全文获取类型
收费全文 | 5795篇 |
免费 | 509篇 |
国内免费 | 148篇 |
专业分类
耳鼻咽喉 | 39篇 |
儿科学 | 165篇 |
妇产科学 | 76篇 |
基础医学 | 1358篇 |
口腔科学 | 97篇 |
临床医学 | 573篇 |
内科学 | 966篇 |
皮肤病学 | 87篇 |
神经病学 | 418篇 |
特种医学 | 213篇 |
外科学 | 472篇 |
综合类 | 438篇 |
预防医学 | 632篇 |
眼科学 | 85篇 |
药学 | 390篇 |
中国医学 | 168篇 |
肿瘤学 | 275篇 |
出版年
2023年 | 98篇 |
2022年 | 128篇 |
2021年 | 264篇 |
2020年 | 258篇 |
2019年 | 249篇 |
2018年 | 209篇 |
2017年 | 235篇 |
2016年 | 196篇 |
2015年 | 236篇 |
2014年 | 377篇 |
2013年 | 445篇 |
2012年 | 290篇 |
2011年 | 343篇 |
2010年 | 244篇 |
2009年 | 306篇 |
2008年 | 270篇 |
2007年 | 256篇 |
2006年 | 198篇 |
2005年 | 170篇 |
2004年 | 172篇 |
2003年 | 130篇 |
2002年 | 135篇 |
2001年 | 133篇 |
2000年 | 85篇 |
1999年 | 91篇 |
1998年 | 80篇 |
1997年 | 74篇 |
1996年 | 57篇 |
1995年 | 61篇 |
1994年 | 66篇 |
1993年 | 53篇 |
1992年 | 58篇 |
1991年 | 35篇 |
1990年 | 48篇 |
1989年 | 39篇 |
1988年 | 36篇 |
1987年 | 29篇 |
1986年 | 28篇 |
1985年 | 48篇 |
1984年 | 42篇 |
1983年 | 24篇 |
1982年 | 33篇 |
1981年 | 24篇 |
1980年 | 19篇 |
1979年 | 13篇 |
1978年 | 14篇 |
1977年 | 10篇 |
1976年 | 12篇 |
1975年 | 5篇 |
1974年 | 5篇 |
排序方式: 共有6452条查询结果,搜索用时 15 毫秒
1.
2.
C. Vogrig J.-S. Louis F. Avila R. Gillet G. Hossu A. Blum-Moyse P.A. Gondim Teixeira 《Diagnostic and interventional imaging》2021,102(3):181-187
PurposeThe purpose of this study was to compare morphologic assessment and relaxometry of patellar hyaline cartilage between conventional sequences (fast spin-echo [FSE] T2-weighted fat-saturated and T2-mapping) and synthetic T2 short-TI inversion recovery (STIR) and T2 maps at 1.5 T magnetic resonance imaging (MRI).MethodThe MRI examinations of the knee obtained at 1.5 T in 49 consecutive patients were retrospectively studied. There were 21 men and 28 women with a mean age of 45 ± 17.7 (SD) years (range: 18–88 years). Conventional and synthetic acquisitions were performed, including T2-weighted fat-saturated and T2-mapping sequences. Two radiologists independently compared patellar cartilage T2-relaxation time on conventional T2-mapping and synthetic T2-mapping images. A third radiologist evaluated the patellar cartilage morphology on conventional and synthetic T2-weighted images. The presence of artifacts was also assessed. Interobserver agreement for quantitative variables was assessed using intraclass correlation coefficient (ICC).ResultsIn vitro, conventional and synthetic T2 maps yielded similar mean T2 values 58.5 ± 2.3 (SD) ms and 58.8 ± 2.6 (SD) ms, respectively (P = 0.414) and 6% lower than the expected experimental values (P = 0.038). Synthetic images allowed for a 15% reduction in examination time compared to conventional images. On conventional sequences, patellar chondropathy was identified in 35 patients (35/49; 71%) with a mean chondropathy grade of 4.8 ± 4.8 (SD). On synthetic images, 28 patients (28/49; 57%) were diagnosed with patellar chondropathy, with a significant 14% difference (P = 0.009) and lower chondropathy scores (3.7 ± 4.9 [SD]) compared to conventional images. Motion artifacts were more frequently observed on synthetic images (18%) than on conventional ones (6%). The interobserver agreement was excellent for both conventional and synthetic T2 maps (ICC > 0.83). Mean cartilage T2 values were significantly greater on synthetic images (36.2 ± 3.8 [SD] ms; range: 29-46 ms) relative to conventional T2 maps (31.8 ± 4.1 [SD] ms; range: 26-49 ms) (P < 0.0001).ConclusionDespite a decrease in examination duration, synthetic images convey lower diagnostic performance for chondropathy, greater prevalence of motion artifacts, and an overestimation of T2 values compared to conventional MRI sequences. 相似文献
3.
