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Phospho-histone H3 in Gastrointestinal Stromal Tumors Risk Stratification Evaluated by Manual Counting and Computer-Assisted Image Analysis [Meeting Abstract]

Huang, Yan; Nasim, Mansoor; Yang, Yihe; Lee, Lili
ISI:000429308602090
ISSN: 0893-3952
CID: 5516502

The Significance of Sessile Serrated Polyps in Inflammatory Bowel Disease

Jackson, Whitney E; Achkar, Jean-Paul; Macaron, Carole; Lee, Lili; Liu, Xiuli; Pai, Rish K; Lopez, Rocio; Burke, Carol A; Allende, Daniela S
BACKGROUND:The significance of serrated lesions in inflammatory bowel disease (IBD) remains unclear. We aim to characterize synchronous and metachronous lesions in IBD patients with an index serrated polyp and compare them to sporadic subjects with SSP. METHODS:Serrated lesions in patients with IBD were identified from a pathology database and, after review, were reclassified as hyperplastic (HP), sessile serrated (SSPs), or serrated polyps unclassifiable (SPU). RESULTS:One hundred thirty-four IBD patients were found to have 147 serrated polyps at index colonoscopy. SSPs were more likely to be located in the right colon: SSP (76.0%), SPU (41.7%) and HP (27.8%); P = 0.002. Synchronous multifocal visible dysplasia occurred more frequently in the SSP or SPU groups (44.5% and 66%) compared to the HP group (12%); P = 0.031. Among 13 IBD patients with index SSP followed over a median of 6 years, 61.5% developed metachronous visible dysplasia or additional SSPs. Larger index SSP size was associated with higher risk of developing subsequent visible dysplasia with a 10% increase for every 1 mm increase in size (HR = 1.1; P = 0.028), but was not associated with developing subsequent SSP (P = 0.50). The risk of subsequent SSP or visible dysplasia was no different between the IBD and non-IBD groups, but there was a trend suggesting SSP may be a marker of increased early risk of metachronous visible dysplasia in IBD patients. CONCLUSIONS:IBD patients with an index SSP and SPU have a heightened risk of synchronous multifocal visible dysplasia. Additionally, IBD patients with SSP may be at risk of early metachronous visible dysplasia.
PMID: 27508509
ISSN: 1536-4844
CID: 5038652

Molecular epidemiology of measles virus in Taiwan in 2010-2011: the common genotype changed from H1 to D9 and the first appearance of D4

Cheng, Wen-Yueh; Tung, Hsiao-Ping; Wang, Hsiao-Chi; Lee, Li-Li; Wu, Ho-Sheng; Liu, Ming-Tsan
Measles has been controlled effectively in some countries because of high coverage rates with an effective vaccine. However, measles outbreaks still occasionally occur in areas with high vaccine coverage as a result of imported transmission. To identify the sources of measles infection and to determine whether measles cases are part of a single outbreak or due to multiple importations, measles virus (MV) genotyping is required and plays an important role in MV elimination. In Taiwan, genotype H1 of MV was detected most frequently before 2009. From 2006 to 2011, 47 of 48 genotype H1 cases were associated with the imported cases, indicating that genotype H1 was not an endemic genotype in Taiwan after 2006. The distribution of the other genotypes (D3, D4, D5, D8, D9, and G3) detected during 2006-2011 varied by year. Taiwan has a pattern of measles genotypes that is consistent with the elimination of MV and with the absence of endemic genotypes. In this study, the genotypes of 40 cases of MV detected during 2010-2011 were investigated and analyzed. In 2010, the most common genotype changed from H1 (3/40) to D9 (35/40). In 2011, genotype H1 was not detected, and genotype D4 first appeared and was imported from Europe. The dynamic change of detected genotypes of MV in Taiwan is influenced by the activity of a measles control program in WHO regions. This study emphasizes that global synchronous elimination is important for an individual country or area to maintain free from MV.
PMID: 23588738
ISSN: 1096-9071
CID: 5038642

Molecular evolution of measles viruses circulated in Taiwan 1992-2008

Cheng, Wen-Yueh; Lee, Lili; Rota, Paul A; Yang, Dustin Chen-Fu
Genetic analyses of viral samples from 74 laboratory confirmed measles cases occurring in Taiwan during 1992-2008 identified six viral genotypes D3, D5, D9, G2, H1 and H2. The most frequently detected genotype, H1, was associated with outbreaks in 1994 and 2002, and was the likely indigenous genotype in 1992. In response to the outbreaks, two catch-up campaigns were launched and a routine second dose of measles, mumps, and rubella vaccine at entry to elementary school was introduced. The vaccination campaigns successfully reduced the number of measles cases in Taiwan, and many of the more recent cases can be traced to importations, primarily from other Asian countries. A number of measles genotypes which were associated with outbreaks in other Asian countries were detected among the more recent cases. The more recent genotype H1 viruses had sequences that were identical to those currently circulating in China or associated with international importation of virus.
PMCID:2797522
PMID: 20003242
ISSN: 1743-422x
CID: 5038632

Serologic and molecular biologic methods for SARS-associated coronavirus infection, Taiwan

Wu, Ho-Sheng; Chiu, Shu-Chun; Tseng, Tsan-Chang; Lin, Szu-Fong; Lin, Jih-Hui; Hsu, Yu-Hen; Wang, Mei-Ching; Lin, Tsuey-Li; Yang, Wen-Zieh; Ferng, Tian-Lin; Huang, Kai-Hung; Hsu, Li-Ching; Lee, Li-Li; Yang, Jyh-Yuan; Chen, Hour-Young; Su, Shun-Pi; Yang, Shih-Yan; Lin, Shih-Yan; Lin, Ting-Hsiang; Su, Ih-Sen
Severe acute respiratory syndrome (SARS) has raised a global alert since March 2003. After its causative agent, SARS-associated coronavirus (SARS-CoV), was confirmed, laboratory methods, including virus isolation, reverse transcriptase-polymerase chain reaction (RT-PCR), and serologic methods, have been quickly developed. In this study, we evaluated four serologic tests ( neutralization test, enzyme-linked immunosorbent assay [ELISA], immunofluorescent assay [IFA], and immunochromatographic test [ICT]) for detecting antibodies to SARS-CoV in sera of 537 probable SARS case-patients with correlation to the RT-PCR. With the neutralization test as a reference method, the sensitivity, specificity, positive predictive value, and negative predictive value were 98.2%, 98.7%, 98.7%, and 98.4% for ELISA; 99.1%, 87.8%, 88.1% and 99.1% for IFA; 33.6%, 98.2%, 95.7%, and 56.1% for ICT, respectively. We also compared the recombinant-based western blot with the whole virus-based IFA and ELISA; the data showed a high correlation between these methods, with an overall agreement of >90%. Our results provide a systematic analysis of serologic and molecular methods for evaluating SARS-CoV infection.
PMCID:3322922
PMID: 15030702
ISSN: 1080-6040
CID: 5038622