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Items: 1 to 50 of 250

1.

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.

Tester DJ, Wong LCH, Chanana P, Gray B, Jaye A, Evans JM, Evans M, Fleming P, Jeffrey I, Cohen M, Tfelt-Hansen J, Simpson MA, Behr ER, Ackerman MJ.

J Pediatr. 2018 Dec;203:423-428.e11. doi: 10.1016/j.jpeds.2018.08.011. Epub 2018 Sep 26.

PMID:
30268395
2.

FARS2 deficiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance.

Almannai M, Wang J, Dai H, El-Hattab AW, Faqeih EA, Saleh MA, Al Asmari A, Alwadei AH, Aljadhai YI, AlHashem A, Tabarki B, Lines MA, Grange DK, Benini R, Alsaman AS, Mahmoud A, Katsonis P, Lichtarge O, Wong LC.

Mol Genet Metab. 2018 Nov;125(3):281-291. doi: 10.1016/j.ymgme.2018.07.014. Epub 2018 Jul 29.

PMID:
30177229
3.

Freeing Chinese Abused Women From Stereotype: A Pretest-Posttest Comparison Study on Group Intervention in Refuge Centers.

Choi AWM, Chan PY, Lo RTF, Wong LCL, Wong JYH, Tang DHM.

J Evid Inf Soc Work. 2018 Nov-Dec;15(6):599-616. doi: 10.1080/23761407.2018.1509409. Epub 2018 Aug 24.

PMID:
30142306
4.

Noncardiac genetic predisposition in sudden infant death syndrome.

Gray B, Tester DJ, Wong LC, Chanana P, Jaye A, Evans JM, Baruteau AE, Evans M, Fleming P, Jeffrey I, Cohen M, Tfelt-Hansen J, Simpson MA, Ackerman MJ, Behr ER.

Genet Med. 2018 Aug 24. doi: 10.1038/s41436-018-0131-4. [Epub ahead of print]

PMID:
30139991
5.

Psoriasis and infection. A clinical practice narrative.

Rademaker M, Agnew K, Anagnostou N, Andrews M, Armour K, Baker C, Foley P, Gebauer K, Gupta M, Marshman G, Rubel D, Sullivan J, Wong LC.

Australas J Dermatol. 2018 Aug 5. doi: 10.1111/ajd.12895. [Epub ahead of print] Review.

PMID:
30079566
6.

The lysolipid transporter Mfsd2a regulates lipogenesis in the developing brain.

Chan JP, Wong BH, Chin CF, Galam DLA, Foo JC, Wong LC, Ghosh S, Wenk MR, Cazenave-Gassiot A, Silver DL.

PLoS Biol. 2018 Aug 3;16(8):e2006443. doi: 10.1371/journal.pbio.2006443. eCollection 2018 Aug.

7.

The etiology and prognosis of super-refractory convulsive status epilepticus in children.

Lu WY, Weng WC, Wong LC, Lee WT.

Epilepsy Behav. 2018 Sep;86:66-71. doi: 10.1016/j.yebeh.2018.06.029. Epub 2018 Jul 10.

PMID:
30006260
8.

The effect of pre-phototest sun exposure on minimal erythema dose and minimal melanogenic dose among skin phototypes III, IV and V.

Wong LC, Jamil A, Md Nor N.

Photodermatol Photoimmunol Photomed. 2018 Nov;34(6):400-404. doi: 10.1111/phpp.12410. Epub 2018 Jul 17.

PMID:
29953669
9.

Novel insights into the functional metabolic impact of an apparent de novo m.8993T>G variant in the MT-ATP6 gene associated with maternally inherited form of Leigh Syndrome.

Uittenbogaard M, Brantner CA, Fang Z, Wong LC, Gropman A, Chiaramello A.

Mol Genet Metab. 2018 May;124(1):71-81. doi: 10.1016/j.ymgme.2018.03.011. Epub 2018 Mar 27.

PMID:
29602698
10.

Induction chemotherapy for locally advanced nasopharyngeal carcinoma treated with concurrent chemoradiation: A systematic review and meta-analysis.

Tan TH, Soon YY, Cheo T, Ho F, Wong LC, Tey J, Tham IWK.

Radiother Oncol. 2018 Oct;129(1):10-17. doi: 10.1016/j.radonc.2018.02.027. Epub 2018 Mar 16.

