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Ataxic disorders [electronic resource]

Ataxic disorders [electronic resource]

자료유형
E-Book(소장)
개인저자
Subramony, Sankara H. Durr, Alexandria.
서명 / 저자사항
Ataxic disorders [electronic resource] / volume editors, Sankara H. Subramony and Alexandria Durr.
발행사항
Edinburgh :   Elsevier,   2012.  
형태사항
1 online resource (xiv, 663 p.) : ill. (some col.).
총서사항
Handbook of clinical neurology ;3rd ser., v. 103
ISBN
9780444534941 (electronic bk.) 0444534946 (electronic bk.)
요약
"This volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new neurophysiological and imaging techniques are discussed, along with an in-depth examination of the treatment and management protocols of ataxic diseases."--Publisher's website.
일반주기
Title from e-Book title page.  
내용주기
Basic aspects. The cerebellum -- structure and connections ; Physiology of clinical dysfunction of the cerebellum ; Oculomotor aspects of the hereditary cerebellar ataxias ; Magnetic resonance and nuclear medicine imaging studies in ataxic disease ; Neuropathology of degenerative ataxias ; Approach to ataxic diseases. -- Acquired ataxias. Acquired ataxias, infectious and para-infectious ; Ataxia in patients with brain infarcts and hemorrhages ; Ataxia resulting from posterior fossa tumors of childhood and other mass lesions ; Nutritional cerebellar degeneration, with comments on its relationship to Wernicke disease and alcoholism ; Immune-mediated acquired ataxias ; Toxic agents causing cerebellar ataxias ; Paraneoplastic cerebellar degeneration. -- Degenerative ataxias. Epidemiology and population genetics of degenerative ataxias ; Sporadic adult onset ataxia of unknown aetiology. Degenerative ataxias -- Mitochondrial, autosomal recessive and x-linked. Overview of autosomal recessive ataxias ; Friedrich's ataxia ; Ataxia with vitamin E deficiency and abetalipoproteinemia ; Ataxia-telangiectasia ; Autosomal recessive cerebellar ataxias with oculomotor apraxia ; Other autosomal recessive and childhood ataxias ; Ataxia in mitochondrial disorders ; Fragile X-associated tremor/ataxia syndrome. -- Degenerative ataxias -- autosomal dominant. Overview of autosomal dominant ataxias ; Spinocerebellar ataxia type 1, 2 ; Machado-Joseph disease/spinocerebellar ataxia type 3 ; Spinocerebellar ataxia type 5, 6, 7 ; Clinical and genetic features of spinocerebellar ataxia type 8 ; Spinocerebellar ataxia type 10, 11, 12, 13, 14, 15, 20, 25, 28 ; Other spinocerebellar ataxias ; Dentatorubral-pallidoluysian atrophy ; Episodic ataxias 1 and 2. -- Other issues. Ataxias related to sensory neuropathies ; Frontal lobe ataxia ; Balance and gait problems in the elderly ; Treatment and management issues in ataxic disease.
서지주기
Includes bibliographical references and index.
이용가능한 다른형태자료
Issued also as a book.  
일반주제명
Ataxia. Movement disorders. Ataxia.
바로가기
ScienceDirect   URL
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245 0 0 ▼a Ataxic disorders ▼h [electronic resource] / ▼c volume editors, Sankara H. Subramony and Alexandria Durr.
260 ▼a Edinburgh : ▼b Elsevier, ▼c 2012.
300 ▼a 1 online resource (xiv, 663 p.) : ▼b ill. (some col.).
490 1 ▼a Handbook of clinical neurology ; ▼v 3rd ser., v. 103
500 ▼a Title from e-Book title page.
504 ▼a Includes bibliographical references and index.
505 0 ▼a Basic aspects. The cerebellum -- structure and connections ; Physiology of clinical dysfunction of the cerebellum ; Oculomotor aspects of the hereditary cerebellar ataxias ; Magnetic resonance and nuclear medicine imaging studies in ataxic disease ; Neuropathology of degenerative ataxias ; Approach to ataxic diseases. -- Acquired ataxias. Acquired ataxias, infectious and para-infectious ; Ataxia in patients with brain infarcts and hemorrhages ; Ataxia resulting from posterior fossa tumors of childhood and other mass lesions ; Nutritional cerebellar degeneration, with comments on its relationship to Wernicke disease and alcoholism ; Immune-mediated acquired ataxias ; Toxic agents causing cerebellar ataxias ; Paraneoplastic cerebellar degeneration. -- Degenerative ataxias. Epidemiology and population genetics of degenerative ataxias ; Sporadic adult onset ataxia of unknown aetiology. Degenerative ataxias -- Mitochondrial, autosomal recessive and x-linked. Overview of autosomal recessive ataxias ; Friedrich's ataxia ; Ataxia with vitamin E deficiency and abetalipoproteinemia ; Ataxia-telangiectasia ; Autosomal recessive cerebellar ataxias with oculomotor apraxia ; Other autosomal recessive and childhood ataxias ; Ataxia in mitochondrial disorders ; Fragile X-associated tremor/ataxia syndrome. -- Degenerative ataxias -- autosomal dominant. Overview of autosomal dominant ataxias ; Spinocerebellar ataxia type 1, 2 ; Machado-Joseph disease/spinocerebellar ataxia type 3 ; Spinocerebellar ataxia type 5, 6, 7 ; Clinical and genetic features of spinocerebellar ataxia type 8 ; Spinocerebellar ataxia type 10, 11, 12, 13, 14, 15, 20, 25, 28 ; Other spinocerebellar ataxias ; Dentatorubral-pallidoluysian atrophy ; Episodic ataxias 1 and 2. -- Other issues. Ataxias related to sensory neuropathies ; Frontal lobe ataxia ; Balance and gait problems in the elderly ; Treatment and management issues in ataxic disease.
520 ▼a "This volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new neurophysiological and imaging techniques are discussed, along with an in-depth examination of the treatment and management protocols of ataxic diseases."--Publisher's website.
530 ▼a Issued also as a book.
538 ▼a Mode of access: World Wide Web.
650 0 ▼a Ataxia.
650 0 ▼a Movement disorders.
650 2 ▼a Ataxia.
700 1 ▼a Subramony, Sankara H.
700 1 ▼a Durr, Alexandria.
830 0 ▼a Handbook of clinical neurology ; ▼v 3rd ser., v. 103.
856 4 0 ▼3 ScienceDirect ▼u https://oca.korea.ac.kr/link.n2s?url=http://www.sciencedirect.com/science/book/9780444518927
945 ▼a KLPA
991 ▼a E-Book(소장)

