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Titlebook: Advances in Research on Neurodegeneration; Volume 6 W. Poewe,G. Ransmayr Conference proceedings 1999 Springer-Verlag Wien 1999 Huntington‘s

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Multidimensional Feller Processes implies that we are likely to use combination therapies and have to try to treat patients early. The latter will be necessarily connected with the demand for a novel clinical attitude to the diagnosis of the disease.
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Neuroprotective effect of chronic inactivation of the subthalamic nucleus in a rat model of Parkinsra dopaminergic somata when carried out one week prior to 6-hydroxydopamine injection in the striatum. Nevertheless neurochemical results showed that this lesion did not antagonize the striatal 6-hydroxydopamine-induced dopamine depletion in the striatum 15 days after 6-hydroxydopamine injection.
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,Antiglutamate therapy of ALS — which is the next step?, implies that we are likely to use combination therapies and have to try to treat patients early. The latter will be necessarily connected with the demand for a novel clinical attitude to the diagnosis of the disease.
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,Antiglutamate therapies in Huntington’s disease,ydrochloride and Coenzyme Q10 in 340 patients with Huntington’s disease is described. This is the largest and longest multi-center trial in Huntington’s disease to address the glutamate- and mitochondrialmediated hypotheses of neurodegeneration.
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Striatal reconstruction by striatal grafts,ence to corroborate or refute this hypothesis, in comparison with a lessspecific mechanism (or mechanisms) of recovery, is considered, including anatomical, electrophysiological and neurochemical demonstrations of functional circuit reconstruction in the host brain by striatal tissue transplants.
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,Dopamine agonists: what is the place of the newer compounds in the treatment of Parkinson’s diseasehan bromocriptine in this indication, at the cost of very similar adverse effects..In de novo levodopa naive patients, pramipexole and ropinirole did significantly better than placebo in short-term (few months) follow-up trials, at the cost again of classical dopaminergic adverse effects. Ropinirole
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Apomorphine has a potent antiproliferative effect on Chinese hamster ovary cells, during incubation; CHO-K1 cells exposed to apomorphine for a period as short as 1 h and then allowed to grow for three days were significantly reduced in number with respect to untreated control cells. After four hours of exposition to apomorphine (10 μM) the antiproliferative effect was similar to
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Potent neuroprotective and antioxidant activity of apomorphine in MPTP and 6-hydroxydopamine inducetyrosine hydroxylase activity. It is suggested that the neuroprotective effect of (R)-apomorphine against MPTP neurotoxicity derives from its radical scavenging and MAO inhibitory actions and not from its agonistic activity, since the mechanism of MPTP dopaminergic neurotoxicity involves the generat
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