PMID:
29555182
11.

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

Tester DJ, Wong LCH, Chanana P, Jaye A, Evans JM, FitzPatrick DR, Evans MJ, Fleming P, Jeffrey I, Cohen MC, Tfelt-Hansen J, Simpson MA, Behr ER, Ackerman MJ.

J Am Coll Cardiol. 2018 Mar 20;71(11):1217-1227. doi: 10.1016/j.jacc.2018.01.030.

PMID:
29544605
12.

Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.

Bacalhau M, Simões M, Rocha MC, Hardy SA, Vincent AE, Durães J, Macário MC, Santos MJ, Rebelo O, Lopes C, Pratas J, Mendes C, Zuzarte M, Rego AC, Girão H, Wong LC, Taylor RW, Grazina M.

Neuromuscul Disord. 2018 Apr;28(4):350-360. doi: 10.1016/j.nmd.2017.11.006. Epub 2017 Nov 23.

13.

MPV17-related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects.

El-Hattab AW, Wang J, Dai H, Almannai M, Staufner C, Alfadhel M, Gambello MJ, Prasun P, Raza S, Lyons HJ, Afqi M, Saleh MAM, Faqeih EA, Alzaidan HI, Alshenqiti A, Flore LA, Hertecant J, Sacharow S, Barbouth DS, Murayama K, Shah AA, Lin HC, Wong LC.

Hum Mutat. 2018 Apr;39(4):461-470. doi: 10.1002/humu.23387. Epub 2018 Jan 13.

PMID:
29282788
14.

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes.

Sadikovic B, Wang J, El-Hattab AW, Landsverk M, Douglas G, Brundage EK, Craigen WJ, Schmitt ES, Wong LC.

PLoS One. 2017 Nov 20;12(11):e0188610. doi: 10.1371/journal.pone.0188610. eCollection 2017.

15.

Long-term outcomes after reirradiation in nasopharyngeal carcinoma with intensity-modulated radiotherapy: A meta-analysis.

Leong YH, Soon YY, Lee KM, Wong LC, Tham IWK, Ho FCH.

Head Neck. 2018 Mar;40(3):622-631. doi: 10.1002/hed.24993. Epub 2017 Nov 11. Review.

PMID:
29130584
16.

Molecular and clinical spectra of FBXL4 deficiency.

El-Hattab AW, Dai H, Almannai M, Wang J, Faqeih EA, Al Asmari A, Saleh MAM, Elamin MAO, Alfadhel M, Alkuraya FS, Hashem M, Aldosary MS, Almass R, Almutairi FB, Alsagob M, Al-Owain M, Al-Sharfa S, Al-Hassnan ZN, Rahbeeni Z, Al-Muhaizea MA, Makhseed N, Foskett GK, Stevenson DA, Gomez-Ospina N, Lee C, Boles RG, Schrier Vergano SA, Wortmann SB, Sperl W, Opladen T, Hoffmann GF, Hempel M, Prokisch H, Alhaddad B, Mayr JA, Chan W, Kaya N, Wong LC.

Hum Mutat. 2017 Dec;38(12):1649-1659. doi: 10.1002/humu.23341. Epub 2017 Oct 6. Review.

PMID:
28940506
17.

Prognostic stratification of patients with metastatic nasopharyngeal carcinoma using a clinical and biochemical scoring system.

Chee J, Loh KS, Tham I, Ho F, Wong LC, Tan CS, Goh BC, Lim CM.

J Cancer Res Clin Oncol. 2017 Dec;143(12):2563-2570. doi: 10.1007/s00432-017-2496-1. Epub 2017 Aug 28.

PMID:
28849413
18.

Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ.

PLoS One. 2017 Aug 10;12(8):e0183406. doi: 10.1371/journal.pone.0183406. eCollection 2017.

19.

The phenotypic variability of HK1-associated retinal dystrophy.

Yuan Z, Li B, Xu M, Chang EY, Li H, Yang L, Wu S, Soens ZT, Li Y, Wong LC, Lewis RA, Sui R, Chen R.

Sci Rep. 2017 Aug 1;7(1):7051. doi: 10.1038/s41598-017-07629-3.

20.

Fulminant multicentric Castleman's disease in a patient with well-controlled human immunodeficiency virus infection-lessons from the patient.

