Handbook of cerebellar diseases
著者
書誌事項
Handbook of cerebellar diseases
（Neurological disease and therapy, v. 16）
M. Dekker, c1993
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注記
Includes bibliographical references and index
内容説明・目次
内容説明
This text examines the most common clinical disturbances affecting the cerebellum and examines disorders that appear to be related to this part of the brain, highlighting the impact of new neuro-imaging techniques and advances in molecular genetics. It provides many state-of-the-art computerized tomography and magnetic resonance illustrations, designed to familiarize the clinician with normal and abnormal cerebellar features.;Written by international authorities in the field, the Handbook of Cerebellar Diseases, amongst other things: details the signs and symptoms of hereditary disturbances of co-ordination, as well as their genetic bases and risks; presents exercises in molecular genetics that explain where the current investigations into hereditary degenerative diseases are leading; offers therapies, such as the management of cerebellar tumours and approaches to congenital anomalies, which take recent progress into account; covers slow-viral diseases, paraneoplastic disorders, vascular diseases, demyelination and toxic damage, and considers treatment options wherever they exist; and discusses tremors in-depth, as well as the clinical aspects of progressive ataxias.
目次
- Part 1 Background: history, Richard Lechtenberg and Colleen Blanchfield
- embryogenesis of the cerebellum, Richard Lechtenberg
- normal anatomy, Chandrakant Rao. Part 2 Diagnostics: signs and symptoms of cerebellar disease, Richard Lechtenberg
- origin and treatment of tremor in cerebellar disease, Jau-Shin Lou and Joseph Jankovic
- anatomic localization of tremor - clinical analysis, pitfalls, and principles, Louis T. Giron, Jr and William C. Koller
- neuroimaging studies of the cerebellum, David P.C. Liu
- positron emission tomographic studies of cerebellar disorders, Sid Gilman. Part 3 Structural disease: agenesis and hypoplasia, Richard Lechtenberg
- chiari malformations, Harvey S. Bennett
- Dandy-Walker malformation, John M. Pellock and Michele H. Johnson. Part 4 Neoplastic disease: cerebellar tumours, Kendra Peterson and Mark G. Malkin
- Von Hippel-Lindau disease, Sharon Hertz
- radiation therapy of cerebellar tumours, Hassan Aziz
- paraneoplastic cerebellar disorders, Edward J. Dropcho. Part 5 Vascular disease: cerebellar infarctions, Pierre Amarenco, et al
- cerebellar hemorrhage, Stephen Q. Shafer and John C.M. Brust
- cerebellar venous anatomy and disease, Lily Jung Eng and W.T. Longstreth, Jr
- transcranial doppler evaluation in vertebrobasilar disease, Shirley M. Otis. Part 6 Degenerative disease: distinguishing between the adult ataxias, Robert D. Currier and S. Harihara subramony
- Machado-Joseph disease - epidemiology, genetics, and genetic epidemiology, Jorge Sequeiros
- presumed Machado-Joseph disease - four kindreds from Mississippi, S. Harihara subramony, et al
- the Catarina kindred - Machado-Joseph disease of Azorean ancestry, Joao Radvany
- a common variety of hereditary ataxia in India, Noshir H. Wadia
- cerebellar synapses in hereditary ataxia, Craig G. Hurwitz and Arnulf H. Koeppen
- genetic heterogeneity of autosomal dominant ataxia, Stephen S. Rich
- a large family with autosomal dominant spinocerebellar ataxia - exclusion of linkage to SCA1, Alice M. Lazzarini, et al
- epidemiologic survey of hereditary ataxias and spastic paraplegias in Molise, Italy, Alessandro Filla, et al
- toward the isolation of the SCA1 gene on the short arm of human chromosome 6, Harry T. Orr, et al
- late-onset spinocerebellar ataxia in Calabria, Italy, Marina Frontali, et al
- linkage study of hereditary spinocerebellar atazias - evidence for genetic heterogeneity of dominant OPCA in Japan, H. Sasaki, et al
- anticipation of generations in dominant ataxias, Michael Wilensky
- Friedreich's disease, Bala V. Manyam
- cardiac iron deposits in Friedreich's ataxia, Jacques B. Lamarche, et al. Part contents.
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