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1. |
In Memoriam: Harold L. Klawans, MD |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 625-625
Christopher G. Goetz,
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ISSN:0885-3185
DOI:10.1002/mds.870130402
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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2. |
Case ascertainment uncertainties in prevalence surveys of Parkinson's disease |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 626-632
Dallas W. Anderson,
Walter A. Rocca,
Maarten C. De Rijk,
Francesco Grigoletto,
Mario O. Melcon,
Monique M. B. Breteler,
Demetrius M. Maraganore,
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摘要:
AbstractUsing unpublished data from five completed prevalence surveys of Parkinson's disease (PD), we investigated case ascertainment uncertainties that potentially have a direct effect on prevalence. These uncertainties arise from the choice of diagnostic criteria, the choice of screening method, and the amount of information lost because of nonresponse. The surveys were conducted in Argentina, India, China, Italy, and the Netherlands. Our analyses consisted of simple comparisons of prevalence results, positive predictive values (a screening measure), and nonresponse percentages. We found that (a) prevalence comparisons between surveys have diminished value if the surveys used different diagnostic criteria for PD; (b) screening performance may be affected adversely if symptom questions are answered by one family member for the entire family living together rather than by each family member individually; and (c) nonresponse from refusal or unavailability does not necessarily lead to bias, but special caution may be appropriate with prevalence results pertaining to elderly women.
ISSN:0885-3185
DOI:10.1002/mds.870130403
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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3. |
Factor structure of the unified Parkinson's disease rating scale: Motor examination section |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 633-636
Glenn T. Stebbins,
Christopher G. Goetz,
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摘要:
AbstractThe Unified Parkinson's Disease Rating Scale (UPDRS) is widely used to asses Parkinson's disease (PD) disability but its metric properties have not been extensively studied. We investigated the factor structure and internal consistency of the Motor Examination section of the UPDRS in a sample of 294 consecutive patients with idiopathic PD who were assessed while in the “on” state. There was a high degree of internal consistency. Factor analysis revealed six clinically distinct factors, three bradykinesia measures (axial/gait, right and left), one rigidity measure, and two tremor measures (rest and postural). These factors accounted for 78% of the variance. Total Motor Examination scores and selected factors correlated well with other examiner‐determined global ratings of PD disability (Hoehn and Yahr stage and Schwab‐England Activities of Daily Living score). These results suggest that the Motor Examination section of the UPDRS provides a useful measure of PD function as well as severity measures of six clinical disability
ISSN:0885-3185
DOI:10.1002/mds.870130404
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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4. |
Effects of SIB‐1508Y, a novel neuronal nicotinic acetylcholine receptor agonist, on motor behavior in parkinsonian monkeys |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 637-642
Jay S. Schneider,
Anne Pope‐Coleman,
Maria Van Velson,
Frederique Menzaghi,
G. Kenneth Lloyd,
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摘要:
AbstractThe potential antiparkinsonian effects of the centrally acting, subtype‐selective neuronal nicotinic acetylcholine receptor agonist (S)‐(7‐)‐‐5‐ethynyl‐3‐(1‐methyl‐2‐pyrrolidinyl)‐pyridine (SIB‐1508Y) was assessed on motor symptoms and disability scale ratings in three monkeys previously made parkinsonian by chronic exposure to the dopaminergic neurotoxin 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP). Compared with levodopa (L‐dopa), SIB‐1508Y exerted only mild antiparkinsonian effects when administered alone. Emetic effects of this drug interfered with potential therapeutic effects at higher doses. However, when a low, ineffective dose of SIB‐1508Y was combined with low, ineffective doses ofL‐dopa, a significant clinical effect was observed. These data suggest that subtype‐selective nicotinic acetylcholine receptor agonists may hold promise as antiparkinsonian agents, and when administered in combination withL‐dopa may allow a reduction in the dose ofL‐dop
ISSN:0885-3185
DOI:10.1002/mds.870130405
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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5. |