소장정보

No. 소장처 청구기호 등록번호 도서상태 반납예정일 예약 서비스
No. 1 소장처 중앙도서관/e-Book 컬렉션/ 청구기호 CR 616.808 등록번호 E14002679 도서상태 대출불가(열람가능) 반납예정일 예약 서비스 M

컨텐츠정보

목차

Basic aspects. The cerebellum
structure and connections ; Physiology of clinical dysfunction of the cerebellum ; Oculomotor aspects of the hereditary cerebellar ataxias ; Magnetic resonance and nuclear medicine imaging studies in ataxic disease ; Neuropathology of degenerative ataxias ; Approach to ataxic diseases.
Acquired ataxias. Acquired ataxias, infectious and para-infectious ; Ataxia in patients with brain infarcts and hemorrhages ; Ataxia resulting from posterior fossa tumors of childhood and other mass lesions ; Nutritional cerebellar degeneration, with comments on its relationship to Wernicke disease and alcoholism ; Immune-mediated acquired ataxias ; Toxic agents causing cerebellar ataxias ; Paraneoplastic cerebellar degeneration.
Degenerative ataxias. Epidemiology and population genetics of degenerative ataxias ; Sporadic adult onset ataxia of unknown aetiology. Degenerative ataxias
Mitochondrial, autosomal recessive and x-linked. Overview of autosomal recessive ataxias ; Friedrich''s ataxia ; Ataxia with vitamin E deficiency and abetalipoproteinemia ; Ataxia-telangiectasia ; Autosomal recessive cerebellar ataxias with oculomotor apraxia ; Other autosomal recessive and childhood ataxias ; Ataxia in mitochondrial disorders ; Fragile X-associated tremor/ataxia syndrome.
Degenerative ataxias
autosomal dominant. Overview of autosomal dominant ataxias ; Spinocerebellar ataxia type 1, 2 ; Machado-Joseph disease/spinocerebellar ataxia type 3 ; Spinocerebellar ataxia type 5, 6, 7 ; Clinical and genetic features of spinocerebellar ataxia type 8 ; Spinocerebellar ataxia type 10, 11, 12, 13, 14, 15, 20, 25, 28 ; Other spinocerebellar ataxias ; Dentatorubral-pallidoluysian atrophy ; Episodic ataxias 1 and 2.
Other issues. Ataxias related to sensory neuropathies ; Frontal lobe ataxia ; Balance and gait problems in the elderly ; Treatment and management issues in ataxic disease.

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