Chen TC, Tseng HH, Wong LC.

J Formos Med Assoc. 2018 Mar;117(3):244-246. doi: 10.1016/j.jfma.2017.06.008. Epub 2017 Jun 27. No abstract available.

21.

Next generation deep sequencing corrects diagnostic pitfalls of traditional molecular approach in a patient with prenatal onset of Pompe disease.

Tsai AC, Hung YW, Harding C, Koeller DM, Wang J, Wong LC.

Am J Med Genet A. 2017 Sep;173(9):2500-2504. doi: 10.1002/ajmg.a.38333. Epub 2017 Jun 28.

PMID:
28657663
22.

Reduced Susceptibility to Antiseptics Is Conferred by Heterologous Housekeeping Genes.

Tansirichaiya S, Reynolds LJ, Cristarella G, Wong LC, Rosendahl K, Roberts AP.

Microb Drug Resist. 2018 Mar;24(2):105-112. doi: 10.1089/mdr.2017.0105. Epub 2017 Jun 12.

PMID:
28604259
23.

Lutein improves cell viability and reduces Alu RNA accumulation in hydrogen peroxide challenged retinal pigment epithelial cells.

Chong YS, Mai CW, Leong CO, Wong LC.

Cutan Ocul Toxicol. 2018 Mar;37(1):52-60. doi: 10.1080/15569527.2017.1335748. Epub 2017 Jun 20.

PMID:
28554225
24.

Dr. Maureen Rogers, the first Australian pediatric dermatologist.

Wong LC.

Int J Womens Dermatol. 2016 Jul 4;2(3):102-107. doi: 10.1016/j.ijwd.2016.05.002. eCollection 2016 Sep. No abstract available.

25.

Linking newborn severe combined immunodeficiency screening with targeted exome sequencing: A case report.

Patel DR, Yu H, Wong LC, Lupski JR, Seeborg FO, Rider NL, Martinez CA, Orange JS, Hanson C.

J Allergy Clin Immunol Pract. 2017 Sep - Oct;5(5):1442-1444. doi: 10.1016/j.jaip.2017.03.004. Epub 2017 Apr 21. No abstract available.

PMID:
28438538
26.

Tourette Syndrome as an Independent Risk Factor for Subsequent Sleep Disorders in Children: A Nationwide Population-Based Case-Control Study.

Lee WT, Huang HL, Wong LC, Weng WC, Vasylenko T, Jong YJ, Lin WS, Ho SY.

Sleep. 2017 Mar 1;40(3). doi: 10.1093/sleep/zsw072.

PMID:
28364427
27.

A curious case of neuromyelitis optica spectrum disorder co-existing with idiopathic intracranial hypertension.

Viswanathan S, Wong LC.

J Clin Neurosci. 2017 Jul;41:104-106. doi: 10.1016/j.jocn.2017.03.026. Epub 2017 Mar 23. No abstract available.

PMID:
28343917
28.

Altered resting-state EEG complexity in children with Tourette syndrome: A preliminary study.

Weng WC, Chang CF, Wong LC, Lin JH, Lee WT, Shieh JS.

Neuropsychology. 2017 May;31(4):395-402. doi: 10.1037/neu0000363. Epub 2017 Mar 20.

PMID:
28318282
29.

Consensus statement for the treatment of infantile haemangiomas with propranolol.

Smithson SL, Rademaker M, Adams S, Bade S, Bekhor P, Davidson S, Dore A, Drummond C, Fischer G, Gin A, Grills C, Halbert A, Lokmic Z, McCahon E, Morgan VA, Murrell DF, Orchard D, Penington A, Purvis D, Relic J, Robertson S, Robinson AJ, Scardamaglia L, Su J, Tan S, Wargon O, Warren L, Wong LC, Zappala T, Phillips R.

Australas J Dermatol. 2017 May;58(2):155-159. doi: 10.1111/ajd.12600. Epub 2017 Mar 1.

PMID:
28251611
30.

Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ.

PLoS One. 2017 Feb 9;12(2):e0170517. doi: 10.1371/journal.pone.0170517. eCollection 2017. Erratum in: PLoS One. 2017 Aug 10;12 (8):e0183406.

31.

Studies relating to the synthesis, enzymatic reduction and cytotoxicity of a series of nitroaromatic prodrugs.