刘光 ' target='_blank'> 刘支娜 ' target='_blank'> 张玲 ' target='_blank'> 王会瑟 ' target='_blank'> 蔺颐 ' target='_blank'> 张亚涛 ' target='_blank'> 陶金 ' target='_blank'> 刘闯 ' target='_blank'> 《现代肿瘤医学》2021,(2):323-326
目的:探讨基于脉压变异度(PPV)的目标导向液体治疗(GDFT)在腹膜后巨大恶性肿瘤切除术患儿中的应用。方法:择期行腹膜后巨大恶性肿瘤切除术患儿64例,年龄0.5~3岁,ASA Ⅱ-Ⅲ级。随机将患儿分为目标导向液体治疗组(G组)和常规液体治疗组(C组),每组32例。G组以PPV为指导,根据GDFT方案进行液体管理,C组采用常规液体管理。记录手术开始(T1)、手术开始后1 h(T2)、手术结束(T3)的MAP、CVP、PPV、Lac值、TNF-α、IL-6浓度。记录术中输注晶体液量、胶体液量、液体总量、出血量、尿量、手术时间、多巴胺使用率以及排气时间、术后住院时间和恶心呕吐发生率。结果:G组输注晶体液量显著少于C组(P<0.05),而输注胶体液量显著多于C组(P<0.05)。两组术中输注液体总量、出血量、尿量与多巴胺使用率方面差异无统计学意义。T2、T3时刻,G组PPV、TNF-α、IL-6显著低于C组(P<0.05),而两组间MAP、CVP、Lac在各时点差异无统计学意义。G组术后排气时间明显短于C组(P<0.05),而在术后恶心呕吐发生率和住院时间方面两组差异无统计学意义。结论:PPV指导的GDFT可以应用于腹膜后巨大恶性肿瘤切除术患儿,能维持其血流动力学稳定,减少炎症因子IL-6、TNF-α释放,促进胃肠功能恢复,但对术后转归无明显影响。 相似文献
4.
《Clinical neurophysiology》2021,132(2):315-322
ObjectivePrevious studies have demonstrated voluntary movement alterations as well as motor cortex excitability and plasticity changes in patients with mild cognitive impairment (MCI). To investigate the pathophysiology of movement abnormalities in MCI, we tested possible relationships between movement abnormalities and primary motor cortex alterations in patients.MethodsFourteen amnestic MCI (aMCI) patients and 16 healthy controls were studied. Cognitive assessment was performed using clinical scales. Finger tapping was recorded by a motion analysis system. Transcranial magnetic stimulation was used to test the input/output curve of motor evoked potentials, intracortical inhibition, and short-latency afferent inhibition. Primary motor cortex plasticity was probed by theta burst stimulation. We investigated correlations between movement abnormalities, clinical scores, and cortical neurophysiological parameters.ResultsMCI patients showed less rhythmic movement but no other movement abnormalities. Cortical excitability measures were normal in patients, whereas plasticity was reduced. Movement rhythm abnormalities correlated with frontal dysfunction scores.ConclusionOur study in MCI patients demonstrated abnormal voluntary movement and plasticity changes, with no correlation between the two. Altered rhythm correlated with frontal dysfunction.SignificanceOur results contribute to the understanding of pathophysiological mechanisms of motor impairment in MCI. 相似文献
5.
