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Cardoso, Francisco and Goetz, Christopher G. and Mestre, Tiago A. and Sampaio, Cristina and Adler, Charles H. and Berg, Daniela and Bloem, Bastiaan R. and Burn, David J. and Fitts, Michael S. and Gasser, Thomas and Klein, Christine and de Tijssen, Marina A. J. and Lang, Anthony E. and Lim, Shen-Yang and Litvan, Irene and Meissner, Wassilios G. and Mollenhauer, Brit and Okubadejo, Njideka and Okun, Michael S. and Postuma, Ronald B. and Svenningsson, Per and Tan, Louis C. S. and Tsunemi, Taiji and Wahlstrom-Helgren, Sarah and Gershanik, Oscar S. and Fung, Victor S. C. and Trenkwalder, Claudia (2024) A Statement of the MDS on Biological Definition, Staging, and Classification of Parkinson's Disease. Movement Disorders, 39 (2). pp. 259-266. ISSN 0885-3185, DOI https://doi.org/10.1002/mds.29683.
Lim, Shen-Yang and Klein, Christine (2024) Parkinson's Disease is Predominantly a Genetic Disease. Journal of Parkinsons Disease, 14 (3). pp. 467-482. ISSN 1877-7171, DOI https://doi.org/10.3233/JPD-230376.
Closas, Alfand Marl F. Dy and Lohmann, Katja and Tan, Ai Huey and Ibrahim, Norlinah Mohamed and Lim, Jia Lun and Tay, Yi Wen and Muthusamy, Kalai Arasu and Ahmad Annuar, Azlina and Klein, Christine and Lim, Shen -Yang (2023) A KMT2B frameshift variant causing focal dystonia restricted to the oromandibular region after long-term follow-up. Journal of Movement Disorders, 16 (1). 91+. ISSN 2005-940X, DOI https://doi.org/10.14802/jmd.22109.
Lim, Jia Lun and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Ibrahim, Khairul Azmi and Aziz, Zariah Abdul and Mawardi, Ahmad Shahir and Puvanarajah, Santhi Datuk and Lim, Thien Thien and Looi, Irene and Ooi, Joshua Chin Ern and Chia, Yuen Kang and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine and Ahmad-Annuar, Azlina and Lim, Shen-Yang (2022) Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: Mutational spectrum and clinical features. Journal of Neural Transmission, 129 (1). pp. 37-48. ISSN 0300-9564, DOI https://doi.org/10.1007/s00702-021-02421-0.
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Lim, Kai Bin and Lit, Lei Cheng and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation. Neurology Asia, 26 (1). pp. 161-166. ISSN 1823-6138,
Lim, Shen-Yang and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Tay, Yi Wen and Lim, Jia Lun and Ramli, Norlisah and Teh, Pei Chiek and Kuppusamy, Rishikesan and Tan, Chong Tin and Goh, Khean Jin and Viswanathan, Shanthi and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2021) Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters. Neurology Asia, 26 (1). pp. 167-173. ISSN 1823-6138,
Lim, Shen-Yang and Lim, Jia Lun and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Lim, Kai Bin and Tay, Yi Wen and Shing, Yee Lee and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2020) Clinical phenotype of LRRK2R1441C in 2 Chinese sisters. Neurodegenerative Diseases, 20 (1). pp. 39-45. ISSN 1660-2854, DOI https://doi.org/10.1159/000508131.
Lim, Shen-Yang and Lim, Jia Lun and Ahmad-Annuar, Azlina and Lohmann, Katja and Tan, Ai Huey and Lim, Kai Bin and Tay, Yi Wen and Shing, Yee Lee and Muthusamy, Kalai Arasu and Bauer, Peter and Rolfs, Arndt and Klein, Christine (2020) Clinical phenotype ofLRRK2R1441C in 2 Chinese sisters. Neurodegenerative Diseases, 20 (1). pp. 39-45. ISSN 1660-2854, DOI https://doi.org/10.1159/000508131.
