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排序方式: 共有1946条查询结果,搜索用时 15 毫秒
1.
目的 探讨巴曲酶治疗全频下降型突发性耳聋的疗效与巴曲酶敏感性及凝血功能指标的相关性。方法 回顾性分析2019年1月—2021年2月全频下降型突发性耳聋患者48例,根据患者纤维蛋白原(FIB)的变化分为敏感组及非敏感组,检测患者凝血功能包括活化部分凝血活酶时间(APTT)、凝血酶原时间(PT)、凝血酶时间(TT)、FIB的变化及治疗前后纯音听阈变化。结果 ①48例患者总有效率为75.0%,其中平坦型总有效率为72.4%,全聋型总有效率为78.9%,敏感组有效率为85.7%,非敏感组有效率为60.0%,敏感组有效率高于非敏感组,差异具有统计学意义(P<0.05);②敏感组患者治疗后与治疗前相比FIB、APTT下降,TT、PT升高,差异具有统计学意义(P<0.05),非敏感组患者治疗后较治疗前FIB降低,TT升高,差异具有统计学意义(P<0.05)。治疗后,敏感组FIB低于非敏感组,TT、PT高于非敏感组,差异具有统计学意义(P<0.05)。结论 巴曲酶敏感性与临床治疗效果具有相关性,主要与FIB、PT、TT密切相关,与APTT相关性不大,但机体可能通过APTT内源性凝血功能,降低出血风险。巴曲酶可增强抗凝血功能,促进内耳微循环,使抗凝、纤溶和凝血在一定范围内保持平衡,安全性良好。  相似文献   
2.
目的探讨既往存在感音神经性听力损失突发性聋患者临床特征与疗效。方法对61例(63耳)既往存在感音神经性听力损失突发性聋患者的临床资料进行系统性分析,包括临床表现、疗效评估等,与同期收入院的既往不存在感音神经性听力损失突发性聋患者资料对比,分析发病和影响疗效的高危因素,总结该病发生、发展及预后的特点。结果既往存在和不存在感音神经性听力损失突聋患者的性别、现患耳侧别、病程差异无统计学意义(P值均>0.05),发病年龄差异具有统计学意义(P<0.05)。既往存在和不存在感音神经性听力损失突聋患者的听力曲线类型、听力损失程度差异无统计学意义(P值均>0.05),既往存在感音神经性听力损失突聋患者总有效率低于既往不存在感音神经性听力损失突聋患者总有效率,差异有显著统计学意义(χ2=6.915,P=0.009),既往存在感音神经性听力损失突聋患者痊愈率低于既往不存在感音神经性听力损失突聋患者痊愈率,差异无统计学意义(χ2=0.221,P=0.638)。结论既往存在感音神经性听力损失突聋患者病因复杂,疗效较差,应加大研究制定个性化的诊疗方案。  相似文献   
3.
目的观察银杏叶提取物注射液治疗突发性耳聋的有效性及药理作用分析。方法选取我院自2019年1月~2020年6月收治的突发性耳聋患者80例,随机分为实验组和对照组,每组40例。两组均进行常规治疗和辅助治疗,对照组采取静脉滴注丹参注射液联合低分子右旋糖酐氨基酸注射液治疗,实验组采取静脉银杏叶提取物注射液联合低分子右旋糖酐氨基酸注射液治疗。比较两组患者临床治疗效果和不良反应发生情况。结果经过治疗发现,实验组有效率97.5%,显著高于对照组82.5%,差异具有统计学意义(P<0.05)。实验组出现恶心呕吐不良反应仅1例,不良反应发生率为2.5%;对照组出现4例恶心呕吐、2例乏力以及2例头晕,不良反应发生概率为20.0%。实验组不良反应发生概率显著低于对照组,具有统计学意义(P<0.05)。结论突发性耳聋采用银杏叶提取物注射液治疗对提高治疗有效率有显著效果,并且不良反应发生概率低,值得临床推广使用。  相似文献   
4.
林国华针灸治疗难治性突发性耳聋经验撷要   总被引:2,自引:0,他引:2  
总结林国华教授针灸治疗难治性突发性耳聋经验,并对典型医案进行介绍。林国华教授认为本病多因少阳经气厥塞所致,提倡尽早针灸干预,治病求本,谨守"少阳暴厥"之病机,谨遵"疏解少阳,通耳开窍"之法,临证必用听宫,主取少阳经穴,辅予辨经取穴,巧施发蒙针法与气流灌耳法,妙用岭南火针疗法,必要时调气调神、加取募穴,共奏通耳复聪之效。  相似文献   
5.
