巨结肠

神经元特异性稀醇化酶和S-100蛋白免疫组化染色在先天性巨结肠诊断中的应用

Application of Neuron-Specific Enolase and S-100 Protein in Diagnosis of Hirschsprung 's Disease

先天性巨结肠术中冰冻切片的可靠性

Reliability of intraoperative frozen sections in the management of Hirschsprung 's disease

先天性巨结肠内皮素B受体基因突变的研究

Mutation of endothelin B receptor gene in Hirschsprung 's disease

先天性巨结肠神经营养因子-3、酪氨酸激酶C的表达及其意义

Expression of neurotrophin 3 and tyrosine kinase C in Hirschsprung 's disease and its significance

内皮素B受体基因与先天性巨结肠关系的研究进展

Advances in research of the relationship between endothelin receptor type B and Hirschsprung 's disease

先天性巨结肠（Hirschsprung'SDisease，HD）是常见的先天性消化道畸形，其病因尚未明了。

The etiology of Hirschsprung 's disease ( HD ) which is a common congenital malformation of the digestive tract remains unclear .

目的：先天性巨结肠症（Hirschsprung'SDisease，HD）是以肠神经系统缺陷、肠神经节细胞缺失为主要特征的常见的胃肠道发育畸形。

Objective : Hirschsprung 's Disease ( HD ) is a common congenital disease characterized by aganglionic , lack of the normal bowel movement .

LN、Ⅳ-C和HA在先天性巨结肠症肠壁平滑肌中的表达及其意义

The Expression and Significance of LN , ⅳ - C and HA in Smooth Muscle of Colon in HD

PCR-SSCP法检测先天性巨结肠酪氨酸激酶受体基因突变

Detection of RET gene mutations in Hirschsprung disease by PCR-SSCP method

先天性巨结肠症（congenitalmegacolon）又称为赫希施普龙病（Hirschsprung'SDisease，HD）是一种比较常见的胃肠道畸形。

Congenital megacolon is also called Hirschsprung 's disease , HD . It 's a common gastrointestinal abnormality in children .

中国人先天性巨结肠RET基因突变及Bcl-2的表达

The research on the mutation feature of exon 13 of RET gene in Chinese Hirschsprung 's disease

结论腹部平片异常可提示巨结肠，是诊断TCA的首选方法；

Conclusion Abdomen plain film examination is the first method to TCA .

先天性巨结肠与其同源病的RET基因突变的研究

Mutations of RET proto-oncogene in Hirschsprung 's disease and its allied disorders

先天性巨结肠RET蛋白免疫组化研究

Immunohistochemical Study of RET Protein In Hirschsprung 's Desease

PGP9.5和S-100蛋白在先天性巨结肠诊断中的应用

The Application of PGP 9.5 and S-100 Protein Immunohistochemical Method in the Diagnosis of HD

S-100，SY在先天性巨结肠中的表达及其临床意义

The Expression of Soluble-protein and Synaptophysin in Hirschsprung 's Disease and its Clinical Significance

NSE和S-100蛋白在巨结肠同源病的表达

Expression of NSE and S-100 Protein Immunohistochemical Markers in Hirschsprung 's Allied Disorder Legionnaires ' disease

1例室间隔缺损伴巨结肠VSD修补术后患者的护理

Nursing Care for a Patient with Ventricular Septal Defect and Hirschsprung Disease Undergoing VSD Closure Operation

成人HD需与肠结核、溃疡性结肠炎、特发性巨结肠相鉴别。

Adult HD differs from intestinal tuberculosis , ulcerative colonitis , idiopathic megacolon in case history , histological chemistry and pathology .

目的探讨先天性巨结肠（HD）根治术后并发小肠结肠炎（HEC）的防治经验。

Objective To explore the prophylaxis of enterocolitis for post-operation patients with Hirschsprung 's Disease ( HD ) .

RET基因多态性与中国湖北地区汉族人群先天性巨结肠的相关性研究

Association between RET proto-oncogene polymorphisms and Hirschsprung disease in Chinese Han population of Hubei district

目的探讨前腹壁悬吊（免气腹）腹腔镜辅助下婴儿先天性巨结肠（HD）根治术的特点。

Objective To investigate the feasibility of gasless laparoscopy-assisted surgery as an alternative method for neonate Hirschsprung ' disease ( HD ) .

先天性巨结肠Cajal间质细胞的研究

Interstitial cells of Cajal in Hirschsprung 's disease

Cajal间质细胞在先天性巨结肠不同肠段的分布

Distribution of Interstitial Cells of Cajal in Different Segments of Hirschsprung ′ s Disease

改良Duhamel术式治疗成人先天性巨结肠七例

Modified Duhamel operation on seven cases of adult Hirschsprung 's disease

目的研究先天性巨结肠（HD）的发生与内皮素B受体基因（EDNRB）突变间的关系。

Objective To investigate the relationship between endothelin B receptor gene and Hirschsprung 's disease ( HD ) in chinese .

目的本研究通过观察Cajal间质细胞（interstitialcellofCajal，ICC）在先天性巨结肠患者狭窄段、移行段、扩张段中的分布情况，探讨ICC在先天性巨结肠发病中的作用。

Objective The current study investigates the role of ICC ( interstitial cell of Cajal ) in the pathogenesis of Hirschsprung 's disease .

天津地区先天性巨结肠RET基因13号外显子基因多态性研究

Study of RET Proto-oncogene Exon 13 DNA Polymorphism in Patients with Hirschsprung 's Disease in Tianjin District

神经元特异烯醇化酶和S100蛋白在巨结肠及其类缘病中的表达

Expression of Neuron Specific Enolase and Soluble-Protein 100 in Hirschsprung ′ s Disease and Its Allied Disease

结论RET基因突变与家族性先天性巨结肠症的发生有关。

Conclusion Mutation of RET proto oncogene might play an role in the familial Hirschsprung ′ s disease .