Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Yi Jayne, Tan"'
Autor:
Yi Jayne Tan, Alisa C. W. Yong, Jia Nee Foo, Michelle M. Lian, Weng Khong Lim, Jacqueline Dominguez, Zhi Hui Fong, Kaavya Narasimhalu, Hui Jin Chiew, Kok Pin Ng, Simon K. S. Ting, Nagaendran Kandiah, Adeline S. L. Ng
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 4, Pp 568-578 (2023)
Abstract Objective Frontotemporal dementia (FTD) encompasses a spectrum of neurodegenerative disorders, including behavioural variant FTD (bvFTD), semantic variant primary progressive aphasia (svPPA) and non‐fluent variant PPA (nfvPPA). While a str
Externí odkaz:
https://doaj.org/article/7f489c93b3ec4a15afdbc836d867afa0
Autor:
Xiao Deng, Seyed Ehsan Saffari, Nan Liu, Bin Xiao, John Carson Allen, Samuel Yong Ern Ng, Nicole Chia, Yi Jayne Tan, Xinyi Choi, Dede Liana Heng, Yew-long Lo, Zheyu Xu, Kay-Yaw Tay, Wing-Lok Au, Adeline Ng, Eng-King Tan, Louis C. S. Tan
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-8 (2022)
Abstract The biological underpinnings of the PD clusters remain unknown as the existing PD clusters lacks biomarker characterization. We try to identify clinical subtypes of Parkinson Disease (PD) in an Asian cohort and characterize them by comparing
Externí odkaz:
https://doaj.org/article/04fe2024ec5a412e97b2222c6a02e77d
Autor:
Eng Tah Goh, Christine Lock, Audrey Jia Luan Tan, Bee Ling Tan, Sai Liang, Robin Pillay, Sumeet Kumar, Azlina Ahmad-Annuar, Vairavan Narayanan, Janell Kwok, Yi Jayne Tan, Adeline SL Ng, Eng King Tan, Zofia Czosnyka, Marek Czosnyka, John D. Pickard, Nicole C. Keong
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveNormal pressure hydrocephalus (NPH) is a neurological condition characterized by a clinical triad of gait disturbance, cognitive impairment, and urinary incontinence in conjunction with ventriculomegaly. Other neurodegenerative diseases, suc
Externí odkaz:
https://doaj.org/article/12003f6a789f4346a21ccebb7d3dacce
Autor:
Adeline Su Lyn Ng, Juan Wang, Kwun Kei Ng, Joanna Su Xian Chong, Xing Qian, Joseph Kai Wei Lim, Yi Jayne Tan, Alisa Cui Wen Yong, Russell Jude Chander, Shahul Hameed, Simon Kang Seng Ting, Nagaendran Kandiah, Juan Helen Zhou
Publikováno v:
Alzheimer’s Research & Therapy, Vol 13, Iss 1, Pp 1-16 (2021)
Abstract Background Alzheimer’s disease (AD) and behavioral variant frontotemporal dementia (bvFTD) cause distinct atrophy and functional disruptions within two major intrinsic brain networks, namely the default network and the salience network, re
Externí odkaz:
https://doaj.org/article/4d4cc932afde4537a28a9a7f12d1ea6d
Autor:
Adeline Su Lyn Ng, Yi Jayne Tan, Alisa Cui Wen Yong, Seyed Ehsan Saffari, Zhonghao Lu, Ebonne Yulin Ng, Samuel Yong Ern Ng, Nicole Shuang Yu Chia, Xinyi Choi, Dede Heng, Shermyn Neo, Zheyu Xu, Nicole Chwee Har Keong, Kay Yaw Tay, Wing Lok Au, Louis Chew Seng Tan, Eng-King Tan
Publikováno v:
Molecular Neurodegeneration, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background The main motor subtypes of Parkinson’s disease (PD) include tremor-dominant (TD) and postural instability gait disorder (PIGD), with varying disease course that warrant the development of biomarkers capable of predicting progres
