Literature DB >> 11199817

Workshop II: "neuroprotection"--the Lugano consensus.

P Riederer1, T Brücke, C Buhmann, T Müller, A Schwartz, A Storch, B Winner.   

Abstract

Consensus could be reached that there is overwhelming evidence of preclinical neuroprotection. However, the evidence of neuroprotection/neurorescue under clinical conditions is limited. Lessons from clinical trials designed to show neuroprotection (selegiline, amantadine, dopamine agonists) demonstrate that with the drugs available neuroprotection/neurorescue has to start as early as possible. A PET-controlled clinical trial with ropinirole shows that there seems to be a good chance for neuroprotection in the early phase of Parkinson's disease in patients treated from the very beginning of the disease while there is no such benefit in patients with a late start of a neuroprotective therapeutic strategy. Also long-term neuroprotection cannot be reached. Complicating factors to demonstrate clinical neuroprotection are discussed.

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Year:  2000        PMID: 11199817     DOI: 10.1007/pl00007774

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  2 in total

1.  Open-label treatment with desvenlafaxine in postmenopausal women with major depressive disorder not responding to acute treatment with desvenlafaxine or escitalopram.

Authors:  Claudio N Soares; Michael E Thase; Anita Clayton; Christine J Guico-Pabia; Kristen Focht; Qin Jiang; Susan G Kornstein; Phillip T Ninan; Cecelia P Kane
Journal:  CNS Drugs       Date:  2011-03       Impact factor: 5.749

Review 2.  Dopamine transporter (DAT) imaging in Parkinson's disease and related disorders.

Authors:  Thomas Brücke; Christof Brücke
Journal:  J Neural Transm (Vienna)       Date:  2021-12-15       Impact factor: 3.850

  2 in total

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