept; 4 The frontotemporal dementias: an overview; 5 Language profiles in amyotrophic lateral sclerosis; 6 Language impairment in amyotrophic lateral sclerosis from an historical review: kana and kanji versus alphabetical languages. |
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7 Amyotrophic lateral sclerosis with dementia: neuropsychological aspects8 Social cognition in frontotemporal dementia and amyotrophic lateral sclerosis; 9 Behavioural change in amyotrophic lateral sclerosis; 10 Cognition in amyotrophic lateral sclerosis; 11 Frontotemporal syndromes of primary lateral sclerosis; 12 Electrophysiological evaluation of lower motor neurone loss in amyotrophic lateral sclerosis; 13 Multimodality approach to neuroimaging in amyotrophic lateral sclerosis/frontotemporal dementia. |
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14 Using neuroimaging to understand brain-behaviour relationships in the context of motor neurone disease15 Amyotrophic lateral sclerosis and the frontotemporal dementias: using neuroimaging to quantitate disease progression; 16 Differentiating normal from pathological atrophy: when is frontotemporal atrophy normal?; 17 Cerebrospinal fluid-based biomarkers for amyotrophic lateral sclerosis; 18 Neuropathology of frontotemporal lobar degeneration; 19 The neuropathology of the motor neurone diseases; 20 Genetics of frontotemporal dementia; 21 Genetics of the MNDs. |
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22 Perturbed RNA metabolism in amyotrophic lateral sclerosis23 Alterations in tau metabolism in amyotrophic lateral sclerosis with cognitive impairment; 24 Transactive response DNA-binding protein of 43 kDa; 25 Progranulin; Index; A; B; C; D; E; F; G; H; I; J; K; L; M; N; O; P; R; S; T; U; V; W; Y. |
| Summary |
Over the past ten years, there has been an increasing recognition that syndromes of frontotemporal dysfunction (FTD) are a common occurrence in patients with amyotrophic lateral sclerosis (ALS). Such syndromes may be present in as many as 60% of patients with ALS. Conversely, the occurrence of motor neuron dysfunction in patients with clinically pure frontotemporal dementia is increasingly recognized. This suggests that to some extent there are overlap syndromes in which both ALSand FTD occur within the same individual. This volume summarizes the advances in our understanding of these two diso. |
| Bibliography |
Includes bibliographical references and index. |
| Subject |
Amyotrophic lateral sclerosis.
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Frontal lobes -- Diseases.
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Dementia.
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Amyotrophic Lateral Sclerosis |
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Dementia |
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Sclérose latérale amyotrophique.
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Lobes frontaux -- Maladies.
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Démence.
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HEALTH & FITNESS -- Diseases -- Alzheimer's & Dementia.
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MEDICAL -- Neurology.
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Amyotrophic lateral sclerosis
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Dementia
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Frontal lobes -- Diseases
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| Added Author |
Strong, Michael J.
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| Other Form: |
Print version: Amyotrophic lateral sclerosis and the frontotemporal dementias. Oxford : Oxford University Press, 2012 9780199590674 (OCoLC)781497156 |
| ISBN |
9780191637285 (electronic bk.) |
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0191637289 (electronic bk.) |
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9780199590674 (Cloth) |
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0199590672 (Cloth) |
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9781283713436 (MyiLibrary) |
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1283713438 (MyiLibrary) |
| Standard No. |
AU@ 000058063180 |
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AU@ 000062595972 |
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