Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Ai-Huey Tan"'
Autor:
Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J. Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih-Hua Fang, Peter Heutink, Kishore R. Kumar, Shen-Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolo Mencacci, Katja Lohmann, Christine Klein, the Global Parkinson’s Genetic Program (GP2)
Publikováno v:
npj Parkinson's Disease, Vol 9, Iss 1, Pp 1-5 (2023)
Abstract The Monogenic Network of the Global Parkinson’s Genetics Program (GP2) aims to create an efficient infrastructure to accelerate the identification of novel genetic causes of Parkinson’s disease (PD) and to improve our understanding of al
Externí odkaz:
https://doaj.org/article/8b77c4b847d04eeb869510a018f48bee
Autor:
Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J. Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih-Hua Fang, Peter Heutink, Kishore R. Kumar, Shen-Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolo Mencacci, Katja Lohmann, Christine Klein, the Global Parkinson’s Genetic Program (GP2)
Publikováno v:
npj Parkinson's Disease, Vol 9, Iss 1, Pp 1-3 (2023)
Externí odkaz:
https://doaj.org/article/3f7a6c99f648490596d129df6135734f
Autor:
Kheng-Seang Lim, Ai-Huey Tan, Chun-Shen Lim, Kek-Heng Chua, Ping-Chin Lee, Norlisah Ramli, Giri Shan Rajahram, Fatimah Tina Hussin, Kum-Thong Wong, Meenakshi B Bhattacharjee, Ching-Ching Ng
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135470 (2015)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary stroke caused by mutations in NOTCH3 gene. We report the first case of CADASIL in an indigenous Rungus (Kadazan-Dusun) family in
Externí odkaz:
https://doaj.org/article/521a9a389a79420ba97959db651b1788
Autor:
Kheng-Seang Lim, Ai-Huey Tan, Chun-Shen Lim, Kek-Heng Chua, Ping-Chin Lee, Norlisah Ramli, Giri Shan Rajahram, Fatimah Tina Hussin, Kum-Thong Wong, Meenakshi B Bhattacharjee, Ching-Ching Ng
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0138600 (2015)
Externí odkaz:
https://doaj.org/article/6b956a3d8e164a05ba01814406871ea0
Publikováno v:
JGH Open, Vol 5, Iss 4, Pp 414-419 (2021)
Abstract The gut–brain axis is a hot topic in Parkinson's disease (PD). It has been postulated that gut pathogens and dysbiosis can contribute to peripheral inflammatory states or trigger downstream metabolic effects that exacerbate the neurodegene
Externí odkaz:
https://doaj.org/article/f327e53853444e82ad59a787250d998a
Autor:
Ai Huey Tan1,2 aihuey.tan@gmail.com, Su Lyn, Adeline3, Ramli, Norlisah Mohd4, Weng Khong Lim5,6, Peng Loon Cheah4, Jing Xian Teo5, Jyn Ling Kuan5,6, Yi Jayne Tan3, Jia Lun Lim1, Guo Yan Chew, Elaine7,8, Jia Nee Foo7,8, Khean Jin Goh1, Eng-King Tan3, Shen-Yang Lim1,2, AH Tan1, ASL Ng1
Publikováno v:
Neurology Asia. 2023, Vol. 28 Issue 1, p185-189. 8p.
Publikováno v:
Journal of Movement Disorders. 16:138-151
Patients with Parkinson’s disease (PD) face a multitude of gastrointestinal (GI) symptoms, including nausea, bloating, reduced bowel movements, and difficulties with defecation. These symptoms are common and may accumulate during the course of PD b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe5d379dbfc3a932ac2d22550576566
https://doi.org/10.14802/jmd.22220
https://doi.org/10.14802/jmd.22220
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
Publikováno v:
Nature Reviews Neurology. 18:476-495
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::937810a1997e01b13d1e1006311d51a4
https://doi.org/10.1038/s41582-022-00681-2
https://doi.org/10.1038/s41582-022-00681-2
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