目的确定东莞地区耳聋基因的变异类型和携带率。方法收集新生儿及门诊筛查的16182名个体,新生儿采集足跟血片,非新生儿采集外周静脉血样,对18个耳聋易感基因的100种变异进行检测。结果共检出1631例耳聋基因变异,总体检出率为10.08%,其中5例为纯合变异。SLC26A4基因变异的检出率最高(5.22%),共845例,其余依次为GJB2(673例,4.16%)、GJB3(100例,0.62%)、TMC1(12例,0.07%)、MYO15A(1例,0.01%)。GJB2基因c.235delC变异检出率最高(3.24%),共524例,其次为SLC26A4基因IVS7-2A>G变异(270例,1.67%)。33名个体(0.20%)同时携带两个变异,其中7例(0.04%)携带同一基因的复合杂合变异。结论扩大耳聋易感基因变异的筛查范围有助于了解携带情况及耳聋的遗传因素,对提早发现先天性耳聋、对受检者提供干预和遗传咨询具有重要的价值。  相似文献   
6.
Conclusion: Psychosocial factors should be considered during cochlear implantation (CI). There were differences in psychosocial characteristics according to the etiology of deafness. The outcomes may be affected by psychosocial variables such as the severity of mental distress and social problems as well as duration of deafness. Objective: To evaluate the psychosocial characteristics of deaf people undergoing CI and to determine which psychosocial factors affect performance after CI. Methods: A total of 289 subjects who underwent CI were enrolled. The participants were classified into prelingually deaf (pre-LD) and postlingually deaf groups (post-LD), including progressive and sudden deafness subgroups. The Minnesota Multiphasic Personality Inventory (MMPI) was administered before CI to measure psychosocial and emotional problems. To measure CI outcomes, speech perception ability was assessed by the open-set Korean version of the Central Institute of Deafness (K-CID) test and categories of auditory performance (CAP) scores before and after CI. Results: Approximately 45% of subjects experienced psychological problems before undergoing CI. Subjects in the Pre-LD group had more psychosocial distress and were more likely to be oversensitive in interpersonal situations, while those in the post-LD group were more depressed. Deafness duration and psychosocial factors significantly predicted hearing ability after CI. Deafness duration directly and indirectly affected the outcome of CI. That is, duration of deafness caused psychosocial problems, which may have resulted in negative effects on outcomes of CI.  相似文献   
7.
Hair cells of the inner ear, the mechanosensory receptors, convert sound waves into neural signals that are passed to the brain via the auditory nerve. Little is known about the molecular mechanisms that govern the development of hair cell–neuronal connections. We ascertained a family with autosomal recessive deafness associated with a common cavity inner ear malformation and auditory neuropathy. Via whole-exome sequencing, we identified a variant (c.2207G>C, p.R736T) in ROR1 (receptor tyrosine kinase-like orphan receptor 1), cosegregating with deafness in the family and absent in ethnicity-matched controls. ROR1 is a tyrosine kinase-like receptor localized at the plasma membrane. At the cellular level, the mutation prevents the protein from reaching the cellular membrane. In the presence of WNT5A, a known ROR1 ligand, the mutated ROR1 fails to activate NF-κB. Ror1 is expressed in the inner ear during development at embryonic and postnatal stages. We demonstrate that Ror1 mutant mice are severely deaf, with preserved otoacoustic emissions. Anatomically, mutant mice display malformed cochleae. Axons of spiral ganglion neurons show fasciculation defects. Type I neurons show impaired synapses with inner hair cells, and type II neurons display aberrant projections through the cochlear sensory epithelium. We conclude that Ror1 is crucial for spiral ganglion neurons to innervate auditory hair cells. Impairment of ROR1 function largely affects development of the inner ear and hearing in humans and mice.Sensorineural hearing loss (SNHL) is diagnosed in approximately 1 per 500 newborns (1). A genetic etiology is present in more than half of the cases. Inner ear anomalies (IEAs), demonstrated with computerized tomography or magnetic resonance imaging, are associated with SNHL in about one-third of individuals (2). Although IEAs can be diagnosed in patients with other clinical manifestations, such as those seen in Waardenburg [Mendelian Inheritance in Man (MIM) 193500], Pendred (MIM 274600), or BOR (MIM 113650) syndromes, the majority of cases fall into the category of nonsyndromic deafness. Despite recent progress in identifying genes that determine many forms of hearing loss (hereditaryhearingloss.org/), the genetic basis of IEAs in humans remains largely unknown.The inner ear is a complex organ that is built from a simple structure, referred to as the otocyst, through a series of morphogenetic events. Roughly, it consists of a dorsal vestibular and a ventral auditory component (3). Studies in model organisms have identified a number of genes that play roles in proper development of the inner ear. Mouse models have been particularly relevant because the anatomy and physiology of the murine auditory system are similar to those of humans. Mutations in human orthologs of many of these genes have been reported to cause deafness in humans as well (4).Next-generation sequencing technologies have allowed rapid identification of novel human deafness genes. Approximately 85% of disease-causing mutations in Mendelian disorders have been found in the protein-coding regions, despite the fact that this portion accounts for less than 2% of the entire human genome (5). Accordingly, whole exome sequencing (WES) has been frequently used because it allows for a targeted enrichment and resequencing of nearly all exons of protein-coding genes.In this study, via WES, we detected a mutation in ROR1 (receptor tyrosine kinase-like orphan receptor 1; MIM 602336), encoding receptor tyrosine kinase-like orphan receptor 1, that associates with an IEA and nonsyndromic deafness in a family. Further characterization of Ror1 mutant mice revealed that Ror1 deficiency results in defective hair cell innervation and abnormal cochlear development.  相似文献   
8.
