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/vufind/Search/Results?lookfor=%22Tan%2C+Ai+Huey%22&type=Person&sort=year
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PubPharm (112)
1
Orthostatic hypotension in Parkinson's disease : Sit-to-stand vs. supine-to-stand protocol and clinical correlates
enthalten in:
Parkinsonism & related disorders
| 2024
von
Lim, K.
|
Lim, S.
|
Hor, J.
| +6
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2
Understanding monogenic Parkinson's disease at a global scale
enthalten in:
medRxiv : the preprint server for health sciences
| 2024
von
Junker, J.
|
Lange, L.
|
Vollstedt, E.
| +31
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3
Understanding monogenic Parkinson's disease at a global scale
enthalten in:
bioRxiv.org
| 2024
von
Junker, J.
|
Lange, L.
|
Vollstedt, E.
| +30
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4
Longitudinal Changes in the Retinal Nerve Fiber Layer Thickness in Amyotrophic Lateral Sclerosis and Parkinson's Disease : A Comparative Study
enthalten in:
Journal of clinical neurology (Seoul, Korea)
| 2024
von
Taufik, S.
|
Ramli, N.
|
Tan, A.
| +3
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5
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2024
von
Ojo, O.
|
Bandres-Ciga, S.
|
Makarious, M.
| +110
UpdateOf: medRxiv. 2023 Nov 09;:. - PMID 38076854
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6
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas : Barriers and Opportunities
enthalten in:
Movement disorders clinical practice
| 2024
von
Tan, A.
|
Cornejo-Olivas, M.
|
Okubadejo, N.
| +9
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7
Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry
enthalten in:
Journal of movement disorders
| 2024
von
Lim, S.
|
Tan, A.
|
Foo, J.
| +17
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8
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas : Barriers and Opportunities
enthalten in:
Movement Disorders Clinical Practice
| 2024
von
Tan, A.
|
Cornejo‐Olivas, M.
|
Okubadejo, N.
| +9
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9
Exome sequencing in Asian populations identifies rare deficient
SMPD1
alleles that increase risk of Parkinson’s disease
enthalten in:
bioRxiv.org
| 2023
von
Chew, E.
|
Liu, Z.
|
Li, Z.
| +45
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10
Author Correction : Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)
enthalten in:
NPJ Parkinson's disease
| 2023
von
Lange, L.
|
Avenali, M.
|
Ellis, M.
| +121
ErratumFor: NPJ Parkinsons Dis. 2023 Jun 27;9(1):100. - PMID 37369645
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Parkinsonism & related disorders
9
Journal of movement disorders
7
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59
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36
Research Support, Non-U.S. Gov't
24
Parkinson’s disease
16
Parkinson's disease
15
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8
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6
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570
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EC 2.7.11.1
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5
genetics
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Camptocormia
4
Caregiver burden
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Early-onset PD
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