Analysis of LINGO1 (rs9652490) polymorphism in sporadic Parkinson's disease in a Polish population, and a meta-analysis

بواسطة Białecka M., Kurzawski M., Tan E.-K., Drozdzik M.
منشور في 2018

Analysis of LRRK2 G2019S and I2020T mutations in Parkinson's disease

بواسطة Bialecka M., Hui S., Klodowska-Duda G., Opala G., Tan E.-K., Drozdzik M.
منشور في 2018

Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk

بواسطة Bialecka M., Kurzawski M., Klodowska-Duda G., Opala G., Tan E.-K., Drozdzik M.
منشور في 2018

The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinsons disease, levodopa treatment response, and complications

بواسطة Bialecka M., Kurzawski M., Klodowska-Duda G., Opala G., Tan E.-K., Drozdzik M.
منشور في 2018

CARD15 variants in patients with sporadic Parkinson's disease

بواسطة Bialecka M., Kurzawski M., Klodowska-Duda G., Opala G., Juzwiak S., Kurzawski G., Tan E.-K., Drozdzik M.
منشور في 2018

Analysis of MDR1 haplotypes in Parkinson's disease in a white population

بواسطة Tan, E.-K., Drozdzik, M., Bialecka, M., Honczarenko, K., Klodowska-Duda, G., Teo, Y.Y., Tang, K., Wong, L.-P., Chong, S.S., Tan, C., Yew, K., Zhao, Y., Lee, C.G.L.
منشور في 2014