|1.||Erb, Michael: 2 articles (08/2011 - 12/2009)|
|2.||Meinen, Sarina: 2 articles (08/2011 - 12/2009)|
|3.||Rüegg, Markus A: 2 articles (08/2011 - 12/2009)|
|4.||Meier, Thomas: 2 articles (08/2011 - 12/2009)|
|5.||Waldmeier, P C: 2 articles (12/2000 - 10/2000)|
|6.||Cools, A R: 2 articles (08/2000 - 01/2000)|
|7.||Andringa, G: 2 articles (08/2000 - 01/2000)|
|8.||Huang, Shengdong: 1 article (10/2013)|
|9.||Sun, Haixiang: 1 article (10/2013)|
|10.||Sun, Jianxin: 1 article (10/2013)|
|1.||Parkinson Disease (Parkinson's Disease)
12/01/2006 - "The discrepancy between the preclinical promise of TCH346 and the clinical outcome could have arisen because of the use of laboratory models that do not accurately reflect the pathogenesis of Parkinson's disease, the doses of study drug used, insensitive clinical endpoints, and the patient population selected for study."
12/01/2006 - "TCH346 as a neuroprotective drug in Parkinson's disease: a double-blind, randomised, controlled trial."
12/01/2006 - "Our aim was to assess TCH346 as a neuroprotective drug in patients with Parkinson's disease. "
01/01/2003 - "However, CGP 3466 pretreatment does not ameliorate survival and function of the dopaminergic neurons after grafting into a rat model of Parkinson's disease."
12/01/2000 - "In conclusion, our results indicate that CGP 3466 is able to prevent death of dopaminergic cells in in vitro and in vivo models of Parkinson's disease. "
01/01/2013 - "Omigapil therapy (0.1 mg/kg) improved respiratory rate and decreased skeletal and respiratory muscle fibrosis in dy(2J) mice. "
01/01/2013 - "dy(2J) mice treated with 0.1 mg/kg/day omigapil showed decreased percent fibrosis in both gastrocnemius (p<0.03) and diaphragm (p<0.001) compared to vehicle, and in diaphragm (p<0.013) when compared to 1 mg/kg/day omigapil treated mice. "
01/01/2013 - "Omigapil treatment decreases fibrosis and improves respiratory rate in dy(2J) mouse model of congenital muscular dystrophy."
08/01/2011 - "By combining mini-agrin with either transgenic Bcl2 expression or oral omigapil application, we show that the ameliorating effect of mini-agrin, which acts by restoring the mechanical stability of muscle fibres and, thereby, reduces muscle fibre breakdown and concomitant fibrosis, is complemented by apoptosis inhibitors, which prevent the loss of muscle fibres. "
|4.||Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
|5.||Motor Neuron Disease (Primary Lateral Sclerosis)
|1.||1- Methyl- 4- phenyl- 1,2,3,6- tetrahydropyridine (MPTP)
|4.||Tyrosine 3-Monooxygenase (Tyrosine Hydroxylase)
|8.||salicylhydroxamic acid (SHAM)