Khanh-Nhat Tran-Viet
Overview
Explore the profile of Khanh-Nhat Tran-Viet including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
649
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0
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Recent Articles
11.
Macgregor S, Hewitt A, Hysi P, Ruddle J, Medland S, Henders A, et al.
Hum Mol Genet
. 2010 Apr;
19(13):2716-24.
PMID: 20395239
Optic nerve assessment is important for many blinding diseases, with cup-to-disc ratio (CDR) assessments commonly used in both diagnosis and progression monitoring of glaucoma patients. Optic disc, cup, rim area...
12.
Ronan S, Tran-Viet K, Burner E, Metlapally R, Toth C, Young T
Arch Ophthalmol
. 2009 Nov;
127(11):1511-9.
PMID: 19901218
Objective: To report a 3-generation white family clinically diagnosed variably with Wagner, Stickler, and Jansen syndromes and screened for sequence variants in the COL2A1 and CSPG2 genes. Wagner syndrome is...
13.
Metlapally R, Li Y, Tran-Viet K, Abbott D, Czaja G, Malecaze F, et al.
Invest Ophthalmol Vis Sci
. 2009 Apr;
50(9):4080-6.
PMID: 19387081
Purpose: Collagen involvement in myopia development via scleral remodeling is well-known. Recently, COL1A1 and COL2A1 gene polymorphisms were reported to be associated with high-grade and common myopia, respectively. This study...
14.
White T, Lu T, Metlapally R, Katowitz J, Kherani F, Wang T, et al.
Mol Vis
. 2008 Dec;
14:2458-65.
PMID: 19112531
Purpose: Anophthalmia and microphthalmia (A/M) are rare congenital ocular malformations presenting with the absence of eye components or small eyes with or without structural abnormalities. A/M can be isolated or...
15.
Metlapally R, Li Y, Tran-Viet K, Bulusu A, White T, Ellis J, et al.
Mol Vis
. 2008 Mar;
14:387-93.
PMID: 18334955
Purpose: The membrane-type frizzled-related protein (MFRP) gene is selectively expressed in the retinal pigment epithelium and ciliary body, and mutations of this gene cause nanophthalmos. The MFRP gene may not...
16.
Beetz C, Schule R, Deconinck T, Tran-Viet K, Zhu H, Kremer B, et al.
Brain
. 2008 Mar;
131(Pt 4):1078-86.
PMID: 18321925
Mutations in the receptor expression enhancing protein 1 (REEP1) have recently been reported to cause autosomal dominant hereditary spastic paraplegia (HSP) type SPG31. In a large collaborative effort, we screened...
17.
Zuchner S, Wang G, Tran-Viet K, Nance M, Gaskell P, Vance J, et al.
Am J Hum Genet
. 2006 Jul;
79(2):365-9.
PMID: 16826527
Hereditary spastic paraplegia (HSP) comprises a group of clinically and genetically heterogeneous diseases that affect the upper motor neurons and their axonal projections. For the novel SPG31 locus on chromosome...