Facial diplegia: cranial variant of Guillain-Barré syndrome?

Por Tan, E K, Lim, S H, Wong, M C, Chan, L L
Publicado em 1999

Depression, anxiety, and apathy in Parkinson's disease: insights from neuroimaging studies

Por Wen, M.‐C., Chan, L. L., Tan, L. C. S., Tan, E. K.
Publicado no Eur J Neurol (2016)

A young man with parkinsonism

Por Thant, Z S, Chan, L L, Lim, E, Wong, M C, Tan, E K
Publicado em 2002

Three-dimensional MR volumetric analysis of the posterior fossa CSF space in hemifacial spasm

Por Chan, L -L., Ng, K -M., Fook-Chong, S, Lo, Y -L., Tan, E -K.
Publicado em 2009

Neurodegeneration: Etiologies and New Therapies

Por Tan, E. K., Srivastava, Amit K., Arnold, W. David, Singh, Mahendra P., Zhang, Yiying
Publicado no Biomed Res Int (2015)

A variant in the HS1-BP3 gene is associated with familial essential tremor

Por Higgins, J.J., Lombardi, R.Q., Pucilowska, J., Jankovic, J., Tan, E.K., Rooney, J.P.
Publicado em 2005

Case control study of diffusion tensor imaging in Parkinson's disease

Por Chan, L‐L, Rumpel, H, Yap, K, Lee, E, Loo, H‐V, Ho, G‐L, Fook‐Chong, S, Yuen, Y, Tan, E‐K
Publicado em 2007

LINGO1 VARIANT INCREASES RISK OF FAMILIAL ESSENTIAL TREMOR

Por Tan, E -K., Teo, Y -Y., Prakash, K -M., Li, R, Lim, H -Q., Angeles, D, Tan, L -C., Au, W -L., Yih, Y, Zhao, Y
Publicado em 2009

Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus

Por Tan, E.-K., Kwok, H.-K., Tan, L.C., Zhao, W.-T., Prakash, K.M., Au, W.-L., Pavanni, R., Ng, Y.-Y., Satake, W., Zhao, Y., Toda, T., Liu, J.-J.
Publicado em 2010

LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population

Por Gopalai, Aroma Agape, Lim, Shen-Yang, Chua, Jing Yi, Tey, Shelisa, Lim, Thien Thien, Mohamed Ibrahim, Norlinah, Tan, Ai Huey, Eow, Gaik Bee, Abdul Aziz, Zariah, Puvanarajah, Santhi Datuk, Viswanathan, Shanthi, Looi, Irene, Lim, Soo Kun, Tan, Li Ping, Chong, Yip Boon, Tan, Chong Tin, Zhao, Yi, Tan, E. K., Ahmad-Annuar, Azlina
Publicado em 2014

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Por Haugarvoll, K., Rademakers, R., Kachergus, J.M., Nuytemans, K., Ross, O.A., Gibson, J.M., Tan, E.-K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P., De Deyn, P. Paul, Engelborghs, S., Pickut, B., Uitti, R.J., Foroud, T., Nichols, W.C., Hagenah, J., Klein, C., Samii, A., Zabetian, C.P., Bonifati, V., Van Broeckhoven, C., Farrer, M.J., Wszolek, Z.K.
Publicado em 2008

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson’s disease: analysis of a large multi-center study

Por Wang, L., Heckman, M.G., Aasly, J. O., Annesi, G., Bozi, M., Chung, S. J., Clarke, C., Crosiers, D., Eckstein, G., Garraux, G., Hadjigeorgiou, G. M., Hattori, N., Jeon, B., Kim, Y. J., Kubo, M., Lesage, S., Lin, J. J., Lynch, T., Lichtner, P., Mellick, G. D., Mok, V., Morrison, K. E., Quattrone, A., Satake, W., Silburn, P. A., Stefanis, L., Stockton, J. D., Tan, E. K., Toda, T., Brice, A., Van Broeckhoven, C., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Maraganore, D. M., Gasser, T., Kruger, R., Farrer, M. J., Ross, O. A., Sharma, M.
Publicado no Neurobiol Aging (2016)