Hereditary neuropathies and spinocerebellar atrophies: [64 tables]
Gespeichert in:
| Format: | Buch |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
Amsterdam [u.a.]
Elsevier Science Publ.
1991
|
| Schriftenreihe: | Handbook of clinical neurology
60 Handbook of clinical neurology Revised series ; 16 |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Literaturangaben |
| Beschreibung: | XVIII, 850 S. zahlr. Ill., graph. Darst. |
| ISBN: | 0444812792 |
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| 245 | 1 | 0 | |a Hereditary neuropathies and spinocerebellar atrophies |b [64 tables] |c this vol. has been co-ed. by J. M. B. Vianney de Jong |
| 264 | 1 | |a Amsterdam [u.a.] |b Elsevier Science Publ. |c 1991 | |
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Datensatz im Suchindex
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| adam_text | 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 REVISED SERIES 16 ELSEVIER SCIENCE
PUBLISHERS * AMSTERDAM ELSEVIER SCIENCE PUBLISHING CO., INC. * NEW YORK
CONTENTS FOREWORD V LIST OF CONTRIBUTORS B VII HEREDITARY NEUROPATHIES
CHAPTER 1. THE WORLD FEDERATION OF NEUROLOGY CLASSIFICATION OF
HEREDITARY AND CONGENITAL NEUROPATHIES - J. M. B. V. DE JONG 1 CHAPTER
2. HEREDITARY SENSORY NEUROPATHY ~ R. A. OUVRIER AND J. G. MCLEOD 5
CHAPTER 3. FAMILIAL DYSAUTONOMIA - G. B. SOLITARE 23 CHAPTER 4.
HEREDITARY CRANIAL NERVE PALSY - G. W. BRUYN 39 CHAPTER 5. PROGRESSIVE
EXTERNAL OPHTHALMOPLEGIA - D. A. CHAD AND D. A. DRACHMAN 47 CHAPTER 6.
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - P. J. M. VAN
WENSEN 61 CHAPTER 7. HE RE DO FAMILIAL PLEXUS BRACHIALIS NEUROPATHY - P.
J. M. VAN WENSEN 71 CHAPTER 8. GIANT AXONAL NEUROPATHY - J. LYCKLAMA A
NIJEHOLT 75 CHAPTER 9. FAMILIAL AMYLOID POLYNEUROPATHIES - H. STAUNTON
89 CHAPTER 10. NEUROPATHY OF PORPHYRIA - M. GREER 117 XVI CONTENTS
CHAPTER 11. METACHROMATIC LEUKODYSTROPHY - J. A. F. M. LUIJTEN 123
CHAPTER 12. NEUROPATHY IN BASSEN-KORNZWEIG DISEASE AND TANGIER DISEASE -
G. W. BRUYN 131 CHAPTER 13. THE NEUROPATHY OF FAMILIAL AMYOTROPHIC
CHOREA WITH ACANTHOCYTOSIS ( LEVINE-CRITCHLEY SYNDROME) - E. P. BHARUCHA
139 CHAPTER 14. NIEMANN-PICK DISEASE TYPES A, C AND D, GAUCHER DISEASE
TYPES I, II AND HI, AND WOLMAN DISEASE - S. C. PATEL, N. W. BARTON AND
C. ARGOFF 147 CHAPTER 15. RARE NEUROLIPIDOTIC POLYNEUROPATHIES - G. W.
BRUYN 165 CHAPTER 16. HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I
AND II (CHARCOT-MARIE-TOOTH DISEASE) - J. E. HOOGENDIJK AND M. DEVISSER
185 CHAPTER 17. DEJERINE-SOTTAS HYPERTROPHIC NEUROPATHY (HMSN TYPE HI)
AND ROUSSY-LEVY SYNDROME - W. SCHADY AND R. G. LASCELLES 213 CHAPTER 18.
HEREDOPATHIA ATACTICA POLYNEURITIFORMIS (PHYTANIC ACID STORAGE DISEASE;
REFSUM S DISEASE; HMSN TYPE IV) - O. H. SKJELDAL, O. STOKKE AND S.
REFSUM 225 CHAPTER 19. HEREDITARY MOTOR AND SENSORY NEUROPATHIES * RARE
VARIANTS - J. E. HOOGENDIJK AND J. M. B. V. DE JONG 243 CHAPTER 20.
