Skip navigation
中文
English
DSpace
CRIS
Home
Organizations
Researchers
Research Outputs
Explore by
Organizations
Researchers
Research Outputs
Academic & Publications
Help
中文
English
NTU Scholars
National Taiwan University
/
National Taiwan University Hospital
/
National Taiwan University Hospital Hsin-Chu Branch
/
NTU Hsin-Chu Hospital
/
Neurology-NTUHHC
KAI-HSIANG STANLEY CHEN
Network Lab
View Statistics
Email Alert
RSS Feed
Information
Publications
32
Project
Publications
(All)
All
Articles
Review
Others
Show/Hide filters
Author
5
kai-hsiang chen
3
ruey-meei wu
2
lin h.-i.
1
chen k.-h.;chin-hsien lin
1
chen k.-h.;lin p.-c.;chen y.-j.;yang b.-s.;chin-hsien lin
1
chen k.-h.;wu r.-m.;lin h.-i.;chun-hwei tai;lin c.-h.
1
chen m.-l.
1
chen y.-j.
1
chin-hsien lin;chen k.-h.;chen m.-l.;lin h.-i.;wu r.-m.
1
chun-hwei tai
.
next >
Subject
5
[sdgs]sdg3
1
aged; algorithm; article; automation; case report; disease severity assessment; essential tremor; female; finger; finger tremor; human; intermethod comparison; male; optical instrumentation; priority journal; quantitative analysis; accelerometry; algorithm; devices; essential tremor; feasibility study; pathophysiology; procedures; severity of illness index; signal processing; tremor; validation study; accelerometry; aged; algorithms; essential tremor; feasibility studies; female; fingers; humans; male; optical devices; severity of illness index; signal processing, computer-assisted; tremor
1
alanine; arginine; glutamine; synaptojanin; synaptojanin 1; unclassified drug; valine; phosphatase; phosphoinositide 5-phosphatase; adult; aged; allele; amino acid substitution; article; autosomal recessive inheritance; cognitive defect; comorbidity; controlled study; dementia; exon; family history; female; gene frequency; gene mutation; genetic variability; heterozygosity; homozygosity; human; intron; major clinical study; male; missense mutation; motor dysfunction; mutational analysis; parkinson disease; parkinsonism; pathogenesis; phenotype; priority journal; seizure; sequence analysis; single nucleotide polymorphism; synj1 gene; taiwanese; very elderly; apraxias; asian continental ancestry group; cogan syndrome; complication; genetic association study; genetic variation; genetics; middle aged; mutation; parkinson disease; recessive gene; taiwan; adult; aged; alleles; apraxias; asian continental ancestry group; cogan syndrome; dementia; exons; female; genes, recessive; genetic association studies; genetic variation; humans; male; middle aged; mutation; parkinson disease; phosphoric monoester hydrolases; seizures; taiwan
1
ceftriaxone; metronidazole; acvrl1 gene; adult; article; brain abscess; case report; clinical feature; congenital blood vessel malformation; differential diagnosis; dna extraction; eng gene; epistaxis; facial nerve paralysis; family history; female; fever; follow up; gene; gene amplification; gene duplication; gene mutation; gene sequence; headache; human; limb weakness; liver arteriovenous fistula; liver disease; medical history; neurologic examination; nuclear magnetic resonance imaging; polymerase chain reaction; priority journal; pulmonary arteriovenous fistula; recurrent disease; rendu osler weber disease; slurred speech; thorax radiography; treatment duration; treatment response
1
levodopa; risperidone; sertraline; affective psychosis; aged; akinesia; anxiety disorder; article; atxn2 gene; auditory hallucination; bradykinesia; brain atrophy; cag repeat; case report; cognitive defect; differential diagnosis; disease severity; dose response; family history; female; follow up; gene; gene function; genetic screening; human; low drug dose; major depression; male; muscle rigidity; nuclear magnetic resonance imaging; parkinsonism; persecutory delusion; phenotypic variation; polyneuropathy; priority journal; psychologic assessment; schizophrenia; shy drager syndrome; single photon emission computer tomography; spinocerebellar ataxia type 2; spinocerebellar degeneration; taiwan; treatment outcome; visual hallucination
1
vitamin d; vitamin d receptor; 5' untranslated region; adult; aged; article; controlled study; ethnic group; female; gene; gene frequency; gene function; genetic association; genetic variability; genotype; human; major clinical study; male; parkinson disease; pathophysiology; priority journal; protein interaction; single nucleotide polymorphism; taiwanese; vdr gene; very elderly; vitamin blood level; parkinson's disease; taiwan; vitamin d; vitamin d receptor gene; adult; aged; aged, 80 and over; asian continental ancestry group; case-control studies; cohort studies; female; genome-wide association study; humans; male; middle aged; parkinson disease; polymorphism, genetic; receptors, calcitriol; risk; taiwan; vitamin d
Date issued
5
2010 - 2019
By type
5
journal article
Fulltext
4
no fulltext
1
with fulltext
Close filters
Refined By:
Author:
chin-hsien lin
Results 1-5 of 5 (Search time: 0.009 seconds).
Issue Date
Title
Author(s)
Source
scopus
WOS
Fulltext/Archive link
1
2016
Development of method for quantifying essential tremor using a small optical device
KAI-HSIANG CHEN
; Lin P.-C.; Chen Y.-J.; Yang B.-S.; CHIN-HSIEN LIN
Journal of Neuroscience Methods
26
20
2
2015
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population
KAI-HSIANG CHEN
; RUEY-MEEI WU
; Lin H.-I.; CHUN-HWEI TAI
; CHIN-HSIEN LIN
Neurobiology of Aging
14
12
3
2014
Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population
CHIN-HSIEN LIN
; KAI-HSIANG CHEN
; Chen M.-L.; Lin H.-I.; RUEY-MEEI WU
Neurobiology of Aging
30
25
4
2013
Brain abscess as an initial presentation in a patient of hereditary haemorrhagic telangiectasia caused by a novel ENG mutation
KAI-HSIANG CHEN
; CHIN-HSIEN LIN
BMJ Case Reports
7
0
5
2012
Unusual association of diseases/symptoms: Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2
KAI-HSIANG CHEN
; CHIN-HSIEN LIN
; RUEY-MEEI WU
BMJ Case Reports
7
0
Claim Researcher Page
Login via ORCID to claim this profile:
ORCID Login
Contact via feedback form
If you want contact administrator site clicking the follow button