全文获取类型
收费全文 | 2615篇 |
免费 | 194篇 |
国内免费 | 7篇 |
专业分类
耳鼻咽喉 | 21篇 |
儿科学 | 107篇 |
妇产科学 | 31篇 |
基础医学 | 286篇 |
口腔科学 | 50篇 |
临床医学 | 210篇 |
内科学 | 711篇 |
皮肤病学 | 75篇 |
神经病学 | 141篇 |
特种医学 | 119篇 |
外科学 | 392篇 |
综合类 | 100篇 |
一般理论 | 1篇 |
预防医学 | 135篇 |
眼科学 | 55篇 |
药学 | 207篇 |
中国医学 | 12篇 |
肿瘤学 | 163篇 |
出版年
2022年 | 19篇 |
2021年 | 52篇 |
2020年 | 24篇 |
2019年 | 41篇 |
2018年 | 42篇 |
2017年 | 39篇 |
2016年 | 49篇 |
2015年 | 55篇 |
2014年 | 60篇 |
2013年 | 79篇 |
2012年 | 122篇 |
2011年 | 152篇 |
2010年 | 71篇 |
2009年 | 78篇 |
2008年 | 98篇 |
2007年 | 111篇 |
2006年 | 104篇 |
2005年 | 97篇 |
2004年 | 92篇 |
2003年 | 69篇 |
2002年 | 62篇 |
2001年 | 58篇 |
2000年 | 81篇 |
1999年 | 53篇 |
1998年 | 34篇 |
1997年 | 31篇 |
1996年 | 23篇 |
1995年 | 26篇 |
1994年 | 17篇 |
1992年 | 80篇 |
1991年 | 39篇 |
1990年 | 53篇 |
1989年 | 39篇 |
1988年 | 47篇 |
1987年 | 45篇 |
1986年 | 36篇 |
1985年 | 37篇 |
1984年 | 27篇 |
1983年 | 17篇 |
1982年 | 18篇 |
1979年 | 41篇 |
1978年 | 24篇 |
1977年 | 26篇 |
1975年 | 23篇 |
1974年 | 26篇 |
1973年 | 37篇 |
1972年 | 32篇 |
1971年 | 22篇 |
1970年 | 20篇 |
1935年 | 16篇 |
排序方式: 共有2816条查询结果,搜索用时 15 毫秒
101.
Nishtha Gadkari Shilpa Bawane Ratima Chopra Kalyani Bhate Deepak Kulkarni 《Journal of cranio-maxillo-facial surgery》2019,47(10):1542-1550
BackgroundThe zygomaticomaxillary complex (ZMC) functions as the main buttress for the lateral portion of the middle third of the facial skeleton and because of its prominent position & convex shape, it is frequently fractured, alone or along with other bones of the midface. The management of the ZMC fractures is debatable as the literature is saturated with various theories. A number of techniques, from closed reduction to open reduction and internal fixation can be effectively used to manage these fractures. Controversies lie right from the amount of fixation (1-, 2-, 3- or 4- point fixation) required to the ideal approach, and there is no conclusive view on its ideal line of management.ObjectiveTo compare Malar asymmetry after 2-point vs 3-point fixation in the treatment of zygomaticomaxillary complex fractures.Data sourceElectronic search of Pub Med, Google Scholar, Institutional Library, Email to authors and manual search of various journals.Study eligibility criteriaThe following criteria were used to select the studies on 2- point and 3-point fixation methods in Zygomaticomaxillary complex fractures. Inclusion criteria had articles that included clinical studies published in the English language or those having sufficient data in English on 2-point or 3-point fixation in the treatment of zygomaticomaxillary complex fractures between the period of 1st January 2008 to 30th September 2018. While exclusion criteria were articles not published in the English language before 1st January 2008 and after 30th September 2018, any reviews, abstracts, letters to editors, editorials and in vitro studies were excluded. Studies that included patients with craniofacial and secondary deformities were also excluded.InterventionOpen reduction and internal fixation using 2-point and 3-point fixation methods in the treatment of Zygomaticomaxillary complex fractures.ResultsPreliminary screening consisted of 757 studies and additional records identified through other sources of 272 studies. Amongst these 1029 studies, 837 studies were excluded after reviewing the titles. A review of abstract further excluded 71 studies, so 34 studies that remained were evaluated to fit the eligibility criteria. On the basis of information on fixation methods and parameters of evaluation of fixation method, 26 studies were further excluded. Thus 8 studies with a total of 823 estimates were included in qualitative synthesis.LimitationsParameters assessed by all the authors varied and hence a standardisation for comparison could not be done.ConclusionFive out of eight studies showed that the use of 3-point fixation in the treatment of zygomaticomaxillary complex fractures was superior than 2-point fixation for the same. Hence it can be concluded that 3-point fixation is superior than 2-point fixation in reducing malar asymmetry in zygomaticomaxillary complex fractures.Future implicationsFuture studies with uniform parameters being assessed can be done. 3-point fixation can be used as a standard treatment modality in the effective management of Zygomaticomaxillary complex fractures. 相似文献
102.
103.
104.
105.
106.
We report, to the best of our knowledge the first case of prosthetic mitral valve mucormycosis caused by Mucor species in an 18-year-old female after mitral valve replacement. She was successfully treated with surgery and antifungal treatment. Mucormycosis was documented by direct demonstration, isolation and histopathological findings of the fungus from embolus and prosthetic mitral valve thrombus. 相似文献
107.