CLINICAL WORK-UP OF THE PATIENT WITH A POLYNEUROPATHY - N. C. NOTERMANS,
J. H. J. WOKKE AND F. G. I. JENNEKENS 253 SPINOCEREBELLAR ATROPHIES
CHAPTER 21. THE CLASSIFICATION OF FAMILIAL ATAXIAS - S. H. SUBRAMONY AND
R. D. CURRIER 271 CHAPTER 22. HEREDITARY CONGENITAL CEREBELLAR ATROPHY ~
G. W. BRUYN 285 CHAPTER 23. FRIEDREICH S DISEASE - B. V. MANYAM 299
CHAPTER 24. NEUROLOGICAL ASPECTS OF XERODERMA PIGMENTOSUM (DE
SANCTIS-CACCHIONE SYNDROME) - E. BYRNE 335 CONTENTS CHAPTER 25.
CEREBELLOLENTAL DEGENERATION (MARINESCO-SJOGREN - SYNDROME) - M. COOK
AND E. BYRNE 341 CHAPTER 26. ATAXIA-TELANGIECTASIA - R. P. SEDGWICK AND
E. BODER 347 CHAPTER 27. MOLECULAR GENETICS OF ATAXIA-TELANGIECTASIA -
R. A. GATTI 425 CHAPTER 28. HEREDITARY PERIODIC ATAXIAS - S. L. MOON AND
W. C. KOLLER 433 CHAPTER 29. HEREDITARY POSTERIOR COLUMN ATAXIA - J. M.
B. V. DE JONG 445 CHAPTER 30. RECESSIVE SPASTIC ATAXIA OF
CHARLEVOIX-SAGUENAY ~ J.-P. BOUCHARD 451 CHAPTER 31. HEREDITARY SPASTIC
ATAXIA - M. J. EADIE 461 CHAPTER 32. JOSEPH DISEASE: AN AUTOSOMAL
DOMINANT MOTOR SYSTEM DEGENERATION - R. N. ROSENBERG 467 CHAPTER 33.
SCHUT FAMILY ATAXIA - L. J. SCHUT 481 CHAPTER 34. AUTOSOMAL DOMINANT
CEREBELLAR ATAXIA WITH SLOW SACCADES AND PERIPHERAL NEUROPATHY * A
VARIETY OF OLIVOPONTOCEREBELLAR DEGENERATION (WADIA TYPE) - N. H. WADIA
491 CHAPTER 35. OLIVOPONTOCEREBELLAR ATROPHY AND RETINAL DEGENERATION -
P. T. V. M. DE JONG AND V. P. T. HOPPENREIJS 505 CHAPTER 36.
OLIVOPONTOCEREBELLAR ATROPHY (DEJERINE-THOMAS TYPE) - M.J. EADIE 511
CHAPTER 37. NON-FAMILIAL OLIVOPONTOCEREBELLAR ATROPHY - A. STAAL AND J.
M. B. V. DE JONG 519 CHAPTER 38. STRIATONIGRAL DEGENERATION: ENTITY OR
NON-ENTITY? - G. W. BRUYN AND R. P. M. BRUYN 537 CHAPTER 39.
OLIVOPONTOCEREBELLAR ATROPHY WITH GLUTAMATE DEHYDROGENASE DEFICIENCY -
A. PLAITAKIS 551 CHAPTER 40. CEREBELLO-OLIVARY ATROPHY - M. J. EADIE 569
CHAPTER 41. ATAXIA WITH HYPOGONADISM (MATTHEWS-RUNDLE) - D. A. HOWELL
575 CONTENTS CHAPTER 42. LATE HEREDITARY AND ACQUIRED CEREBELLAR ATROPHY
- E. L. MANCALL 581 CHAPTER 43. DYSSYNERGIA CEREBELLARIS MYOCLONICA - G.
J. GILBERT 593 CHAPTER 44. DENTATO-RUBRO-PALLIDO-LUYSIAN ATROPHY - R.
IIZUKA AND K. HIRAYAMA 607 CHAPTER 45. GERSTMANN-STRAUSSLER-SCHEINKER
DISEASE - M. R. FARLOW, F. TAGLIAVINI, O. BUGIANI AND B. GHETTI 619
CHAPTER 46. X-LINKED RECESSIVE ATAXIA - G. W. BRUYN AND J. M. B. V. DE
JONG 635 CHAPTER 47. DIFFERENTIAL DIAGNOSIS OF THE PATIENT WITH
HEREDITARY CEREBELLAR AND SPINOCEREBELLAR DISORDERS - J. M. B. V. DE
JONG, P. A. BOLHUIS AND P. G. BARTH 643 CHAPTER 48. THALAMIC
DEGENERATIONS - J.-J. MARTIN 701 CHAPTER 49. PIGMENTARY RETINOPATHY
ASSOCIATED WITH NEUROLOGICAL DISEASE - P. T. V. M. DE JONG, G. W. BRUYN
AND J. M. B. V. DE JONG 717 CHAPTER 50. SYSTEMIC OPTICO-COCHLEO-DENTATE
DEGENERATION - P. CRAS AND J.-J. MARTIN 751 CHAPTER 51. HEREDITARY
PROGRESSIVE COCHLEOVESTIBULAR ATROPHY - B. A. YAQUB, S. M. ZAKZOUK, S.
