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1. |
Message from the Editor |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 1-2
I. Bogousslavsky,
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ISSN:0014-3022
DOI:10.1159/000117395
出版商:S. Karger AG
年代:1997
数据来源: Karger
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2. |
Cervical Artery Dissections |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 3-12
Didier Leys,
Christian Lucas,
Marc Gobert,
Ghislaine Deklunder,
Jean-Pierre Pruvo,
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摘要:
Cervical artery dissection (CAD) accounts for up to one fifth of ischemic strokes occurring before 45 years. Their increasing recognition is probably due to an increased clinical awareness of this condition in patients with painful ischemic events. The internal carotid artery is the most commonly affected vessel. Cerebral ischemia is the most serious consequence of a CAD. It may be due to hemodynamic factors or emboli. The enlargement of the artery may lead to a direct compression of the lower cranial nerves. CAD typically occurs in young adults with a mean age of 40 years with a male:female ratio of 1.5. After exclusion of traumatic cases, the average annual incidence rate of CAD is 2.6 per 100,000, but the reported incidence figures in the literature are likely to be an underestimation of the incidence of CAD. A spontaneous dissection is assumed when no or only minor trauma preceded the onset. However, the differentiation between spontaneous and traumatic dissections is artificial because of a continuum between both forms. The pathogenesis of dissections remains unknown in most cases. However, traumas and primary diseases of the arterial wall are the main predisposing factors. The clinical presentation of spontaneous dissections of the internal carotid artery includes cerebral ischemia, cervical or cranial pain, Homer’s syndrome and cranial nerve palsy; CAD may also be silent. Brainstem ischemic deficits and occipital pain are the most common findings in vertebral artery dissections, but these features may be biased because the most benign and the most severe cases may escape detection. The favorable natural history of CAD emphasizes the need for a noninvasive approach to the detection, monitoring and follow-up. This noninvasive approach can be obtained by means of CT scan, MRI, magnetic resonance angiography and ultrasonography, although angiography remains the gold standard for the diagnosis of arterial dissections. Follow-up studies suggest a fairly good overall prognosis in adults and in children. In many centers, CAD are treated by heparin at the acute stage, although the benefit of such a potentially dangerous treatment has never been proven by a randomized tria
ISSN:0014-3022
DOI:10.1159/000117396
出版商:S. Karger AG
年代:1997
数据来源: Karger
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3. |
Lähmungen der Sohlenmuskulatur bei Schußverletzungen des Nervus tibialis. |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 11-17
Franz Kramer, Prof. Dr.,
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ISSN:0014-3022
DOI:10.1159/000190982
出版商:S. Karger AG
年代:1915
数据来源: Karger
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4. |
Alcoholic Epilepsy: A Unified and Dynamic Classification |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 13-17
Fabrice Bartolomei,
Laurent Suchet,
Maryline Barrie,
Jean-Louis Gastaut,
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摘要:
The interactions between alcohol and the CNS are complex and there are experimental data suggesting that chronic and acute effects are different and often opposite. An intriguing hypothesis is that repeated alcohol withdrawal seizures (AWS) may render the brain more excitable, leading to an epileptog-enic state reminiscent of the ‘kindling’ model. To gain insight into this question we compared alcoholic patients with seizures related to episodes of AW (AWS) and patients with seizures unrelated to episodes of AW (UAWS). There were several significant differences between the AWS and UAWS groups. Age at admission for seizure was younger in the AWS groups (p < 0.005), seizure number was higher among patients with a history of seizures before admission in the UAWS group (p < 0.05). Neurologic signs were more frequent in the UAWS group (p < 0.05). Duration of intoxication was longer in the UAWS group and brain atrophy demonstrated by CT scan was more common in the UAWS group than the AWS group. Based on these findings, we propose a dynamic classification in which patients presenting seizures unrelated to any cause other than alcohol are classified in several successive stages of ‘alcoholic epilepsy’, the first being characterized by AWS and the last by persistent chronic s
ISSN:0014-3022
DOI:10.1159/000117397
出版商:S. Karger AG
年代:1997
数据来源: Karger
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5. |
Doppelseitige symmetrische Schläfen- und Parietallappenherde als Ursache vollständiger dauernder Worttaubheit bei erhaltener Tonskala, verbunden mit taktiler und optischer Agnosie. |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 17-38
K. Bonhoeffer, Prof. Dr.,
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ISSN:0014-3022
DOI:10.1159/000190983
出版商:S. Karger AG
年代:1915
数据来源: Karger
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6. |
Cerebral Oxygen Metabolism in Patients with Progressive Supranuclear Palsy: A Positron Emission Tomography Study |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 18-22
P. Santens,
J. De Reuck,
L. Crevits,
D. Decoo,
I. Lemahieu,
K. Strijckmans,
P. Goethals,
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摘要:
To investigate cerebral oxygen metabolism in progressive supranuclear palsy (PSP), 5 patients with a clinical diagnosis of PSP and a variable degree of cognitive deficit were selected for positron emission tomography (PET) of the brain. In 4 of them, a significant decrease in oxygen metabolism was found in all cortical regions, without frontal accentuation. In the group as a whole, this decrease was even slightly more marked in parietal and temporal regions. These findings are not consistent with earlier PET studies that demonstrated frontal targeting of hypometabolism in PSP patients. Part of this discrepancy can be explained by differences in methodology, although the use of different clinical criteria and overlap of PSP with other neurodegenerative diseases must be taken into account. It is concluded that the absence of frontal hypometabolism on PET examination does not exclude the diagnosis of PSP.