Externí odkaz:
https://doaj.org/article/6726f7a3e61441c6af07683d1088d811
Autor:
Yi Jayne Tan, Isabel Siow, Seyed Ehsan Saffari, Simon K.S. Ting, Zeng Li, Nagaendran Kandiah, Louis C.S. Tan, Eng King Tan, Adeline S.L. Ng
Publikováno v:
Journal of Alzheimer's Disease. 92:573-580
Background: Suppressor of tumorgenicity 2 (ST2) is highly expressed in brain tissue and is a receptor for interleukin 33 (IL-33). ST2 exists in two forms, a transmembrane receptor (ST2L) and a soluble decoy receptor (sST2). IL-33 binds to ST2L, trigg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e0f71af531e609e883f18b4d23638c0
https://doi.org/10.3233/jad-221072
https://doi.org/10.3233/jad-221072
Autor:
Ai Huey Tan, Adeline Su Lyn Ng, Norlisah Mohd Ramli, Weng Khong Lim, Peng Loon Cheah, Jing Xian Teo, Jyn Ling Kuan, Yi Jayne Tan, Jia Lun Lim, Elaine Guo Yan Chew, Jia Nee Foo, Khean Jin Goh, Eng-King Tan, Shen-Yang Lim
Publikováno v:
Neurology Asia. 28:185-189
A significant proportion of adult-onset neurological disorders remain diagnostic odysseys despite extensive evaluation. Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity (HBSL) is an autosomal recessive disorder caused by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82805d91e618466d631a33cae55a1cc7
https://doi.org/10.54029/2023vkd
https://doi.org/10.54029/2023vkd
Autor:
Jacqueline Dominguez, Jeryl Tan Yu, Yi Jayne Tan, Arlene Ng, Ma Fe De Guzman, Boots Natividad, Ma Luisa Daroy, Jemellee Cano, Justine Yu, Michelle M. Lian, Li Zeng, Weng Khong Lim, Jia Nee Foo, Adeline S. L. Ng
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontotemporal Dementia (FTD) is a common cause of Young Onset Dementia and has diverse clinical manifestations involving behavior, executive function, language and motor function, including parkinsonism. Up to 50% of FTD patients report a positive f
Externí odkaz:
https://doaj.org/article/4afb50e68e1c44d0ae5e01ca165644ac
Autor:
Zhiyong Chen, Yi Jayne Tan, Michelle M. Lian, Moses Tandiono, Jia Nee Foo, Weng Khong Lim, Nagaendran Kandiah, Eng-King Tan, Adeline S. L. Ng
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Leukodystrophies are a diverse group of genetic disorders that selectively involve the white matter of the brain and are a frequent cause of young-onset cognitive impairment. Genetic diagnosis is challenging. Data on the utility of incorporating brai
Externí odkaz:
https://doaj.org/article/b9a4a51bf4ec409c9ba639daf29f93d2
Autor:
Zhiyong, Chen, Monica, Saini, Jasmine S, Koh, Kalpana, Prasad, Swee Hoon, Koh, Karine S S, Tay, Ming, Lee, Yi Jayne, Tan, Adeline S L, Ng, Stacey Kiat Hong, Tay, Kong Bing, Tan, Ankit, Tandon, Jeane M M, Tan, Josiah Y H, Chai
Publikováno v:
Journal of Neuromuscular Diseases. 10:91-106
Aim: We describe a cohort of five patients with limb-girdle muscular dystrophy (LGMD) 2G/LGMD-R7 in a South-east Asian cohort. Background: LGMD2G/LGMD-R7-telethonin-related is caused by mutations in the TCAP gene that encodes for telethonin. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40ff6ceedd6b09b9014b46e52ceb028
https://doi.org/10.3233/jnd-221517
https://doi.org/10.3233/jnd-221517