Burke PJ, Wong LC, Jenkins TC, Knox RJ, Meikle IT, Stanforth SP.

Bioorg Med Chem Lett. 2016 Dec 15;26(24):5851-5854. doi: 10.1016/j.bmcl.2016.11.024. Epub 2016 Nov 11.

PMID:
27876476
32.

Improved Diagnosis of Inherited Retinal Dystrophies by High-Fidelity PCR of ORF15 followed by Next-Generation Sequencing.

Li J, Tang J, Feng Y, Xu M, Chen R, Zou X, Sui R, Chang EY, Lewis RA, Zhang VW, Wang J, Wong LC.

J Mol Diagn. 2016 Nov;18(6):817-824. doi: 10.1016/j.jmoldx.2016.06.007. Epub 2016 Sep 10.

PMID:
27620828
33.

Identification of KLHL40 mutations by targeted next-generation sequencing facilitated a prenatal diagnosis in a family with three consecutive affected fetuses with fetal akinesia deformation sequence.

Chen TH, Tian X, Kuo PL, Pan HP, Wong LC, Jong YJ.

Prenat Diagn. 2016 Dec;36(12):1135-1138. doi: 10.1002/pd.4949. Epub 2016 Nov 18.

PMID:
27762439
34.

Variations of movement disorders in anti-N-methyl-D-aspartate receptor encephalitis: A nationwide study in Taiwan.

Duan BC, Weng WC, Lin KL, Wong LC, Li ST, Hsu MH, Lin JJ, Fan PC, Lin MI, Chiu NC, Lin YC, Wang HS, Hung KL, Lee WT.

Medicine (Baltimore). 2016 Sep;95(37):e4365. doi: 10.1097/MD.0000000000004365.

35.

Frequency and Complexity of De Novo Structural Mutation in Autism.

Brandler WM, Antaki D, Gujral M, Noor A, Rosanio G, Chapman TR, Barrera DJ, Lin GN, Malhotra D, Watts AC, Wong LC, Estabillo JA, Gadomski TE, Hong O, Fajardo KV, Bhandari A, Owen R, Baughn M, Yuan J, Solomon T, Moyzis AG, Maile MS, Sanders SJ, Reiner GE, Vaux KK, Strom CM, Zhang K, Muotri AR, Akshoomoff N, Leal SM, Pierce K, Courchesne E, Iakoucheva LM, Corsello C, Sebat J.

Am J Hum Genet. 2016 Apr 7;98(4):667-79. doi: 10.1016/j.ajhg.2016.02.018. Epub 2016 Mar 24.

36.

Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing.

Qin L, Wang J, Tian X, Yu H, Truong C, Mitchell JJ, Wierenga KJ, Craigen WJ, Zhang VW, Wong LC.

J Mol Diagn. 2016 May;18(3):446-453. doi: 10.1016/j.jmoldx.2016.01.002. Epub 2016 Mar 2.

PMID:
26944031
37.

Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer.

Park JH, Vithayathil S, Kumar S, Sung PL, Dobrolecki LE, Putluri V, Bhat VB, Bhowmik SK, Gupta V, Arora K, Wu D, Tsouko E, Zhang Y, Maity S, Donti TR, Graham BH, Frigo DE, Coarfa C, Yotnda P, Putluri N, Sreekumar A, Lewis MT, Creighton CJ, Wong LC, Kaipparettu BA.

Cell Rep. 2016 Mar 8;14(9):2154-2165. doi: 10.1016/j.celrep.2016.02.004. Epub 2016 Feb 25.

38.

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.

Andorin A, Behr ER, Denjoy I, Crotti L, Dagradi F, Jesel L, Sacher F, Petit B, Mabo P, Maltret A, Wong LC, Degand B, Bertaux G, Maury P, Dulac Y, Delasalle B, Gourraud JB, Babuty D, Blom NA, Schwartz PJ, Wilde AA, Probst V.

Heart Rhythm. 2016 Jun;13(6):1274-82. doi: 10.1016/j.hrthm.2016.02.013. Epub 2016 Feb 24.

PMID:
26921764
39.

Effective Modulation of Male Aggression through Lateral Septum to Medial Hypothalamus Projection.

Wong LC, Wang L, D'Amour JA, Yumita T, Chen G, Yamaguchi T, Chang BC, Bernstein H, You X, Feng JE, Froemke RC, Lin D.

