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鼻咽喉内镜检查对儿童上气道咳嗽综合征的病因分析及诊断价值 被引量:14
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作者 敬尚林 林楠 +4 位作者 唐向荣 莫炼 温慧 杨艳 胡江锋 《中国内镜杂志》 北大核心 2017年第11期10-13,共4页
目的探讨鼻咽喉内镜检查对儿童上气道咳嗽综合征(UACS)的病因分析及诊断方面的应用价值。方法对该院2014年1月-2016年12月确诊为UACS的132例患儿经鼻咽喉内镜检查的结果进行分析研究。结果 132例患儿中发现有上气道病变因素者125例(94.7... 目的探讨鼻咽喉内镜检查对儿童上气道咳嗽综合征(UACS)的病因分析及诊断方面的应用价值。方法对该院2014年1月-2016年12月确诊为UACS的132例患儿经鼻咽喉内镜检查的结果进行分析研究。结果 132例患儿中发现有上气道病变因素者125例(94.70%)。其中,常见因素为鼻窦炎43例(32.58%),慢性鼻炎32例(24.24%),腺样体肥大13例(9.85%),慢性咽炎11例(8.33%),慢性扁桃体炎(扁桃体肥大)9例(6.82%)。在不同年龄段中,上气道病变因素分布有所不同,差异有统计学意义(P<0.05)。结论鼻咽喉内镜检查在UACS病因分析及诊断中能够准确、及时发现上气道局部病变情况,为临床精准诊治提供良好帮助,是一种安全有效的检查方法,在临床上值得推广使用。 展开更多
关键词 鼻咽喉内镜 儿童 上气道咳嗽综合征 病因诊断
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Detection of hepatitis B virus genotypes using oligonucleotide chip among hepatitis B virus carriers in Eastern China 被引量:7
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作者 xiang-rong tang Ji-Shen Zhang +3 位作者 Hui Zhao Yu-Hua Gong Yong-Zhong Wang Jian-Long Zhao 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第13期1975-1979,共5页
AIM: TO determine the genotype distribution of hepatitis B virus (HBV) with a newly oligonucleotide chip assay among the HBV carriers in Eastern China. METHODS: An assay using oligonucleotide chip was developed fo... AIM: TO determine the genotype distribution of hepatitis B virus (HBV) with a newly oligonucleotide chip assay among the HBV carriers in Eastern China. METHODS: An assay using oligonucleotide chip was developed for detection of HBV genotypes in serum samples from HBV DNA-positive patients in Eastern China. This method is based on the principle of reverse hybridization with Cy5-labeled amplicons hybridizing to type-specific oligonucleotide probes that are immobilized on slides. The results of 80 randomly chosen sera were confirmed by direct sequencing. RESULTS: HBV genotype B, C and mixed genotype were detected in 400 serum samples, accounting for 8.3% (n = 33), 83.2% (n = 333), and 8.5% (n = 34), respectively. The evaluation of the oligonucleotide assay showed 100% concordance with the amplicon phylogenetic analysis except 9 mixed genotype infections undetected by sequencing. CONCLUSION: The study indicates that HBV genotype C and B prevail in the Eastern China. It is suggested that the oligonucleotide chip is a reliable and convenient tool for the detection of HBV genotyping. 展开更多
关键词 Oligonucleotide chip Hepatitis B virus GENOTYPE
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Patients with MMAF induced by novel biallelic CFAP43 mutations have good fertility outcomes after intracytoplasmic sperm injection 被引量:1
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作者 Jing Ma Shun-Hua Long +8 位作者 Hai-Bing Yu Ye-Zhou Xiang xiang-rong tang Jia-Xun Li Wei-Wei Liu Wei Han Rong Jin Guo-Ning Huang Ting-Ting Lin 《Asian Journal of Andrology》 SCIE CAS CSCD 2023年第5期564-571,共8页
As a specific type of asthenoteratozoospermia,multiple morphological abnormalities of the sperm flagella(MMAF)is characterized by composite abnormalities,including absent,short,coiled,angulation,and irregular-caliber ... As a specific type of asthenoteratozoospermia,multiple morphological abnormalities of the sperm flagella(MMAF)is characterized by composite abnormalities,including absent,short,coiled,angulation,and irregular-caliber flagella.Mutations in cilia-and flagella-associated protein 43(CFAP43)are one of the main causative factors of MMAF established to date.To identify whether there are other CFAP43 mutations related to MMAF and to determine the clinical outcomes of assisted reproductive technology for patients with MMAF harboring different mutations,we recruited and screened 30 MMAF-affected Chinese men using a 22-gene next-generation sequencing panel.After systematic analysis,seven mutations in CFAP43,including five novel mutations and two previously reported mutations,were identified from four families and related to MMAF in an autosomal recessive pattern.Papanicolaou staining,immunofluorescence,and electronic microscopy further clarified the semen characteristics a nd abnormal sperm morphologies,including disorganized axonemal and peri-axonemal structures,of the CFAP43-deficient men.The female partners of two patients were pregnant after undergoing assisted reproductive technology through intracytoplasmic sperm injection,and one of them successfully gave birth to a healthy boy.This study significantly expands the mutant spectrum of CFAP43,and together with the available information regarding male infertility and MMAF,provides new information for the genetic diagnosis and counseling of MMAF in the future. 展开更多
关键词 asthenoteratozoospermia CFAP43 intracytoplasmic sperm injection MMAF
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