Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Yi Wen Tay"'
Autor:
Alfand Marl F. Dy Closas, Katja Lohmann, Ai Huey Tan, Norlinah Mohamed Ibrahim, Jia Lun Lim, Yi Wen Tay, Kalai Arasu Muthusamy, Azlina Binti Ahmad-Annuar, Christine Klein, Shen-Yang Lim
Publikováno v:
Journal of Movement Disorders. 16:91-94
KMT2B-linked dystonia (DYT-KMT2B) is a childhood-onset dystonia syndrome typically beginning in the lower limbs and progressing caudocranially to affect the upper limbs with eventual prominent craniocervical involvement. Despite its recent recognitio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17d0501300a982ab0380799e7fb45c8
https://doi.org/10.14802/jmd.22109
https://doi.org/10.14802/jmd.22109
Autor:
Siaw Cheng Wong, Zhun Foo Tan, Yi-Wen Tay, Wan Chung Law, Azlina Ahmad-Annuar, Ai Huey Tan, Shen-Yang Lim
Publikováno v:
Neurology Asia. 27:515-520
We describe the clinical features of a Sarawakian man of Ibanese ethnicity with young-onset Parkinson’s disease (PD), who carried a very rare homozygous PRKN exon 7 duplication. Truncal dystonia was a prominent feature on presentation, in addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05f6ac79e3bbf2fb9ab96453a349058e
https://doi.org/10.54029/2022frs
https://doi.org/10.54029/2022frs
Autor:
Shen-Yang Lim, Alfand Marl F. Dy Closas, Ai Huey Tan, Jia Lun Lim, Yi Jayne Tan, Yuganthini Vijayanathan, Yi Wen Tay, Raihanah binti Abdul Khalid, Wai Keong Ng, Ruban Kanesalingam, Pablo Martinez-Martin, Jia Nee Foo, Weng Khong Lim, Adeline Su Lyn Ng, Eng-King Tan
BackgroundProgressive supranuclear palsy (PSP) is a rare, disabling, neurodegenerative disease. There are limited studies on the spectrum of PSP predominance-types and their clinico-demographic features among Asian patients. We prospectively characte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1e0b56adffba08845799f2eba3a314
https://doi.org/10.1101/2022.10.01.22280553
https://doi.org/10.1101/2022.10.01.22280553
Autor:
Yi Wen Tay, Ai Huey Tan, Jia Lun Lim, Katja Lohmann, Khairul Azmi Ibrahim, Zariah Abdul Aziz, Yen Theng Chin, Ahmad Shahir Mawardi, Thien Thien Lim, Irene Looi, Yuen Kang Chia, Joshua Chin Ern Ooi, Wee Kooi Cheah, Alfand Marl F. Dy Closas, Lei Cheng Lit, Jia Wei Hor, Tzi Shin Toh, Kalai Arasu Muthusamy, Peter Bauer, Volha Skrahin, Arndt Rolfs, Christine Klein, Azlina Ahmad-Annuar, Shen-Yang Lim
Publikováno v:
Parkinsonism & Related Disorders. 111:105399
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3364a090cbdd4fc9df3cb5274b9f3055
https://doi.org/10.1016/j.parkreldis.2023.105399
https://doi.org/10.1016/j.parkreldis.2023.105399
Publikováno v:
Parkinsonism & Related Disorders. 110:105276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce3d288864da69d5f4f11192840dcc62
https://doi.org/10.1016/j.parkreldis.2022.105276
https://doi.org/10.1016/j.parkreldis.2022.105276
Autor:
Ahmad Shahir Mawardi, Santhi Datuk Puvanarajah, Ai Huey Tan, Christine Klein, Yen Theng Chin, Khairul Azmi, Jia Lun Lim, Shen-Yang Lim, Zariah Abdul Aziz, Norlisah Ramli, Katja Lohmann, Azlina Ahmad-Annuar, Yi Wen Tay, Peter Bauer, Arndt Rolfs
Publikováno v:
Parkinsonism & Related Disorders. 79:34-39