Curr Biol. 2016 Mar 7;26(5):593-604. doi: 10.1016/j.cub.2015.12.065. Epub 2016 Feb 11.

40.

Recruitment of Asians and Pacific Islanders with Type 2 Diabetes into a Clinical Research Trial of Enhancing Diabetes Self-Management.

Wong LC, Ribeiro M, Vasquez-Brooks M, Estrella D, Wang CY, Arakaki R, Inouye J.

J Cult Divers. 2015 Winter;22(4):142-7.

PMID:
26817172
41.

Increased risk of epilepsy in children with Tourette syndrome: A population-based case-control study.

Wong LC, Huang HL, Weng WC, Jong YJ, Yin YJ, Chen HA, Lee WT, Ho SY.

Res Dev Disabil. 2016 Apr-May;51-52:181-7. doi: 10.1016/j.ridd.2015.10.005. Epub 2015 Nov 18.

PMID:
26597416
42.

Increased risks of tic disorders in children with epilepsy: A nation-wide population-based case-control study in Taiwan.

Weng WC, Huang HL, Wong LC, Jong YJ, Yin YJ, Chen HA, Lee WT, Ho SY.

Res Dev Disabil. 2016 Apr-May;51-52:173-80. doi: 10.1016/j.ridd.2015.10.019. Epub 2015 Nov 12.

PMID:
26585639
43.

Author's reply: To PMID 24585884.

Wong LC, Behr ER.

Europace. 2015 Nov;17(11):1739-40. doi: 10.1093/europace/euv094. Epub 2015 Jun 7. No abstract available.

PMID:
26056186
44.

STIM2 regulates PKA-dependent phosphorylation and trafficking of AMPARs.

Garcia-Alvarez G, Lu B, Yap KA, Wong LC, Thevathasan JV, Lim L, Ji F, Tan KW, Mancuso JJ, Tang W, Poon SY, Augustine GJ, Fivaz M.

Mol Biol Cell. 2015 Mar 15;26(6):1141-59. doi: 10.1091/mbc.E14-07-1222. Epub 2015 Jan 21.

45.

An in-tumor genetic screen reveals that the BET bromodomain protein, BRD4, is a potential therapeutic target in ovarian carcinoma.

Baratta MG, Schinzel AC, Zwang Y, Bandopadhayay P, Bowman-Colin C, Kutt J, Curtis J, Piao H, Wong LC, Kung AL, Beroukhim R, Bradner JE, Drapkin R, Hahn WC, Liu JF, Livingston DM.

Proc Natl Acad Sci U S A. 2015 Jan 6;112(1):232-7. doi: 10.1073/pnas.1422165112. Epub 2014 Dec 22.

46.

Two patients with Hashimoto's encephalopathy and uncontrolled diabetes successfully treated with levetiracetam.

Wong LC, Freeburg JD, Montouris GD, Hohler AD.

J Neurol Sci. 2015 Jan 15;348(1-2):251-2. doi: 10.1016/j.jns.2014.11.007. Epub 2014 Nov 13.

PMID:
25467138
47.

Determinants of an effective antibiotic campaign: Lessons from Hong Kong.

Ho ML, Cowling BJ, Seto WH, Wong LC, Wong TY.

J Glob Antimicrob Resist. 2014 Dec;2(4):334-337. doi: 10.1016/j.jgar.2014.08.001. Epub 2014 Aug 29.

PMID:
27873698
48.

Clinical outcome of palliative radiotherapy for locally advanced symptomatic gastric cancer in the modern era.

Tey J, Choo BA, Leong CN, Loy EY, Wong LC, Lim K, Lu JJ, Koh WY.

Medicine (Baltimore). 2014 Nov;93(22):e118. doi: 10.1097/MD.0000000000000118.

49.

A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomalies.

Landsverk ML, Zhang VW, Wong LC, Andersson HC.

Mol Genet Metab Rep. 2014 Oct 14;1:451-454. eCollection 2014.

50.

Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience.

Wong LC, Roses-Noguer F, Till JA, Behr ER.

Circ Arrhythm Electrophysiol. 2014 Oct;7(5):800-6. doi: 10.1161/CIRCEP.114.001818. Epub 2014 Sep 6.

PMID:
25194972

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