A pilot evaluation of the tolerability, safety, and efficacy of tolcapone alone and in combination with oral selegiline in untreated Parkinson's disease patients |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 643-647
Robert A. Hauser,
Eric Molho,
Heidi Shale,
Simon Pedder,
Ernest E. Dorflinger,
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摘要:
AbstractTolcapone is a potent, reversible catechol‐O‐methyltransferase (COMT) inhibitor with both peripheral and central activity. It has been demonstrated to improve motor function and allow levodopa dose reductions in Parkinson's disease (PD) patients who are experiencing either a stable response or motor fluctuations while on levodopa/dopa decarboxylase inhibitor therapy. Because striatal dopamine is metabolized by COMT and monoamine oxidase (MAO), central COMT inhibition alone or in combination with MAO inhibition might provide symptomatic benefit for patients not receiving levodopa. We conducted a pilot study to evaluate the tolerability, safety, and efficacy of tolcapone alone and in combination with oral selegiline in early untreated PD patients. Patients were randomized to receive 200 mg tolcapone three times a day or placebo for the 8 weeks of the study. Open‐label oral selegiline (5 mg in the morning and midday) was administered to all patients during the second 4 weeks of the study. There was no difference between treatment groups according to the investigator's assessment of tolerability at week 4. Ninety‐five percent of tolcapone‐treated patients and 98% of placebo‐treated patients experienced excellent or good tolerability during the first 4 weeks (95% confidence interval [CI]: −10.3, 5.7; p = 0.57). A decrease in tolerability occurred in the tolcapone group during the second 4 weeks of the study following the addition of selegiline. The most commonly reported side effects were diarrhea (31% tolcapone, 7% placebo), nausea (21% tolcapone, 2% placebo), urine discoloration (12% tolcapone, 0% placebo), dizziness (12% tolcapone, 5% placebo), headaches (12% tolcapone, 10% placebo), and abdominal pain (10% tolcapone, 5% placebo). We did not identify symptomatic benefit associated with tolcapone alone or in combination with oral selegiline in this group of otherwise untreate
ISSN:0885-3185
DOI:10.1002/mds.870130406
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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6. |
Inhibition of levodopa effects by internal pallidal stimulation |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 648-652
Paul Krack,
Pierre Pollak,
Patricia Limousin,
Dominique Hoffmann,
Abdelhamid Benazzouz,
Alim‐Louis Benabid,
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摘要:
AbstractWe report three patients with bilateral GPi stimulation for stage 4 Parkinson's disease (PD) with severe levodopa‐induced dyskinesias (LID). In all three it was possible to completely inhibit LID using high‐stimulation parameters. Parallel to complete inhibition of LID, an inhibition of the anti‐akinetic effect of levodopa was observed, whereas, at the same time, rigidity was markedly improved. GPi stimulation is adaptable over time, and stimulation parameters have to be programmed according to off‐and on‐period motor symptoms. The main interest of stimulation is the possibility of finding a compromise between LID alleviation in on‐phase without loss of the beneficial motor effects and improvement in parkinsonism in off‐phase. In some patients, residual dyskinesias have to be accepted so as not to aggravate on‐period motor symptoms by a presumed overinhibition of basal
ISSN:0885-3185
DOI:10.1002/mds.870130407
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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7. |
Event‐Related desynchronization to contingent negative variation and Self‐Paced movement paradigms in Parkinson's disease |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 653-660
Giuseppe Magnani,
Marco Cursi,
Letizia Leocani,
Maria Antonietta Volonté,
Tiziana Locatelli,
Aldo Elia,
Giancarlo Comi,
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摘要:
AbstractThe event‐related desynchronization (ERD) to voluntary movemtnt is an indicator of cortical activation with a high time resolution and a specific spatial representation. We have evaluated 10 patients affected by Parkinson's disease (PD), free fromL‐dopa treatment for at least 12 hours, and 10 control subjects. Each subject underwent ERD examination during self‐paced movement (SPM) and during contingent negative variation (CNV) paradigms. ERD was measured as the percentage decrease of alpha band power and calculated for frequency bands of 1 Hz, ranging between 8 and 12 Hz. For group comparisons, the frequency showing the highest ERD was selected for each subject and for each side. In the control group. ERD in the CNV paradigm began over the contralateral centroparietal electrodes 1475 ms before movement onset of the right hand and 1375 ms for the left. In the SPM paradigm, ERD started over the contralateral central electrodes 2150 ms and 1775 ms before movement onset of the right and