ISSN:0014-3022
DOI:10.1159/000117398
出版商:S. Karger AG
年代:1997
数据来源: Karger
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7. |
Comparison of Immediate-Release and Controlled Release Carbidopa/Levodopa in Parkinson’s Disease |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 23-27
Gilbert Block,
Charles Liss,
Scott Reines,
Joseph Irr,
Donald Nibbelink,
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摘要:
Background: Motor response fluctuations and dyskinesias compromise long-term levodopa therapy in Parkinson’s disease. Variations in plasma levodopa levels contribute to adverse reactions associated with chronic therapy. Therefore, sustained-release levodopa preparations may be associated with less motor fluctuations and a better outcome. We conducted a large, 5-year, multicenter study to address this hypothesis. Methods: Six hundred and eighteen nonfluctuating patients with Parkinson’s disease never exposed to levodopa therapy were randomized to (Sinemet® CR 50/200) sustained-release or immediate-release (Sinemet® 25/100) carbidopa/levodopa preparations in 35 centers worldwide. Dosage titration occurred over the 5 years of evaluations to maintain an optimal response. The primary endpoint, the ‘event’, was the presence of motor fluctuations, as defined by 20% ‘off time or 10% ‘on’ time with dyskinesias as recorded in the patient diary, or greater than or equal to a 50% positive response on the physician fluctuations questionnaire. Clinical rating scales, Nottingham Health Profile (NHP) and adverse reactions were also recorded. Findings: During the 5 years of the study, both treatment groups responded extremely well to therapy. The incidence of all patients reaching the ‘event’ was low, approximately 20% by diary criteria and 16% by questionnaire definition, and there was no significant difference between the two treatment groups. Activities of daily living scores in the Unified Parkinson Disease Rating Scale (UPDRS) consistently favored the Sinemet CR treatment group and a number of the NHP scales also favored the CR group. Based upon the frequency of adverse experiences, and the overall low incidence of withdrawals, the two treatment groups demonstrated very similar safety profiles. The most common drug-related effect was nausea; seen in 20% of patients. Other drug-related effects were dizziness, insomnia, abdominal pain, dyskinesia, headache and depression. Drug-related withdrawals were less than 10% of all patients, primarily due to nervous/psychiatric complaints. Interpretation: During a 5-year treatment period, control of parkinsonian symptoms was maintained by both immediate-release and sustained-release carbidopa/levodopa. Both treatment regimens were associated with a low incidence of motor fluctuations and dyskinesias. There was a statistically significant difference (p < 0.05) in activities of daily living as measured by the UPDRS in
ISSN:0014-3022
DOI:10.1159/000117399
出版商:S. Karger AG
年代:1997
数据来源: Karger
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8. |
Aura Phenomena during Syncope |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 28-32
T. Benke,
M. Hochleitner,
G. Bauer,
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摘要:
We studied the frequency and clinical characteristics of aura phenomena in 60 patients with cardiac and 40 subjects with vasovagal syncopes. The majority (93%) of all syncope patients recalled having experienced an aura. Aura phenomena were similar in both groups and were mostly compound auras comprising epigastric, vertiginous, visual, or somatosensory experiences, but were more detailed in the noncardiac group. The localizing significance of auras preceding a syncope was generally poor. Although hard to distinguish from epileptic auras from their structure and shape, syncope-related auras lacked symptoms that are commonly reported after epileptic seizures such as tastes, smells, déjà vu phenomena, scenic visual perceptions, and speech impairments. A detailed anamnestic exploration of auras seems worthwile in unexplained disorders of consciousnes
ISSN:0014-3022
DOI:10.1159/000117400
出版商:S. Karger AG
年代:1997
数据来源: Karger
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9. |
Announcement |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 32-32
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PDF (128KB)
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ISSN:0014-3022
DOI:10.1159/000117401
出版商:S. Karger AG
年代:1997
数据来源: Karger
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10. |
Poor Outcome of Bilateral Congenital Choroid Plexus Papillomas with Extreme Hydrocephalus |
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European Neurology,
Volume 37,
Issue 1,
1915,
Page 33-37
Concezio Di Rocco,
Aldo Iannelli,
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摘要:
Bilateral choroid plexus papillomas, or villous hypertrophy of the choroid plexus, is a very rare entity that presents serious therapeutical problems in the management of secondary oversecretive hydrocephalus. The authors report the cases of 2 infants affected by this condition, and cured with removal of the lateral ventricle papillomas and with cerebrospinal fluid (CSF) ventriculoperi-toneal shunt insertions. In both cases the CSF shunting alone or the removal of only 1 papilloma did not suffice in controlling the intracranial hypertension. In both infants late outcome was unsatisfactory. The poor prognosis associated with bilateral choroid papillomas in the infants described in the present report may be explained by the precocious onset of the disease, diagnosed during fetal life, and by the marked cerebral alterations already apparent in the immediate postnatal period on the neuroradiological examinations. Repeated surgical procedures, which were necessary to control the associated hydrocephalus in these patients, might have also played a significant negative role.
ISSN:0014-3022
DOI:10.1159/000117402
出版商:S. Karger AG
年代:1997
数据来源: Karger
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