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791.
792.
FU XI ZHAO~ YA QIN MU~ JUN CHENG GUO~ RUN HUA LIU~~ Microbiological Lab ~Surgery Lab Medical College of Datong University Datong P. R. China 《中华微生物学和免疫学杂志(英文版)》2005,3(4):246-253
Carcinomaofthecervixisthesecondleading causeofdeathamongwomenworldwide.Each year,anestimated500000casesarenewlydiag nosed[1].Manystudiesshowedinfectionofhu manpapillomavirus(HPV)wasoneofthemost importantetiologicfactorsforcervicalcarcinoma[24].Morethan95%ofallcervicalcarcinomas havebeenfoundtobeassociatedwithHPV(ma inlytypes16and18)[5].Thestudiesinmolec ularoncologyrecentlyshowedthatitresultedin occurrenceanddevelopmentofcervicalcarcinomasthatcarcinogenicfactorsmadeproto oncogene activatean… 相似文献
793.
PE Cohn-Hokke MW Elting YA Pijnenburg JC van Swieten 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2012,(6):628-643
With increased frequency, clinical geneticists are asked for genetic advice on the heredity of dementia in families. Alzheimer's disease is in most cases a complex disease, but may be autosomal dominant inherited. Mutations in the PSEN1 gene are the most common genetic cause of early onset Alzheimer's disease, whereas APP and PSEN2 gene mutations are less frequent. Familial frontotemporal dementia may be associated with a mutation in the MAPT or GRN gene, or with a repeat expansion in the C9orf72 gene. All these genes show autosomal dominant inheritance with a high penetrance. Although Alzheimer's disease and frontotemporal dementia are clinically distinguishable entities, phenotypical overlap may occur. Rarely, dementia is caused by mutations in other autosomal dominant genes or by genetic defects with autosomal recessive, X-linked dominant or mitochondrial inheritance. The inherited forms of frontotemporal dementia and Alzheimer's disease show a large phenotypic variability also within families, resulting in many remaining uncertainties for mutation carriers. Therefore, genetic counseling before performing genetic testing is essential in both symptomatic individuals and healthy at risk relatives. This review provides an overview of the genetic causes of dementia and discusses all aspects relevant for genetic counseling and testing. Furthermore, based on current knowledge, we provide algorithms for genetic testing in patients with early onset Alzheimer's disease or frontotemporal dementia. ? 2012 Wiley Periodicals, Inc. 相似文献
794.
795.
目的:检测口腔鳞癌组织(OSCC)中NBS1的表达水平,探讨其与OSCC病理分化级别的相关性以及在肿瘤发生发展中的作用。方法:①采用免疫组化(SP法)检测NBS1蛋白在30例口腔鳞癌组织、9例癌旁组织中的表达。②应用RT-PCR技术检测组织中NBS1的mRNA表达水平。结果:在OSCC与癌旁正常组织中,NBS1 mRNA和蛋白表达差异显著,在口腔癌组织中均表达较高,并随着病理级别增高而增高(P<0.05)。结论:NBS1在不同病理分化程度OSCC中表达水平的差别与多种因素密切相关,与肿瘤的恶性生物学行为有关,其表达水平可成为判断口腔鳞癌侵袭转移和预后的指标之一。 相似文献
796.
Background
Although attention to human rights in Indonesia has been improving over the past decade, the human rights situation of persons with mental disorders is still far from satisfactory. The purpose of this paper is to examine the legal framework for protection of human rights of persons with mental disorder and the extent to which Indonesia's international obligations concerning the right to health are being met. 相似文献797.
Mami Tamai Atsushi Kawakami Masataka Uetani Shoichiro Takao Kazuhiko Arima Naoki Iwamoto Keita Fujikawa Toshiyuki Aramaki Shin‐YA Kawashiri Kunihiro Ichinose Makoto Kamachi Hideki Nakamura Tomoki Origuchi Hiroaki Ida Kiyoshi Aoyagi Katsumi Eguchi 《Arthritis care & research》2009,61(6):772-778
Objective
To evaluate whether magnetic resonance imaging (MRI) of the wrists and finger joints and an analysis of serologic autoantibodies are clinically meaningful for the subsequent development of rheumatoid arthritis (RA) in patients with undifferentiated arthritis (UA).Methods
A total of 129 patients with UA, a disease status formally confirmed by a rheumatologist over a period of at least 1 year, were included. Gadolinium‐diethylenetriamine–enhanced MRI of both wrists and finger joints and serologic variables were examined upon admission to our Early Arthritis Clinic at Nagasaki University. After a prospective followup of 1 year, a predictive value for the development of RA was determined for each patient.Results
The subjects were evaluated for their positive or negative status with respect to 3 objective measures at study entry: anti–cyclic citrullinated peptide (anti‐CCP) antibodies and/or IgM‐rheumatoid factor, MRI‐proven symmetric synovitis, and MRI‐proven bone edema and/or bone erosion. The patients who were positive for at least 2 of these measures progressed to RA at 1 year with a 79.7% positive predictive value (PPV), 63.0% negative predictive value, 75.9% specificity, 68.0% sensitivity, and 71.3% accuracy. Furthermore, in 22 UA patients positive for both anti‐CCP antibodies and MRI‐proven bone edema who were considered to have progressed to RA at 1 year, the PPV was increased to 100%. A close correlation was found between the present rule and that established in the Leiden Early Arthritis Cohort.Conclusion
MRI‐proven early joint damage in conjunction with serologic autoantibodies is efficient in predicting progression from UA to RA. This method can be used to identify patients who would benefit from early treatment with disease‐modifying antirheumatic drugs. 相似文献798.