目的比较基因组拷贝数变异测序(CNV-seq)技术和染色体核型分析和在产前胎儿遗传学诊断中的应用价值。方法收集来我院有产前诊断指征进行羊水穿刺的259例孕妇,取材后,送检染色体核型分析和CNV-seq,比较两种方法在产前诊断中的优缺点。结果259例标本中,共诊断异常染色体核型及微缺失微重复23例,总阳性诊断率8.88%(23/259),CNV-seq结果显示,共有22例染色体拷贝数异常(12例三体+9例微缺失微重复+1例三倍体),检出率为8.49%;染色体核型分析结果显示为:17例染色体异常(12例三体+3例结构异常+1例嵌合型+1例三倍体),检出率为6.56%。此外还检出染色体多态7例。结论CNV-seq与染色体核型分析对于染色体非整倍体的检测效力一致,CNV-seq能检测染色体微缺失微重复,染色体核型分析则能诊断出三体具体核型,在怀疑性染色体异常时,建议行两者联合检测。 相似文献
6.
《Obesity research & clinical practice》2022,16(5):400-406
AimThe current pediatric obesity health challenge necessitates a better understanding of the factors affecting weight loss success during interventions. The aim of this observational study was to test the impact of the rate of initial weight loss and body weight variability on weight loss during a 9-month residential, multidisciplinary weight loss program in adolescents with obesity.MethodsThis retrospective study considered a whole sample of 510 adolescents with obesity (12–16 years, 435 girls). Body weight assessment was performed before (T0) and each week during the 9 months of a multidisciplinary weight loss program. Initial weight change (week 4-W4) and overall weight change at week 12 (T1) and the end of the intervention (T2) were considered. Participants were divided into three groups (tertiles), based on their percentage of weight loss between T0 and W4; and weight variability was expressed by the root mean square error (RMSE) around each participant’s regression line at each considered period (W4, T1, T2).ResultsAdolescents with lower initial weight loss at W4 (tertile 3) displayed the lesser weight loss at T1 and T2 compared with adolescents in tertile 1 and 2. The RMSE was positively associated with the percentage of weight loss of the period considered, but when the analyses were adjusted for age and initial body weight, there was no more significant association.ConclusionsThe rate of weight loss during the first few weeks is crucial for weight loss success, and weight variability is positively associated with weight loss in adolescents with obesity. Overall, results show that initial body weight is a determinant characteristic to consider during a lifestyle intervention. Further studies are thus needed to better understand the relationship between body weight change patterns and weight loss during the dynamic state that is adolescence. 相似文献
7.
Karis Bennett Tanner Vincent Sumathilatha Sakthi-Velavan 《Clinical anatomy (New York, N.Y.)》2022,35(1):52-64
The patellar ligament (PL) is an epiphyseal ligament and is part of the extensor complex of the knee. The ligament has gained attention due to its clinical relevance to autograft and tendinopathy. A variety of anatomical variations of the PL such as aplasia, numerical variations, and vascularity are being reported recently by clinicians and anatomists. The aim of this literature was to review the available literature to provide a consensus regarding anatomic variations of the PL, neurovasculature surrounding the PL, histology of the PL, and various aspects of PL measurements with relevance to the surgical considerations and sex and age-related differences. A narrative review of the patellar ligament was performed by conducting a detailed literature search and review of relevant articles. A total of 90 articles on the patellar ligament were included and were categorized into studies based on anatomical variations, neurovasculature, morphometrics, microanatomy, sex and age-related difference, and ACL reconstruction. The anatomical variations and morphometrics of the PL were found to correlate with the frequency of strain injuries, tendinopathy, and efficacy of the PL autograft in anterior cruciate ligament reconstruction. The sex differences in PL measurements and the effect of estrogen on collagen synthesis explained a higher incidence of patellar tendinopathy in women. An awareness of its variations enables careful selection of surgical incisions, thereby avoiding complications related to nerve injury. Accurate knowledge of the PL microanatomy assists in understanding the mechanism of ligament degeneration, rupture, autograft harvesting, and ligamentization results. 相似文献
8.
