|
1. |
Report to the members of the Movement Disorder Society |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 1-1
Stanley Fahn,
Preview
|
PDF (71KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040101
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
2. |
The Movement Disorder Society : Constitution and by‐laws |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 2-5
Preview
|
PDF (265KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040102
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
3. |
Viewpoints on the Ramsay Hunt syndrome. The Ramsay Hunt syndrome is a useful clinical entity |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 6-12
C. D. Marsden,
J. A. Obeso,
Preview
|
PDF (498KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040103
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
4. |
The Ramsay Hunt syndrome is no longer a useful diagnostic category |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 13-17
Frederick Andermann,
Samuel Berkovic,
Stirling Carpenter,
Eva Andermann,
Preview
|
PDF (347KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040104
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
5. |
Ramsay Hunt syndrome, Unverricht‐Lundborg disease, or what? |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 18-19
A. E. Harding,
Preview
|
PDF (129KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040105
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
6. |
Posttraumatic movement disorders: A review |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 20-36
William C. Koller,
George F. Wong,
Anthony Lang,
Preview
|
PDF (1317KB)
|
|
ISSN:0885-3185
DOI:10.1002/mds.870040106
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
7. |
Reduced glutamate decarboxylase activity in the subthalamic nucleus in patients with tardive dyskinesia |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 37-46
Ulf Andersson,
Jan‐Erik Hägström,
Edward D. Levin,
Ulf Bondesson,
Milan Valverius,
Lars M. Gunne,
Preview
|
PDF (615KB)
|
|
摘要:
AbstractGlutamate decarboxylase (GAD) activity was measured in the nuclei of the basal ganglia in patients with neuroleptic‐induced tardive dyskinesia (TD) and controls matched for age and premortem state. In five TD patients, who all had a sudden death, a significant decrease in GAD activity was found in the subthalamic nucleus (STN). The lowered GAD activity in the STN may represent a biochemical substrate for neuroleptic‐induced
ISSN:0885-3185
DOI:10.1002/mds.870040107
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
8. |
Off‐period belching due to a reversible disturbance of oesophageal motility in Parkinso's disease and its treatment with apomorphine |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 47-52
P. A. Kempster,
A. J. Lees,
P. Crichton,
J. P. Frankel,
P. Shorvon,
Preview
|
PDF (348KB)
|
|
摘要:
AbstractTwo L‐dopa‐treated patients with Parkinson's disease who developed distressing belching during “off” periods are reported. In each case, contrast cine radiography revealed disturbed oesophageal motility which disappeared after injection of the dopamine receptor agonist apomorphine. It is suggested that central dopaminergic abnormalities may be important in the aetiology of “off period
ISSN:0885-3185
DOI:10.1002/mds.870040108
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
9. |
The evolution and distribution of morphological changes in the nervous system of the common marmoset following the acute administration of 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 53-74
W. R. G. Gibb,
M. Terruli,
A. J. Lees,
P. Jenner,
C. D. Marsden,
Preview
|
PDF (1760KB)
|
|
摘要:
AbstractSix young adult marmosets received 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine in multiple doses (total 8–16 mg/kg over 2–13 days) sufficient to produce a parkinsonian syndrome and were killed up to 3.5 months later. Cellular changes were found in the substantia nigra, ventral tegmental area, and hypothalamus. The earliest histological abnormalities were axonal swellings in proximal parts of nigrostriatal axons. Subsequent changes in the substantia nigra were reduced Nissl staining, reduced cell volume, and aggregation and loss of melanin granules. Other effects were reduced nuclear and nucleolar volumes, depletion of cells, and hyperplasia of glial cells. Shrunken cytoplasm and nuclei stained uniformaly with eosin, and no cells showed cytoplasmic swellings or inclusions. These cellular alterations, with nuclear chages resembling karyolysis, do not occur in Parkinson's disease, which is characterised by Lewy body inclusions and signs of chromatolysis. The rapid appearance of axonal swellings, disruption of Nissl substance, and cell shrinkage suggest an insult to energy producing mechanisms. In this study, the absence of histological evidence of toxicity in the locus coeruleus and also in the substantia innominata and in serotonergic cell groups is unlike the more wide‐spread degenerative changes of Park
ISSN:0885-3185
DOI:10.1002/mds.870040109
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
10. |
The use of glutethimide for treatment of essential tremor |
|
Movement Disorders,
Volume 4,
Issue 1,
1989,
Page 75-80
Fletcher H. McDowell,
Preview
|
PDF (303KB)
|
|
摘要:
AbstractTwo patients with long‐standing intention tremor that was interfering with their ability to maintain employment were treated with glutethimide. In both patients, this agent successfully supressed tremor at doses of 1,000 mg and 4,000 mg per day. Glutethimide has been taken for as long as 14 years in one patient without evidence of side effect
ISSN:0885-3185
DOI:10.1002/mds.870040110
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1989
数据来源: WILEY
|
|