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Hereditary neuropathies and spinocerebellar atrophies

Hereditary neuropathies and spinocerebellar atrophies

자료유형
단행본
개인저자
Vinken, P. J. Bruyn, G. W. Klawans, Harold L. Jong, J. M. B. V. de.
서명 / 저자사항
Hereditary neuropathies and spinocerebellar atrophies / editors, Pierre J. Vinken, George W. Bruyn, Harold L. Klawans ; this volume has been co-edited by J.M.B. Vianney De Jong.
발행사항
Amsterdam ;   New York :   Elsevier Science,   c1991.  
형태사항
xviii, 850 p. : ill. ; 27 cm.
총서사항
Handbook of clinical neurology ;rev. ser. 16, v. 60
ISBN
0444812792
서지주기
Includes bibliographical references and index.
일반주제명
Nervous system -- Diseases -- Genetic aspects. Ataxia Neurogenetics. Spinocerebellar Degeneration.
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245 0 0 ▼a Hereditary neuropathies and spinocerebellar atrophies / ▼c editors, Pierre J. Vinken, George W. Bruyn, Harold L. Klawans ; this volume has been co-edited by J.M.B. Vianney De Jong.
260 ▼a Amsterdam ; ▼a New York : ▼b Elsevier Science, ▼c c1991.
300 ▼a xviii, 850 p. : ▼b ill. ; ▼c 27 cm.
490 1 ▼a Handbook of clinical neurology ; ▼v rev. ser. 16, v. 60
504 ▼a Includes bibliographical references and index.
650 0 ▼a Nervous system ▼x Diseases ▼x Genetic aspects.
650 0 ▼a Ataxia
650 0 ▼a Neurogenetics.
650 2 ▼a Spinocerebellar Degeneration.
700 1 ▼a Vinken, P. J.
700 1 ▼a Bruyn, G. W.
700 1 ▼a Klawans, Harold L.
700 1 ▼a Jong, J. M. B. V. de.
830 0 ▼a Handbook of clinical neurology ; ▼v v. 60.

소장정보

No. 소장처 청구기호 등록번호 도서상태 반납예정일 예약 서비스
No. 1 소장처 의학도서관/보존서고2/ 청구기호 616.808 H236v 60 등록번호 131048381 도서상태 대출가능 반납예정일 예약 서비스 B M

컨텐츠정보

목차

HEREDITARY NEUROPATHIES

1. The World Federation of Neurology Classification of hereditary and congenital neuropathies (J.M.B.V. de Jong). 2. Hereditary sensory neuropathy (R.A. Ouvrier and J.G. McLeod). 3. Familial dysautonomia (G.B. Solitare). 4. Hereditary cranial nerve palsy (G.W. Bruyn). 5. Progressive external ophthalmoplegia (D.A. Chad and D.A. Drachman). 6. Hereditary neuropathy with liability to pressure palsies (P.J.M. van Wensen). 7. Heredofamilial plexus brachialis neuropathy (P.J.M. van Wensen). 8. Giant axonal neuropathy (J. Lycklama a Nijeholt). 9. Familial amyloid polyneuropathies (H. Staunton). 10. Neuropathy of porphyria (M. Greer). 11. Metachromatic leukodystrophy (J.A.F.M. Luijten). 12. Neuropathy in Bassen-Kornzweig disease and Tangier disease (G.W. Bruyn). 13. The neuropathy of familial amyotrophic chorea with acanthocytosis () (E.P. Bharucha). 14. Niemann-Pick disease types A, C and D, Gaucher disease types I, II and III, and Wolman disease (S.C. Patel, N.W. Barton and C. Argoff). 15. Rare neurolipidotic polyneuropathies (G.W. Bruyn). 16. Hereditary motor and sensory neuropathy types I and II () (J.E. Hoogendijk and M. de Visser). 17. Dejerine-Sottas' hypertrophic neuropathy () and Roussy-Levy syndrome (W. Schady and R.G. Lascelles). 18. Heredopathia atactica polyneuritiformis. Phytanic acid storage disease () () (O.H. Skjeldal, O. Stokke and S. Refsum). 19. Hereditary motor and sensory neuropathies - rare variants (J.E. Hoogendijk and J.M.B.V. de Jong). 20. Clinical work-up of the patient with a polyneuropathy (N.C. Notermans, J.H.J. Wokke and F.G.I. Jennekens).

SPINOCEREBELLAR ATROPHIES

21. The classification of familial ataxias (S.H. Subramony and R.D. Currier). 22. Hereditary congenital cerebellar atrophy (G.W. Bruyn). 23. Friedreich's disease (B.V. Manyam). 24. Neurological aspects of xeroderma pigmentosum () (E. Byrne). 25. Cerebellolental degeneration () (M. Cook and E. Byrne). 26. Ataxia-telangiectasia (R.P. Segdwick and E. Boder). 27. Molecular genetics of ataxia-telangiectasia (R.A. Gatti). 28. Hereditary periodic ataxias (S.L. Moon and W.C. Koller). 29. Hereditary posterior column ataxia (J.M.B.V. de Jong). 30. Recessive spastic ataxia of Charlevoix-Saguenay (J.-P. Bouchard). 31. Hereditary spastic ataxia (M.J. Eadie). 32. Joseph disease: an autosomal dominant motor system degeneration (R.N Rosenberg). 33. Schut family ataxia (L.J. Schut). 34. Autosomal dominant cerebellar ataxia with slow saccades and peripheral neuropathy - a variety of olivopontocerebellar degeneration () (N.H. Wadia). 35. Olivo - ponto - cerebellar atrophy and retinal degeneration (P.T.V.M. de Jong and V.P.T. Hoppenreijs). 36. Olivopontocerebellar atrophy () (M.J. Eadie). 37. Non-familial olivopontocerebellar atrophy (A. Staal and J.M.B.V. de Jong). 38. Striatonigral degeneration: entity or non-entity? (G.W. Bruyn and J.M.B.V. de Jong). 39. Olivopontocerebellar atrophy with glutamate dehydrogenase deficiency (A. Plaitakis). 40. Cerebello-olivary atrophy (M.J. Eadie). 41. Ataxia with hypogonadism () (D.A. Howell). 42. Late hereditary and acquired cerebellar atrophy (E.L. Mancall). 43. Dyssynergia cerebellaris myoclonica (G.J. Gilbert). 44. Dentato-rubro-pallido-luysian atrophy (R. Iizuka and K. Hirayama). 45. Gerstmann-Straussler-Scheinker disease (M.R. Farlow, F. Tagliavini, O. Bugiani and B. Ghetti). 46. X-linked recessive ataxia (G.W. Bruyn and J.M.B.V. de Jong). 47. Differential diagnosis and work-up of the patient with hereditary spinocerebellar ataxia (J.M.B.V. de Jong and P.A. Bolhuis). 48. Thalamic degenerations (J.-J. Martin). 49. Retinitis pigmentosa associated with neurological disease (P.T.V.M. de Jong, G.W. Bruyn and J.M.B.V. de Jong). 50. Systemic optico-cochleo-dentate degeneration (P. Cras and J.J. Martin). 51. Hereditary progressive cochleovestibular atrophy (B.A. Yaqub, S.M. Zakzouk, S.M. Al-Deeb and M.U. Kabiraj).


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