left hand, respectively. In the PD group, ERD started over the contralateral central areas 800 ms and 475 ms before movement onset of the right and left hand, respectively, for CNV paradigm and 1200 ms and 750 ms for the right and left hand, respectively, for SPM paradigm. Therefore, contralateral ERD began closer to movement onset in PD compared with the control group in both paradigms. ERD over the sensorimotor areas ipsilateral to the movement was not significantly different in PD compared with the control group. The finding of delayed contralateral ERD in PD is according to the view that functional cortical activation related to movement preparation is impaired in PD. The lack of group differences in the onset of ipsilateral ERD, which appears close to movement execution than contralateral ERD both in normal subjects and in PD, suggests that different mechanisms may be involved in generating ERD over the hemispheres ipsilateral and contralateral to the movement, and that only the latter are impaired
ISSN:0885-3185
DOI:10.1002/mds.870130408
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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8. |
Apomorphine enantiomers protect cultured pheochromocytoma (PC12) cells from oxidative stress induced by H2O2and 6‐Hydroxydopamine |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 661-667
Michael Gassen,
Aviva Gross,
Moussa B. H. Youdim,
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摘要:
AbstractA significant body of evidence has been provided to support the hypothesis that oxidant stress may be responsible for the degeneration of dopaminergic neurons in the substantia nigra pars compacta in Parkinson's disease. Apomorphine, a dopamine D1/D2‐receptor agonist in the clinical therapy of Parkinson's disease, has been found to be a potent antioxidant and to prevent free radical reaction in rat brain mitochondrial fraction. In this article we show that 1–10 µM of apomorphine protects rat pheochromocytoma (PC12) cells from the toxic effects of H2O2(0.6 mM) and the neurotoxin 6‐hydroxydopamine (150 µM). Neither of these effects were exhibited by ascorbic acid, desferal, lisuride, or bromocriptine. Although pergolide exhibited some protection of PC12 cells against H2O2toxicity, it was not as potent as apomorphine. In light of the present findings and the clinical reports that parkinsonian patients on long‐term apomorphine therapy stabilize clinically and can be weaned offL‐dopa, one may assume that apomorphine can exert a neuroprotective activity by way of its potent antioxidant
ISSN:0885-3185
DOI:10.1002/mds.870130409
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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9. |
Dysfunction of Ib (Autogenic) spinal inhibition in patients with progressive supranuclear palsy |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 668-672
Edward J. Fine,
Mark Hallett,
Irene Litvan,
Nancy Tresser,
David Katz,
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摘要:
AbstractWe compared the activity of Ib spinal interneurons in five patients with progressive supranuclear palsy (PSP) with six age‐matched control subjects. Stimulation of the medial gastrocnemius nerve at motor threshold intensity activated Ib afferents that in turn inhibit H reflexes from the soleus muscle. Maximum inhibition occurred at interstimulus intervals of 6 and 8 ms for both control subjects and PSP patients and was significantly greater in the PSP patients. Increased Ib activity of PSP patients may be caused by loss of inhibition of Ib interneurons through degeneration of the medullary reticulospinal pathway. The corticospinal pathways, unopposed by the medullary reticulospinal tract, may excessively activate Ib internuron
ISSN:0885-3185
DOI:10.1002/mds.870130410
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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10. |
Efaroxan, an alpha‐2 antagonist, in the treatment of progressive supranuclear palsy |
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Movement Disorders,
Volume 13,
Issue 4,
1998,
Page 673-676
Olivier Rascol,
Kasia Sieradzan,
Hélène Peyro‐Saint‐Paul,
Claire Thalamas,
Christine Brefel‐Courbon,
Jean Michel Senard,
Philippe Ladure,
Jean Louis Montastruc,
Andrew Lees,
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摘要:
AbstractWe have tested, in a prospective randomized, double‐blind, placebo‐controlled, crossover, 12‐week study, the effects of 2 mg efaroxan, a potent alpha‐2 antagonist, given three times per day to 14 patients with progressive supranuclear palsy. Efaroxan did not induce any significant change on any motor assessment criteria. The present data do not confirm the assumption that the blockade of alpha‐2 receptors might be a useful pharmacologic strategy to improve patients with progressive supranucl
ISSN:0885-3185
DOI:10.1002/mds.870130411
出版商:Wiley Subscription Services, Inc., A Wiley Company
年代:1998
数据来源: WILEY
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