Christopher T. Gordon Maya Chopra Myriam Oufadem Olivier Alibeu Marc Bras Nathalie Boddaert Christine Bole‐Feysot Patrick Nitschké Véronique Abadie Stanislas Lyonnet Jeanne Amiel 《American journal of medical genetics. Part A》2018,176(1):181-186
We report two unrelated patients with Pierre Robin sequence (PRS) and a strikingly similar combination of associated features. Whole exome sequencing was performed for both patients. No single gene containing likely pathogenic point mutations in both patients could be identified, but the finding of an essential splice site mutation in mediator complex subunit 13 like (MED13L) in one patient prompted the investigation of copy number variants in MED13L in the other, leading to the identification of an intragenic deletion. Disruption of MED13L, encoding a component of the Mediator complex, is increasingly recognized as the cause of an intellectual disability syndrome with associated facial dysmorphism. Our findings suggest that MED13L–related disorders are a possible differential diagnosis for syndromic PRS. 相似文献
108.
Izak J. Bisschoff Christine Zeschnigk Denise Horn Brigitte Wellek Angelika Rieß Maja Wessels Patrick Willems Peter Jensen Andreas Busche Jens Bekkebraten Maya Chopra Hanne Dahlgaard Hove Christina Evers Ketil Heimdal Ann‐Sophie Kaiser Erdmut Kunstmann Kristina Lagerstedt Robinson Maja Linné Patricia Martin James McGrath Winnie Pradel Katrina E. Prescott Bernd Roesler Gorazd Rudolf Ulrike Siebers‐Renelt Nataliya Tyshchenko Dagmar Wieczorek Gerhard Wolff William B. Dobyns Deborah J. Morris‐Rosendahl 《Human mutation》2013,34(1):237-247
OFD1, now recognized as a ciliopathy, is characterized by malformations of the face, oral cavity and digits, and is transmitted as an X‐linked condition with lethality in males. Mutations in OFD1 also cause X‐linked Joubert syndrome (JBTS10) and Simpson–Golabi–Behmel syndrome type 2 (SGBS2). We have studied 55 sporadic and six familial cases of suspected OFD1. Comprehensive mutation analysis in OFD1 revealed mutations in 37 female patients from 30 families; 22 mutations have not been previously described including two heterozygous deletions spanning OFD1 and neighbouring genes. Analysis of clinical findings in patients with mutations revealed that oral features are the most reliable diagnostic criteria. A first, detailed evaluation of brain MRIs from seven patients with cognitive defects illustrated extensive variability with the complete brain phenotype consisting of complete agenesis of the corpus callosum, large single or multiple interhemispheric cysts, striking cortical infolding of gyri, ventriculomegaly, mild molar tooth malformation and moderate to severe cerebellar vermis hypoplasia. Although the OFD1 gene apparently escapes X‐inactivation, skewed inactivation was observed in seven of 14 patients. The direction of skewing did not correlate with disease severity, reinforcing the hypothesis that additional factors contribute to the extensive intrafamilial variability. 相似文献
109.
Myocarditis manifesting as persistent atrial standstill 总被引:2,自引:0,他引:2
Persistent atrial standstill complicating inflammatory myocarditis in a young boy is presented. The disease was marked by a stuttering course characterized by intermittent return of atrial rhythm in the form of atrial flutter and fibrillation until persistent standstill lasting till the last follow-up occurred. The relevant literature is reviewed. 相似文献
110.
Nehal E. Elsadek Abdalrazeq Nagah Tarek M. Ibrahim Hitesh Chopra Ghada A. Ghonaim Sherif E. Emam Simona Cavalu Mohamed S. Attia 《Materials》2022,15(5)
Electrospinning (ES) has become a straightforward and customizable drug delivery technique for fabricating drug-loaded nanofibers (NFs) using various biodegradable and non-biodegradable polymers. One of NF’s pros is to provide a controlled drug release through managing the NF structure by changing the spinneret type and nature of the used polymer. Electrospun NFs are employed as implants in several applications including, cancer therapy, microbial infections, and regenerative medicine. These implants facilitate a unique local delivery of chemotherapy because of their high loading capability, wide surface area, and cost-effectiveness. Multi-drug combination, magnetic, thermal, and gene therapies are promising strategies for improving chemotherapeutic efficiency. In addition, implants are recognized as an effective antimicrobial drug delivery system overriding drawbacks of traditional antibiotic administration routes such as their bioavailability and dosage levels. Recently, a sophisticated strategy has emerged for wound healing by producing biomimetic nanofibrous materials with clinically relevant properties and desirable loading capability with regenerative agents. Electrospun NFs have proposed unique solutions, including pelvic organ prolapse treatment, viable alternatives to surgical operations, and dental tissue regeneration. Conventional ES setups include difficult-assembled mega-sized equipment producing bulky matrices with inadequate stability and storage. Lately, there has become an increasing need for portable ES devices using completely available off-shelf materials to yield highly-efficient NFs for dressing wounds and rapid hemostasis. This review covers recent updates on electrospun NFs in nanomedicine applications. ES of biopolymers and drugs is discussed regarding their current scope and future outlook. 相似文献