目的:探讨不同听力曲线突发性耳聋患者的血液流变学改变情况及治疗效果。方法采集本院2010年3月~2011年10月收治的74例突发性耳聋患者的病史资料,所有患者给予血液流变学检测及治疗前后纯音测听,对所得结果进行统计学分析。结果1(平坦型组)、2组(高频下降型组)的全血黏度、血浆黏度差异无统计学意义(Q=0.53、0.08、0.42、0.00,P>0.05);1、2组的全血黏度、血浆黏度均高于3组(Q=3.97、4.25、3.47、4.58,P<0.05;Q=3.86、3.62、3.33、3.97,P<0.01)。1、2、3组的总有效率分别为57.14%、66.67%、100.00%,1、2组的治疗效果差异无统计学意义(χ2=0.48,P>0.05);1、2组的总有效率与3组比较,差异有统计学意义,3组的疗效优于1、2组(χ2=8.84、5.74,P<0.05)。结论听力曲线为平坦型及高频下降型的突发性耳聋患者,其全血黏度及血浆黏度高于低频下降型者。低频下降型组的治疗效果优于其余两组。  相似文献   
9.
目的:评估语前聋儿童人工耳蜗植入术后听觉言语能力的发展规律及其影响因素。方法对107例语前聋儿童人工耳蜗植入术后,应用婴幼儿有意义听觉整合量表(infant-toddler meaningful auditory integration scale/meaningful auditory integration scale ,IT -MAIS/MAIS)、听觉行为分级(categories of auditory performance , CAP)和言语可懂度分级(speech intelligibility rating ,SIR)三种问卷评估其听觉言发展水平,分析植入时间、植入年龄、实际年龄、术前助听器使用情况等对其的影响。结果107例语前聋儿童的植入年龄、植入时间对IT -M AIS/MAIS得分率有显著影响,植入时间、实际年龄对CAP、SIR分级有显著影响(P值均<0.05),而术前是否佩戴助听器对IT -MAIS/MAIS得分率、CAP、SIR分级均无显著影响(均为 P>0.05)。结论植入年龄、植入时间、实际年龄对语前聋儿童人工耳蜗植入后的听觉言语能力发展有显著影响,而术前是否佩戴助听器对其听觉言语能力的影响有待后续研究证实。  相似文献   
10.
Hypoparathyroidism, deafness, and renal dysplasia (HDR; OMIM 146255) syndrome is a rare disease, inherited dominantly and found to be related with GATA3 (GATA binding protein 3) gene mutations. A 13-year and 8-month-old boy who presented with hypocalcemia was diagnosed with hypoparathyroidism. He also had dysmorphic facial features, renal anomaly (pelvic kidney), and mild sensorineural hearing loss. His cranial computed tomography revealed multiple calcifications in bilateral centrum semiovale, corona radiata, and basal ganglions suggesting a persistent hypoparathyroidism. Thus, the presence of triad of HDR syndrome was considered, and genetic analysis using a next-generation sequencer identified a novel de novo missense mutation in exon 4 p.R276Q (c.827G>A) of GATA3 gene. This is the second patient who was reported to have a mutation in GATA3 gene from Turkey. In conclusion, although HDR syndrome is a rare condition, it should be kept in mind in patients with hypoparathyroidism. Classical triad can easily be identified if patients diagnosed with hypoparathyroidism are also evaluated with a urinary tract ultrasound and an audiometer.  相似文献   
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