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Items: 1 to 50 of 222

1.

Burden in caregivers of adults with epilepsy in Asian families.

Lai ST, Tan WY, Wo MC, Lim KS, Ahmad SB, Tan CT.

Seizure. 2019 Oct;71:132-139. doi: 10.1016/j.seizure.2019.07.008. Epub 2019 Jul 8.

PMID:
31325820
2.

Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex.

Chen CP, Chang SY, Huang MC, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):769-771. doi: 10.1016/j.tjog.2018.08.032. No abstract available.

3.

Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay.

Chen CP, Chang SY, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):765-768. doi: 10.1016/j.tjog.2018.08.031. No abstract available.

4.

First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome.

Chen CP, Chang SY, Lau HS, Chen SW, Lai ST, Chuang TY, Lee MS, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):763-764. doi: 10.1016/j.tjog.2018.08.030. No abstract available.

5.

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.

Chen CP, Chang SY, Chen YN, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):739-744. doi: 10.1016/j.tjog.2018.08.024.

6.

Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.

Chen CP, Chang SY, Lin CJ, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):734-738. doi: 10.1016/j.tjog.2018.08.023.

7.

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.

Chen CP, Chang SY, Wang LK, Chang TY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Town DD, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2018 Oct;57(5):730-733. doi: 10.1016/j.tjog.2018.08.022.

8.

Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.

Lai ST, Chen CP, Lin CJ, Chen YN, Chen SW.

J Med Ultrasound. 2018 Jul-Sep;26(3):170. doi: 10.4103/JMU.JMU_75_18. Epub 2018 Sep 14. No abstract available.

9.

A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints.

Chen CP, Lin SP, Chern SR, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):608-610. doi: 10.1016/j.tjog.2018.06.025. No abstract available.

10.

A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows.

Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):583-587. doi: 10.1016/j.tjog.2018.06.019.

11.

Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.

Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2018 Aug;57(4):578-582. doi: 10.1016/j.tjog.2018.06.018.

12.

An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus.

Lai ST, Chen CP, Lin CJ, Chen YN, Chen SW.

J Med Ultrasound. 2017 Oct-Dec;25(4):255-257. doi: 10.1016/j.jmu.2017.06.002. Epub 2017 Aug 9. No abstract available.

13.

An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus.

Lai ST, Chen CP, Lin CJ, Chen YN, Chen SW.

J Med Ultrasound. 2017 Jul-Sep;25(3):188-189. doi: 10.1016/j.jmu.2017.06.001. Epub 2017 Aug 4. No abstract available.

14.

Positive psychological interventions for neurological disorders: A systematic review.

Lai ST, Lim KS, Low WY, Tang V.

Clin Neuropsychol. 2019 Apr;33(3):490-518. doi: 10.1080/13854046.2018.1489562. Epub 2018 Jun 24.

PMID:
29938575
15.

Late-onset fetal bilateral pleural effusions associated with Down syndrome.

Lai ST, Chen CP, Lin CJ, Hsu CY, Wu PS, Lee CC, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):133-136. doi: 10.1016/j.tjog.2018.01.001.

16.

Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities.

Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):128-132. doi: 10.1016/j.tjog.2017.12.022.

17.

Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus.

Chen CP, Ko TM, Chang TY, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):123-127. doi: 10.1016/j.tjog.2017.12.021.

18.

Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia.

Chen CP, Chang TY, Lin TW, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):119-122. doi: 10.1016/j.tjog.2017.12.020. Review.

19.

Positive psychological interventions for people with epilepsy: An assessment on factors related to intervention participation.

Lai ST, Lim KS, Tang V, Low WY.

Epilepsy Behav. 2018 Mar;80:90-97. doi: 10.1016/j.yebeh.2017.12.019. Epub 2018 Feb 3.

PMID:
29414564
20.

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.

Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):852-856. doi: 10.1016/j.tjog.2017.10.034.

21.

Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.

Chen CP, Hsieh CH, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):847-851. doi: 10.1016/j.tjog.2017.10.027.

22.

Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.

Chen CP, Chang TY, Hung FY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):843-846. doi: 10.1016/j.tjog.2017.10.026.

23.

Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome.

Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):840-842. doi: 10.1016/j.tjog.2017.10.025.

24.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):836-839. doi: 10.1016/j.tjog.2017.10.024.

25.

Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.

Taiwan J Obstet Gynecol. 2017 Dec;56(6):821-826. doi: 10.1016/j.tjog.2017.10.021.

26.

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.

Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Oct;56(5):691-693. doi: 10.1016/j.tjog.2017.09.001.

27.

Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome.

Chen CP, Huang JP, Chern SR, Chen SW, Lai ST, Wu PS, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):569-570. doi: 10.1016/j.tjog.2017.05.007. No abstract available.

28.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21.

Chen CP, Chen M, Chern SR, Chang SP, Chen SW, Lai ST, Chen WL, Lee MS, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):566-568. doi: 10.1016/j.tjog.2017.05.006. No abstract available.

29.

Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect.

Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Lee CC, Yang CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):550-553. doi: 10.1016/j.tjog.2017.06.003.

30.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.

Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):545-549. doi: 10.1016/j.tjog.2017.05.004.

31.

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.

Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chang SP, Yang CW, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Aug;56(4):527-533. doi: 10.1016/j.tjog.2017.06.002.

32.

Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.

Chen CP, Lin SP, Liu YP, Chern SR, Chen SW, Lai ST, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):412-414. doi: 10.1016/j.tjog.2017.04.030. No abstract available.