Background An improved understanding of the genetic determinants of Parkinson's disease (PD) in underrepresented populations, and better characterization of genotype-phenotype correlations in monogenic PD, are needed. Scarce literature exists regardi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37c98167318fb3fa64c6c3f88f6aeaa9
https://doi.org/10.1016/j.parkreldis.2020.08.015
https://doi.org/10.1016/j.parkreldis.2020.08.015
Autor:
Arndt Rolfs, Kai Bin Lim, Yee Lee Shing, Kalai Arasu Muthusamy, Christine Klein, Peter Bauer, Shen-Yang Lim, Azlina Ahmad-Annuar, Katja Lohmann, Ai Huey Tan, Yi Wen Tay, Jia Lun Lim
Publikováno v:
Neurodegenerative Diseases. 20:39-45
Pathogenic and risk variants in the LRRK2 gene are among the main genetic contributors to Parkinson’s disease (PD) worldwide, and LRRK2-targeted therapies for patients with PARK-LRRK2are now entering clinical trials. However, in contrast to the LRR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fad1117e5fe35a0302bedac52dc116e5
https://doi.org/10.1159/000508131
https://doi.org/10.1159/000508131
Autor:
Peiyan Ho, Laurence Tan, Evon Yi Wen Tay, Hong Hui Lin, Lee Yen Lim, Min Jia Chua, James Alvin Low
Publikováno v:
American Journal of Hospice and Palliative Medicine®. :104990912211481
Little has been published on the meaning of food to palliative care patients with anorexia. Our study aims to investigate the meaning of food in palliative patients with anorexia. Fifteen patients with anorexia were recruited from the Palliative Care
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfe71f6627f7ff427afb15c20ea5d26d
https://doi.org/10.1177/10499091221148141
https://doi.org/10.1177/10499091221148141
Autor:
Kalai Arasu Muthusamy, Azlina Ahmad-Annuar, Christine Klein, Peter Bauer, Khairul Azmi Ibrahim, Yuen Kang Chia, Zariah Abdul Aziz, Yi Wen Tay, Joshua Chin Ern Ooi, Thien Thien Lim, Ai Huey Tan, Jia Lun Lim, Arndt Rolfs, Ahmad Shahir Mawardi, Irene Looi, Santhi Datuk Puvanarajah, Shen-Yang Lim, Katja Lohmann
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 129(1)
GBA variants are associated with increased risk and earlier onset of Parkinson’s disease (PD), and more rapid disease progression especially with “severe” variants typified by p.L483P. GBA mutation screening studies from South-East Asia, with >
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234c4d4ba9db57172f6279c920aee825
https://pubmed.ncbi.nlm.nih.gov/34779914
https://pubmed.ncbi.nlm.nih.gov/34779914
Autor:
Thien Thien Lim, Azlina Ahmad-Annuar, Soo Kun Lim, Wee Kooi Cheah, Yi Wen Tay, Tzi Shin Toh, Khairul Azmi Ibrahim, Ai Huey Tan, Yuganthini Vijayanathan, Irene Looi, Santhi Datuk Puvanarajah, Shanthi Viswanathan, Jia Lun Lim, Eng-King Tan, Gaik Bee Eow, Ebonne Yulin Ng, Aroma Agape Gopalai, Shen-Yang Lim, Zariah Abdul-Aziz, Ping Chong Bee
BackgroundGenome-wide association studies (GWAS) have shown that variants in the 3-methylcrotonyl-CoA carboxylase (MCCC1)/lysosome-associated membrane protein 3 (LAMP3) loci (rs10513789, rs12637471, rs12493050) reduce the risk of Parkinson’s diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf5333218397f35d1e757335d719311c
https://zenodo.org/record/4527827
https://zenodo.org/record/4527827