T H Vu
Overview
Explore the profile of T H Vu including associated specialties, affiliations and a list of published articles.
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Articles
74
Citations
4189
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0
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Recent Articles
1.
Vu T, Kwon M, Ahmed S, Gule-Monroe M, Chen M, Sun J, et al.
AJNR Am J Neuroradiol
. 2019 Oct;
40(11):1960-1964.
PMID: 31582388
The use of transoral sonography-guided fine-needle aspiration for intraoperative localization of retropharyngeal masses has been described by Fornage et al. The purpose of this study was to assess the accuracy...
2.
Brodowski L, Schroder-Heurich B, Hubel C, Vu T, von Kaisenberg C, von Versen-Hoynck F
Am J Physiol Cell Physiol
. 2019 Jun;
317(2):C348-C357.
PMID: 31166709
Maternal endothelial dysfunction is a cental feature of preeclampsia (PE), a hypertensive disorder of pregnancy. Factors in the maternal circulation are thought to contribute to this endothelial dysfunction. Although understudied,...
3.
Vu T, Schellingerhout D, Guha-Thakurta N, Sun J, Wei W, Kappadth S, et al.
AJNR Am J Neuroradiol
. 2018 Dec;
40(1):142-149.
PMID: 30523145
Background And Purpose: Minimally invasive parathyroid surgery relies critically on image guidance, but data comparing the efficacy of various imaging modalities are scarce. Our aim was to perform a blinded...
4.
Laurent G, Bernhard C, Dufort S, Jimenez Sanchez G, Bazzi R, Boschetti F, et al.
Nanoscale
. 2016 Jun;
8(23):12054-65.
PMID: 27244570
Many studies have been devoted to adapting the design of gold nanoparticles to efficiently exploit their promising capability to enhance the effects of radiotherapy. In particular, the addition of magnetic...
5.
Vu T, Jirtle R, Hoffman A
Cytogenet Genome Res
. 2006 Apr;
113(1-4):202-8.
PMID: 16575181
The epigenetic marks on the IGF2R gene that encodes a receptor responsible for IGF-II degradation consist of differentially methylated DNA in association with multiple modifications on the associated histones. We...
6.
Mancuso M, Salviati L, Sacconi S, Otaegui D, Camano P, Marina A, et al.
Neurology
. 2002 Oct;
59(8):1197-202.
PMID: 12391347
Background: The mitochondrial DNA (mtDNA) depletion syndrome (MDS) is an autosomal recessive disorder of early childhood characterized by decreased mtDNA copy number in affected tissues. Recently, MDS has been linked...
7.
Tanji K, Kunimatsu T, Vu T, Bonilla E
Semin Cell Dev Biol
. 2001 Dec;
12(6):429-39.
PMID: 11735377
Genetic defects affecting the mitochondrial respiratory chain comprise an important cause of encephalomyopathies. Considering the structural complexity of the respiratory chain, its dual genetic control, and the numerous nuclear genes...
8.
Hirano M, Marti R, Vila M, Tadesse S, Nishigaki Y, Nishino I, et al.
Semin Cell Dev Biol
. 2001 Dec;
12(6):417-27.
PMID: 11735376
Depletion and multiple deletions of mitochondrial DNA (mtDNA) have been associated with a growing number of autosomal diseases that have been classified as defects of intergenomic communication. MNGIE, an autosomal...
9.
Killian J, Nolan C, Wylie A, Li T, Vu T, Hoffman A, et al.
Hum Mol Genet
. 2001 Sep;
10(17):1721-8.
PMID: 11532981
M6P/IGF2R imprinting first appeared approximately 150 million years ago following the divergence of prototherian from therian mammals. Although M6P/IGF2R is clearly imprinted in opossums and rodents, its imprint status in...
10.
Vu T, Hays A, Tanji K, YOUNGER D, Gundersen G, Eastwood A, et al.
Neurology
. 2001 Jul;
57(1):149-52.
PMID: 11445649
A 61-year-old man with muscle aches and persistently elevated serum creatine kinase had aggregates of randomly oriented, rhomboidal or rectangular protein crystalline inclusions in the sarcoplasm of type II fibers....