M. AL-DEEB AND M. M.U. KABIRAJ 761 INDEX 781
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| indexdate | 2024-07-09T16:17:22Z |
| institution | BVB |
| isbn | 0444812792 |
| language | English |
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| physical | XVIII, 850 S. zahlr. Ill., graph. Darst. |
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| series | Handbook of clinical neurology |
| series2 | Handbook of clinical neurology Handbook of clinical neurology : Revised series |
| spelling | Hereditary neuropathies and spinocerebellar atrophies [64 tables] this vol. has been co-ed. by J. M. B. Vianney de Jong Amsterdam [u.a.] Elsevier Science Publ. 1991 XVIII, 850 S. zahlr. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Handbook of clinical neurology 60 Handbook of clinical neurology : Revised series 16 Literaturangaben Ataxie Neurogénétique Système nerveux - Maladies - Aspect génétique Ataxia Nervous system Diseases Genetic aspects Neurogenetics Spinocerebellar Degenerations Nervensystem (DE-588)4041643-4 gnd rswk-swf Neuralgie (DE-588)4198767-6 gnd rswk-swf Hirnatrophie (DE-588)4159929-9 gnd rswk-swf Neurogene Muskelatrophie (DE-588)4211660-0 gnd rswk-swf Erbkrankheit (DE-588)4015106-2 gnd rswk-swf Neurogene Muskelatrophie (DE-588)4211660-0 s DE-604 Nervensystem (DE-588)4041643-4 s Erbkrankheit (DE-588)4015106-2 s Hirnatrophie (DE-588)4159929-9 s Neuralgie (DE-588)4198767-6 s Jong, J. M. B. V. de Sonstige oth Handbook of clinical neurology 60 (DE-604)BV000069154 60 Handbook of clinical neurology Revised series ; 16 (DE-604)BV000015021 16 HEBIS Datenaustausch Mainz application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=002933338&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Hereditary neuropathies and spinocerebellar atrophies [64 tables] Handbook of clinical neurology Ataxie Neurogénétique Système nerveux - Maladies - Aspect génétique Ataxia Nervous system Diseases Genetic aspects Neurogenetics Spinocerebellar Degenerations Nervensystem (DE-588)4041643-4 gnd Neuralgie (DE-588)4198767-6 gnd Hirnatrophie (DE-588)4159929-9 gnd Neurogene Muskelatrophie (DE-588)4211660-0 gnd Erbkrankheit (DE-588)4015106-2 gnd |
| subject_GND | (DE-588)4041643-4 (DE-588)4198767-6 (DE-588)4159929-9 (DE-588)4211660-0 (DE-588)4015106-2 |
| title | Hereditary neuropathies and spinocerebellar atrophies [64 tables] |
| title_auth | Hereditary neuropathies and spinocerebellar atrophies [64 tables] |
| title_exact_search | Hereditary neuropathies and spinocerebellar atrophies [64 tables] |
| title_full | Hereditary neuropathies and spinocerebellar atrophies [64 tables] this vol. has been co-ed. by J. M. B. Vianney de Jong |
| title_fullStr | Hereditary neuropathies and spinocerebellar atrophies [64 tables] this vol. has been co-ed. by J. M. B. Vianney de Jong |
| title_full_unstemmed | Hereditary neuropathies and spinocerebellar atrophies [64 tables] this vol. has been co-ed. by J. M. B. Vianney de Jong |
| title_short | Hereditary neuropathies and spinocerebellar atrophies |
| title_sort | hereditary neuropathies and spinocerebellar atrophies 64 tables |
| title_sub | [64 tables] |
| topic | Ataxie Neurogénétique Système nerveux - Maladies - Aspect génétique Ataxia Nervous system Diseases Genetic aspects Neurogenetics Spinocerebellar Degenerations Nervensystem (DE-588)4041643-4 gnd Neuralgie (DE-588)4198767-6 gnd Hirnatrophie (DE-588)4159929-9 gnd Neurogene Muskelatrophie (DE-588)4211660-0 gnd Erbkrankheit (DE-588)4015106-2 gnd |
| topic_facet | Ataxie Neurogénétique Système nerveux - Maladies - Aspect génétique Ataxia Nervous system Diseases Genetic aspects Neurogenetics Spinocerebellar Degenerations Nervensystem Neuralgie Hirnatrophie Neurogene Muskelatrophie Erbkrankheit |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=002933338&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| volume_link | (DE-604)BV000069154 (DE-604)BV000015021 |
| work_keys_str_mv | AT jongjmbvde hereditaryneuropathiesandspinocerebellaratrophies64tables |