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Titlebook: Oxidative Stress and Neuroprotection; H. Parvez,P. Riederer Book 2006 Springer-Verlag Vienna 2006 Alzheimer.Morbus Parkinson.Parkinson.alz

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樓主: Buchanan
11#
發(fā)表于 2025-3-23 12:28:55 | 只看該作者
PD-related psychosis: pathophysiology with therapeutical strategies, considered to represent major contributors to patient and caregiver distress and nursing home placement..Endogenous (related to the disease process itself) as well as exogenous (related to therapeutical interventions) psychotogenic factors may contribute to the development of psychotic symptoms in
12#
發(fā)表于 2025-3-23 14:01:28 | 只看該作者
13#
發(fā)表于 2025-3-23 18:52:28 | 只看該作者
14#
發(fā)表于 2025-3-23 22:21:55 | 只看該作者
,Molecular mechanism of the relation of monoamine oxidase B and its inhibitors to Parkinson’s diseasn and neuromelanin. MAO B inhibitors such as L-(?)-deprenyl (selegiline) and rasagiline are effective for the treatment of PD. Concerning the mechanism of the clinical efficacy of MAO B inhibitors in PD, the inhibition of DA degradation (a symptomatic effect) and also the prevention of the formation
15#
發(fā)表于 2025-3-24 02:52:23 | 只看該作者
16#
發(fā)表于 2025-3-24 08:02:37 | 只看該作者
17#
發(fā)表于 2025-3-24 13:58:25 | 只看該作者
,Isatin, an endogenous MAO inhibitor, and a rat model of Parkinson’s disease induced by the Japanesen, but not selegiline. These findings suggest that JEV-infected rats may serve as a model of Parkinson’s disease and that exogenously administered isatin and selegiline can improve JEV-induced parkinsonism by increasing DA concentrations in the striatum.
18#
發(fā)表于 2025-3-24 18:39:50 | 只看該作者
,Neuroprotection for Parkinson’s disease, clinical investigation can be increased. Recent years have seen the utilization of more sensitive study methods in PD neuroprotection research, such as staggered wash-in, 2 × 2 factorial, and “futility” trial designs. The results of several ongoing PD neuroprotection trials are planned for release
19#
發(fā)表于 2025-3-24 21:21:17 | 只看該作者
20#
發(fā)表于 2025-3-25 01:42:58 | 只看該作者
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