33.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions.

Chen CP, Chen M, Hwu YM, Chang SP, Chen SW, Lai ST, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):410-411. doi: 10.1016/j.tjog.2017.04.029. No abstract available.

34.
35.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.

Chen CP, Chen M, Wang PT, Chern SR, Chen SW, Lai ST, Wu PS, Chang SP, Pan CW, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):394-397. doi: 10.1016/j.tjog.2017.04.025.

36.

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome.

Chen CP, Yin CS, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Chen WL, Wang W.

Taiwan J Obstet Gynecol. 2017 Jun;56(3):390-393. doi: 10.1016/j.tjog.2017.04.024.

37.
38.

Novel synthetic kojic acid-methimazole derivatives inhibit mushroom tyrosinase and melanogenesis.

Chen MJ, Hung CC, Chen YR, Lai ST, Chan CF.

J Biosci Bioeng. 2016 Dec;122(6):666-672. doi: 10.1016/j.jbiosc.2016.06.002. Epub 2016 Jun 25.

PMID:
27353860
39.

Skin whitening capability of shikimic acid pathway compound.

Chen YH, Huang L, Wen ZH, Zhang C, Liang CH, Lai ST, Luo LZ, Wang YY, Wang GH.

Eur Rev Med Pharmacol Sci. 2016;20(6):1214-20.

40.

Radiosensitization of metformin in pancreatic cancer cells via abrogating the G2 checkpoint and inhibiting DNA damage repair.

Wang Z, Lai ST, Ma NY, Deng Y, Liu Y, Wei DP, Zhao JD, Jiang GL.

Cancer Lett. 2015 Dec 1;369(1):192-201. doi: 10.1016/j.canlet.2015.08.015. Epub 2015 Aug 21.

PMID:
26304716
41.

Kinetics of mushroom tyrosinase and melanogenesis inhibition by N-acetyl-pentapeptides.

Lien CY, Chen CY, Lai ST, Chan CF.

ScientificWorldJournal. 2014;2014:409783. doi: 10.1155/2014/409783. Epub 2014 Jul 22.

42.

Metformin is associated with reduced risk of pancreatic cancer in patients with type 2 diabetes mellitus: a systematic review and meta-analysis.

Wang Z, Lai ST, Xie L, Zhao JD, Ma NY, Zhu J, Ren ZG, Jiang GL.

Diabetes Res Clin Pract. 2014 Oct;106(1):19-26. doi: 10.1016/j.diabres.2014.04.007. Epub 2014 Apr 18. Review.

PMID:
24837144
43.

Prosthetic mitral valve obstructed by occluder device for paravalvular leak.

Lai ST, Fu YC, Chan SW, Tsai HW.

Ann Thorac Surg. 2014 May;97(5):1807. doi: 10.1016/j.athoracsur.2013.10.063. No abstract available.

PMID:
24792278
44.

Look-back investigation of a health care worker infected with human immunodeficiency virus.

Lam TH, Tsang DN, Lo JY, Gold J, Luk HT, Lai ST, Ho MY, Tsao J, Wong KH.

Am J Infect Control. 2014 May;42(5):569-70. doi: 10.1016/j.ajic.2014.01.014.

PMID:
24773799
45.

Inhibitory effects of novel synthetic methimazole derivatives on mushroom tyrosinase and melanogenesis.

Chan CF, Lai ST, Guo YC, Chen MJ.

Bioorg Med Chem. 2014 May 1;22(9):2809-15. doi: 10.1016/j.bmc.2014.03.009. Epub 2014 Mar 15.

46.

Safety and efficacy of nimotuzumab in combination with radiotherapy for patients with squamous cell carcinoma of the esophagus.

Ma NY, Cai XW, Fu XL, Li Y, Zhou XY, Wu XH, Hu XC, Fan M, Xiang JQ, Zhang YW, Chen HQ, Lai ST, Jiang GL, Zhao KL.

Int J Clin Oncol. 2014 Apr;19(2):297-302. doi: 10.1007/s10147-013-0564-3. Epub 2013 May 21.

PMID:
23690261
47.

Short-term results of catheter-directed intrathrombus thrombolysis versus anticoagulation in acute proximal deep vein thrombosis.

Lee CY, Lai ST, Shih CC, Wu TC.

J Chin Med Assoc. 2013 May;76(5):265-70. doi: 10.1016/j.jcma.2013.01.006. Epub 2013 Apr 12.

48.

Use of biologics for inflammatory bowel disease in Hong Kong: consensus statement.

Leung WK, Ng SC, Chow DK, Lao WC, Leung VK, Li MK, Hui YT, Ng SS, Hui AJ, Lai ST, Lam JT, Poon JT, Chan AO, Yuen H, Wu JC; Hong Kong IBD Society; Hong Kong IBD Society.

Hong Kong Med J. 2013 Feb;19(1):61-8.

49.

Mediastinal diffuse large B-cell lymphoma invading the left atrium mimicking coronary artery disease with a mural thrombus.

Yang CC, Tsai HW, Lai ST, Wu HC, Lo CY, Chang Y.

J Chin Med Assoc. 2012 Nov;75(11):606-9. doi: 10.1016/j.jcma.2012.08.009. Epub 2012 Oct 10.

50.

Hong Kong experiences the 'Ultimate superbug': NDM-1 Enterobacteriaceae.

Tsang KY, Luk S, Lo JY, Tsang TY, Lai ST, Ng TK.

Hong Kong Med J. 2012 Oct;18(5):439-41.

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