Beom Jun Kim Hye-young Wang Hyeyoung Lee So-Yeon Lee Soo-Jong Hong Eung Ho Choi 《ANNALS OF DERMATOLOGY》2019,31(3):286
BackgroundHereditary factors contribute to atopic dermatitis (AD) development. We developed the reverse blot hybridization assay (REBA) kit to simultaneously detect variations in skin barrier- and immune response-related genes prevalent in Korean AD patients.ObjectiveTo identify genetic variations and clinical characteristics that could predict early AD development.MethodsWe compared AD-related genetic variations between early-onset AD subjects and non-AD controls, and clinical characteristics and genetic variations between early- and late-onset AD subjects. We compared 28 early-onset AD subjects and 57 non-AD controls from a birth cohort and 108 early- (age ≤3 years) and 90 late-onset AD subjects and 189 non-AD controls from a university hospital. Genetic variations were detected via REBA.ResultsThere were no differences in AD-related genetic variation between early-onset AD subjects and non-AD controls in the birth cohort. When the birth cohort and hospital populations were combined, early-onset AD subjects and non-AD controls showed different frequencies of genetic variations of KLK7, SPINK5 1156, DEFB1, IL5RA, IL12RB1a, and IL12RB1b. No differences in the frequency of genetic variations were observed between early- and late-onset AD subjects. Immunoglobulin E positivity for house dust mites was prevalent in late-onset AD subjects. A family history of atopic diseases was associated with early-onset AD.ConclusionNo AD-related genetic variations could predict early AD development in Koreans, even though neonates with a family history of atopic diseases are likely to develop AD at ≤3 years of age. Environmental exposure may be more important than genetic variation in determining the onset age of AD. 相似文献
9.
10.
目的:探讨性别和年龄因素对电离辐射诱导的离体人外周血中辐射敏感基因mRNA表达变化的影响。方法:采集30例健康人离体外周血,以剂量率为1 Gy/min的60Co γ射线进行照射,照射剂量分别为0.5、1、2、3、4、6和8 Gy (以0 Gy为阴性对照组),照射后培养12 h,应用实时荧光定量PCR (qPCR)方法检测18个辐射敏感基因的mRNA表达水平变化,分析性别和年龄因素对这些基因mRNA表达水平的影响。结果:与阴性对照组相比,各剂量γ射线照射组人外周血18个辐射敏感基因的mRNA表达水平均明显增加,并且呈剂量-效应关系(R2=0.63~0.97,P < 0.05)。在相同照射剂量,MDM2、XPC、FDXR、DDB2、ASTN2和TNFSF4 mRNA相对表达水平在不同个体之间存在较大的差异。女性外周血中BAX、TNFRSF10B、ASTN2、TNFSF4、POLH和GADD45A mRNA相对表达水平均高于男性,在0.5~8 Gy照射剂量范围内具有统计学差异(P < 0.05或P < 0.01)。MDM2、FDXR、DDB2和RPS27L mRNA表达水平在不同年龄组间(20~29岁、30~39岁、40~49岁和50~60岁)存在差异(P < 0.05或P < 0.01)。结论:离体人外周血中辐射敏感基因mRNA表达水平的变化存在个体间差异,且与受照者性别和年龄相关。 相似文献