Truong CK - Search Results

1

The β₂-adrenoceptor agonist bronchodilators terbutaline and orciprenaline are also weak α₁-adrenoceptor antagonists.

Khammy MM, Truong CKH, Wright CE, Angus JA. Khammy MM, et al. Among authors: truong ckh. Eur J Pharmacol. 2020 Sep 5;882:173304. doi: 10.1016/j.ejphar.2020.173304. Epub 2020 Jun 24. Eur J Pharmacol. 2020. PMID: 32592771

2

Chemical and microbiological risk assessment of urban river water quality in Vietnam.

Nguyen KT, Nguyen HM, Truong CK, Ahmed MB, Huang Y, Zhou JL. Nguyen KT, et al. Among authors: truong ck. Environ Geochem Health. 2019 Dec;41(6):2559-2575. doi: 10.1007/s10653-019-00302-w. Epub 2019 May 7. Environ Geochem Health. 2019. PMID: 31065920

3

Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis.

Hiniker A, Wong LJ, Berven S, Truong CK, Adesina AM, Margeta M. Hiniker A, et al. Among authors: truong ck. Acta Neuropathol Commun. 2014 Sep 16;2:137. doi: 10.1186/s40478-014-0137-3. Acta Neuropathol Commun. 2014. PMID: 25223649 Free PMC article.

4

Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.

Tang S, Wang J, Zhang VW, Li FY, Landsverk M, Cui H, Truong CK, Wang G, Chen LC, Graham B, Scaglia F, Schmitt ES, Craigen WJ, Wong LJ. Tang S, et al. Among authors: truong ck. Hum Mutat. 2013 Jun;34(6):882-93. doi: 10.1002/humu.22307. Epub 2013 Apr 2. Hum Mutat. 2013. PMID: 23463613

5

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders.

Cui H, Li F, Chen D, Wang G, Truong CK, Enns GM, Graham B, Milone M, Landsverk ML, Wang J, Zhang W, Wong LJ. Cui H, et al. Among authors: truong ck. Genet Med. 2013 May;15(5):388-94. doi: 10.1038/gim.2012.144. Epub 2013 Jan 3. Genet Med. 2013. PMID: 23288206 Free article.

6

Finding twinkle in the eyes of a 71-year-old lady: a case report and review of the genotypic and phenotypic spectrum of TWINKLE-related dominant disease.

Van Hove JL, Cunningham V, Rice C, Ringel SP, Zhang Q, Chou PC, Truong CK, Wong LJ. Van Hove JL, et al. Among authors: truong ck. Am J Med Genet A. 2009 May;149A(5):861-7. doi: 10.1002/ajmg.a.32731. Am J Med Genet A. 2009. PMID: 19353676 Review.

7

Alpers syndrome with prominent white matter changes.

Bao X, Wu Y, Wong LJ, Zhang Y, Xiong H, Chou PC, Truong CK, Jiang Y, Qin J, Yuan Y, Lin Q, Wu X. Bao X, et al. Among authors: truong ck. Brain Dev. 2008 Apr;30(4):295-300. doi: 10.1016/j.braindev.2007.08.009. Epub 2007 Oct 17. Brain Dev. 2008. PMID: 17923349

8

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.

Wong LJ, Brunetti-Pierri N, Zhang Q, Yazigi N, Bove KE, Dahms BB, Puchowicz MA, Gonzalez-Gomez I, Schmitt ES, Truong CK, Hoppel CL, Chou PC, Wang J, Baldwin EE, Adams D, Leslie N, Boles RG, Kerr DS, Craigen WJ. Wong LJ, et al. Among authors: truong ck. Hepatology. 2007 Oct;46(4):1218-27. doi: 10.1002/hep.21799. Hepatology. 2007. PMID: 17694548

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

8 results

Search Page