WAN‐TZU CHEN WEN‐CHUN HUNG WAN‐YI KANG YA‐CHUN HUANG YUE‐CHIU SU CHING‐HSIU YANG CHEE‐YIN CHAI 《APMIS : acta pathologica, microbiologica, et immunologica Scandinavica》2009,117(3):176-184
This study examines whether the expression of cyclooxgenase‐2 (COX‐2) in urothelial carcinoma (UC) is associated with macrophage infiltration, hypoxia‐inducible factor‐1α (HIF‐1α) expression and angiogenesis. We investigated the expression of COX‐2 associated with HIF‐1α and performed double immunohistochemical analysis of 216 UCs for COX‐2 expression and the correlation with tumor‐associated‐macrophage (TAM) density and microvessel density (MVD) in situ. A high expression of COX‐2 was positively correlated with tumor invasiveness, histologic grade and HIF‐1α expression in UC (p<0.0001, p=0.003, p<0.0001, respectively). Quantification of double staining of COX‐2/CD34 and COX‐2/CD68 showed that a higher MVD and TAM density was found in COX‐2 high‐expression than in COX‐2 low‐expression tumor fields (p<0.0001). Adjacent to the principal of COX‐2 expression areas, MVD value and TAM density were significantly increased in HIF‐1α high‐expression specimens compared with HIF‐1α low‐expression ones (p<0.0001). Interestingly, our data revealed that high COX‐2 expression (p=0.002), high HIF‐1α expression (p<0.0001) and TAM density (p<0.0001) were all associated with high MVD value. Our results suggest that COX‐2 may produce a cooperative effect in promoting tumor progression and may be involved in the process of angiogenesis through increasing TAM infiltration or HIF‐1α regulation by hypoxia. 相似文献
799.
血管平滑肌脂肪瘤(Angiomyolipoma,AML)是一种少见的主要好发于肾脏的间叶肿瘤.肾外AML偶见于肝脏、腹膜后、纵隔等处[1].发生于小肠系膜的AML午见.现将我院经于术病理证实的1例小肠系膜AML报告如下.病例男,20岁,发现腹部肿块3,中余入院.查体:神清、精神可,心肺(一).腹平软,左侧腹部以脐为中心可触及一约15cm人小的肿块,质韧界清,活动度大,无压痛,移动性浊音(一),神经系统(一).T 36.7 ℃,P 80次/min,R 18次/min,血压120/85mmHg.血尿常规与肝功能生化检查末见异常. 相似文献
800.
EEG synchronization likelihood in mild cognitive impairment and Alzheimer's disease during a working memory task. 总被引:6,自引:0,他引:6
Y A L Pijnenburg Y v d Made A M van Cappellen van Walsum D L Knol Ph Scheltens C J Stam 《Clinical neurophysiology》2004,115(6):1332-1339
OBJECTIVE: Synchronization likelihood analysis of resting state EEG has shown that cognitive dysfunction in Alzheimer's disease (AD) and its precursor mild cognitive impairment (MCI) are associated with a loss of functional connectivity in high (upper alpha and beta) frequency bands. Working memory tasks are known to change functional connectivity, but it is unknown whether this increases the differences between AD, MCI and healthy controls. Our objective was to investigate the behavior of synchronization likelihood of multichannel EEG in AD, MCI and cognitively healthy controls, both at rest and during a working memory task. METHODS: EEGs (200 Hz sample frequency, 21 channels, average reference) were recorded at rest as well as during a visual working memory task in 14 patients with AD according to the NINCDS-ADRDA criteria (mean age 76.4; SD 13.6), 11 patients with MCI according to the criteria of Petersen (mean age 78.4; SD 6.4) and 14 with subjective memory complaints but no demonstrable memory disturbance (mean age 61.6; SD 26.6). The synchronization likelihood was computed over 19 channels, comparing each channel with all the other channels for the 0.5-4, 4-8, 8-10, 10-12, 12-30, 30-50 Hz frequency bands. RESULTS: The synchronization likelihood was significantly decreased in the upper alpha (10-12) and beta (12-30) bands in AD compared to persons with subjective memory complaints. The working memory task scores strongly correlated with Mini-Mental State Examination scores. During the working memory task the synchronization likelihood was significantly higher in MCI compared to the control subjects in the lower alpha band (8-10 Hz). CONCLUSIONS: Decrease of beta band synchronization occurs in mild AD, both in a resting condition and during a working memory task. SIGNIFICANCE: Decrease of beta band synchronization in mild AD is a robust finding. The present study confirms our findings in a different cohort of patients, using alternative frequency bands. The diagnostic value of the synchronization likelihood in AD and MCI needs to be further established. 相似文献