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| 1 | Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype46,XY,del(2) (q37) 显示文摘 | Gorski JL Cox BA Kyine M | 1989 | Am J Med Genet1989，32，3： | 1 |
| 2 | Refractory gold ores in Archaean greenstones, Western Australia: mineralogy, gold paragenesis, metallurgical charac- terization and classification显示文摘 | Vaughan J Kyin A | 2004 | Mineralogical Magazine2004，68，2： | 1 |
| 3 | The contribution of NKT cells, NK cells, and other gamma-chain-dependent non-T non-B cells to IL- 12-mediated rejection of tumors 显示文摘 | Park S H Kyin T Bendelac A | 2003 | J Immunol2003，170，3： | 1 |
| 4 | A thymic precursor to the NK T cell lineage 显示文摘 | Benlagha K Kyin T Beavis A | 2002 | Science2002，296，5567： | 1 |
| 5 | A thymic precursor to the NK T cell lineage显示文摘 | Benlagha K Kyin T Beavis A | 2002 | Science2002，296，5567： | 1 |
| 6 | A thymic precursor to the NKT cell lineage显示文摘 | Benlagha K Kyin T Beavis A | | 0，，： | 1 |
| 7 | A thymic precursor to the NK T cell lineage显示文摘 | Benlagha K Kyin T Beavis A | 2002 | Science2002，296，5567： | 1 |
| 8 | Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46, XY ,del (2)( q3 7) 显示文摘 | Gorski ]L Cox BA Kyine M | 1989 | Am J Med Genetics1989，32，3： | 1 |
| 9 | A thymic precursor to the NKT-cell lineage显示文摘 | Kyin T Beavis A | 2002 | Science2002，296，： | 1 |
| 10 | A thymic precursor to the NK T cell lineage显示文摘 | Benlagha K Kyin T Beavis A | 2002 | Science2002，296，5567： | 1 |
| 11 | Comparison of microscopy and PCR for the detection of human Plasmodium species and Plasmodium knowlesi in southern Myanmar显示文摘Objectives: To determine the distribution of Plasmodium(P) species including Plasmodium knowlesi and to compare the specificity and sensitivity of microscopy with nested PCR in malaria diagnosis.Methods: The study was conducted in Kawthaung, southern Myanmar. Ninety clinically suspected malaria patients were screened for malaria by Giemsa stained microscopy and con firmed by nested PCR.Results: Among the participants, 57(63.3%) were positive and 33(36.7%)were negative by microscopy. Of positive samples, 39(68.4%) were Plasmodium fcalciparum,17(29.8%) Plasmodium vivax and 1(1.8%) Plasmodium malariae, whereas 59-amplified by PCR were 40(67.8%), 18(30.5%) and 1(1.7%) respectively. PCR amplified 2 microscopy negative samples. Two samples of P. falciparum detected by microscopy were amplified as P. vivax and vice versa. All samples were negative for Plasmodium ovale.P. knowlesi and mixed infections. Microscopy had a very good measure of agreement(κ=0.95) compared to nested PCR. Sensitivity and specificity of microscopy for diagnosis of P. falciparum were 92.5%(95% CI: 79.6-98.4) and 96.0%(95% CI: 86.3-99.5)respectively, whereas for P. vivax were 83.3%(95% CI: 58.6-96.4) and 97.2%(95% CI:90.3-99.7).Conclusions: P. knowlesi was not detected by both microscopy and PCR. Giemsa stained microscopy can still be applied as primary method for malaria diagnosis and is considered as gold standard. As to the lower sensitivity of microscopy for vivax malaria,those with previous history of malaria and relapse cases should be diagnosed by RDT or PCR combined with microscopy. Inaccuracy of species diagnosis highlighted the requirement of training and refresher courses for microscopists. | Thu Zar Han Kay Thwe Han Kyin Hla Aye Thaung Hlaing Kyaw Zin Thant Indra Vythilingam | 2017 | Asian Pacific Journal of Tropical Biomedicine2017，7，8： | 0 |
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