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  • Katerina Venderová, Ghassan Kabbach, +12 authors David S. Park
  • Medicine, Biology
  • Human molecular genetics
  • 2009 (First Published: 15 November 2009)
  • Mutations in the LRRK2 gene are the most common genetic cause of familial Parkinson's disease (PD). However, its physiological and pathological functions are unknown. Therefore, we generated severalContinue Reading
  • Ana Cabranes, Katerina Venderová, Eva de Lago, Filomena Fezza, Javier Fernández-ruiz
  • Biology, Medicine
  • Neurobiology of Disease
  • 2005 (First Published: 1 November 2005)
  • Recent studies have addressed the changes in endocannabinoid ligands and receptors that occur in multiple sclerosis, as a way to explain the efficacy of cannabinoid compounds to alleviate spasticity,Continue Reading