Yushin Tsai
Overview
Explore the profile of Yushin Tsai including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
158
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lin W, Chang K, Wang C, Chen S, Fan P, Weng W, et al.
Clin Chim Acta
. 2013 Mar;
421:34-40.
PMID: 23485646
Background: Dravet syndrome (DS) is a rare form of intractable epilepsy. Children with DS often start having seizures in infancy, and gradually develop other seizure types. Several studies have demonstrated...
2.
Lin W, Lin S, Wang C, Tsai Y, Chen C, Tsai F
Genet Mol Biol
. 2011 Jul;
34(2):201-4.
PMID: 21734816
Cleidocranial dysplasia (CCD) is an autosomal dominant human skeletal disorder comprising hypoplastic clavicles, wide cranial sutures, supernumerary teeth, short stature, and other skeletal abnormalities. It is known that mutations in...
3.
Wan L, Lin H, Tsai Y, Lee C, Tsai C, Tsai F, et al.
Retina
. 2010 Nov;
30(10):1595-600.
PMID: 21060270
Purpose: The purpose of this study was to investigate tumor necrosis factor-α gene polymorphisms in unrelated Taiwan Chinese patients with wet age-related macular degeneration (AMD) and controls. Methods: In this...
4.
Lin W, Chou I, Lee N, Wang C, Hwu W, Lin S, et al.
Clin Chem Lab Med
. 2010 Feb;
48(4):485-8.
PMID: 20184535
Background: Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is an autosomal dominant developmental disorder that includes an eyelid malformation associated with (type I) or without (type II) premature ovarian failure (POF)....
5.
Lin W, Wang C, Lai C, Tsai Y, Wu J, Chen C, et al.
Clin Chim Acta
. 2008 Nov;
401(1-2):33-6.
PMID: 19036343
Background: 3-Hydroxy-3-methylglutaryl CoA lyase deficiency (HL deficiency) is a rare autosomal recessive mitochondrial disease characterized by a deficiency in the enzyme 3-Hydroxy-3-methylglutaryl CoA lyase (HMGCL). Here, we report on novel...
6.
Lin J, Tsai Y, Wan L, Lin H, Tsai Y, Lee C, et al.
Retina
. 2008 Sep;
28(10):1416-20.
PMID: 18784628
Purpose: To investigate whether a polymorphism in the complement factor H gene determines the risk for the development of early age-related macular degeneration (AMD). Methods: In this retrospective case-control study,...
7.
Lin W, Lin S, Wang C, Hwu W, Chuang C, Lin S, et al.
Clin Chim Acta
. 2008 May;
394(1-2):89-93.
PMID: 18486607
Background: Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is an autosomal recessive lysosomal storage disease induced by a deficiency of the enzyme N-acetylgalactosamine-4-sulfatase (arylsulfatase B, ARSB). The deficiency of ARSB...
8.
Lin J, Wan L, Tsai Y, Lin H, Tsai Y, Lee C, et al.
Am J Ophthalmol
. 2008 Apr;
145(6):1045-1051.
PMID: 18378209
Purpose: To investigate vascular endothelial growth factor (VEGF) gene polymorphisms in unrelated Taiwan Chinese patients with late age-related macular degeneration (AMD) and controls. Design: Retrospective case-control study. Methods: We enrolled...
9.
Lin J, Wan L, Tsai Y, Lin H, Tsai Y, Lee C, et al.
Retina
. 2008 Feb;
28(2):309-13.
PMID: 18301036
Purpose: To investigate HTRA1 polymorphisms in unrelated Taiwan Chinese patients with age-related macular degeneration (AMD) and control subjects without AMD. Methods: A total of 95 unrelated Taiwan Chinese patients with...
10.
Tsai Y, Lin J, Wan L, Lin H, Tsai Y, Lee C, et al.
Invest Ophthalmol Vis Sci
. 2008 Feb;
49(2):693-8.
PMID: 18235016
Purpose: To investigate polymorphisms in a candidate gene of interleukin (IL) in unrelated Taiwan Chinese patients with late age-related macular degeneration (AMD) and control subjects without AMD. Methods: In this...