全文获取类型
收费全文 | 1937篇 |
免费 | 115篇 |
国内免费 | 5篇 |
专业分类
耳鼻咽喉 | 38篇 |
儿科学 | 46篇 |
妇产科学 | 29篇 |
基础医学 | 261篇 |
口腔科学 | 169篇 |
临床医学 | 146篇 |
内科学 | 394篇 |
皮肤病学 | 58篇 |
神经病学 | 226篇 |
特种医学 | 73篇 |
外科学 | 265篇 |
综合类 | 2篇 |
一般理论 | 1篇 |
预防医学 | 157篇 |
眼科学 | 29篇 |
药学 | 117篇 |
中国医学 | 13篇 |
肿瘤学 | 33篇 |
出版年
2023年 | 15篇 |
2022年 | 35篇 |
2021年 | 65篇 |
2020年 | 42篇 |
2019年 | 50篇 |
2018年 | 73篇 |
2017年 | 48篇 |
2016年 | 48篇 |
2015年 | 62篇 |
2014年 | 95篇 |
2013年 | 119篇 |
2012年 | 148篇 |
2011年 | 192篇 |
2010年 | 100篇 |
2009年 | 69篇 |
2008年 | 100篇 |
2007年 | 111篇 |
2006年 | 73篇 |
2005年 | 80篇 |
2004年 | 66篇 |
2003年 | 40篇 |
2002年 | 62篇 |
2001年 | 32篇 |
2000年 | 33篇 |
1999年 | 27篇 |
1998年 | 16篇 |
1997年 | 14篇 |
1996年 | 17篇 |
1995年 | 16篇 |
1994年 | 11篇 |
1993年 | 12篇 |
1992年 | 21篇 |
1991年 | 11篇 |
1990年 | 10篇 |
1989年 | 19篇 |
1988年 | 9篇 |
1987年 | 8篇 |
1986年 | 7篇 |
1985年 | 15篇 |
1983年 | 6篇 |
1982年 | 6篇 |
1981年 | 7篇 |
1980年 | 8篇 |
1979年 | 4篇 |
1978年 | 11篇 |
1977年 | 5篇 |
1975年 | 7篇 |
1970年 | 6篇 |
1967年 | 5篇 |
1966年 | 3篇 |
排序方式: 共有2057条查询结果,搜索用时 15 毫秒
991.
The present study aimed to investigate the influence of 10 activities on quality of life (QOL) in Japanese older adults and to verify which activities had higher influence on QOL level. The subjects were 465 Japanese community‐dwelling older adults. QOL was assessed by the brief version of the World Health Organization Quality of Life (WHOQOL‐BREF) and the complementary assessment to measure the QOL of older adults (WHOQOL‐OLD) module. Activity and participation were measured through a questionnaire concerning frequency of engagement in several activities. The activity with the highest influence on WHOQOL‐BREF was physical activity (β = 0.209, p < 0.01), followed by art activity (β = 0.169, p < 0.01) and reading and writing (β = 0.141, p < 0.01). The activity with the highest influence on WHOQOL‐OLD was social activity (β = 0.222, p < 0.01), followed by reading and writing activity (β = 0.118, p < 0.05). The limitations of this study were the proportion of subjects and the place of recruitment. Further studies investigating in deep the relation between QOL and activity and participation, and other subjective and environmental factors that may influence the QOL are still needed among a higher and homogeneous subjects sample. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
992.
Brazilian pemphigus foliaceus autoantibodies are pathogenic to BALB/c mice by passive transfer 总被引:13,自引:0,他引:13
J T Roscoe L Diaz S A Sampaio R M Castro R S Labib Y Takahashi H Patel G J Anhalt 《The Journal of investigative dermatology》1985,85(6):538-541
Brazilian pemphigus foliaceus (fogo selvagem) is a cutaneous blistering disease endemic to certain areas of South America that has distinctive epidemiologic features suggestive of an infectious disease transmitted by an insect vector. Patients with the disease have antiepithelial autoantibodies, both circulating in the serum and bound to lesional epidermis. In order to examine the possible pathogenic role of these autoantibodies, IgG from the sera of these patients was purified and injected into the peritoneum of neonatal BALB/c mice. Thirty-four of 46 mice (74%) receiving parenteral IgG fractions from these patients developed cutaneous lesions that were identical to the human disease by clinical, histologic, immunologic, and ultrastructural criteria. High-titer Brazilian pemphigus foliaceus sera produced lesions more consistently and rapidly than low-titer sera. When injections were discontinued, new lesions ceased to appear and old lesions resolved. The extent of disease correlated with the titer of human antiepithelial antibodies detected in the mouse serum (z less than 0.01). Similar concentrations of IgG fractions obtained from sera of unaffected Brazilians living in endemic areas and from American donors did not induce disease when injected into littermates. These results establish that the antiepithelial autoantibodies play an important role in the pathogenesis of the cutaneous lesions in Brazilian pemphigus foliaceus. 相似文献
993.
Marco Antonio de Oliveira-Filho Marcelo Souza Fernando Issamu Tabushi Luís Eduardo Almeida Fernanda Piraj Figueiredo Elora Sampaio Loureno Allan Fernando Giovanini Osvaldo Malafaia Jurandir Marcondes Ribas Filho 《Acta cirúrgica brasileira / Sociedade Brasileira para Desenvolvimento Pesquisa em Cirurgia》2021,36(6)
994.
995.
996.
997.
M. Z. Molnar E. Streja C. P. Kovesdy S. Bunnapradist M. S. Sampaio J. Jing M. Krishnan A. R. Nissenson G. M. Danovitch K. Kalantar‐Zadeh 《American journal of transplantation》2011,11(4):725-736
A body mass index (BMI) below morbid obesity range is often a requirement for kidney transplant wait‐listing, but data linking BMI changes to mortality during the waitlist period are lacking. By linking the 6‐year (7/2001–6/2007) national databases of a large dialysis organization and the Scientific Registry of Transplant Recipients, we identified 14 632 waitlisted hemodialysis patients without kidney transplantation. Time‐dependent survival models examined the mortality predictability of 13‐week‐averaged BMI, pretransplant serum creatinine as a muscle mass surrogate and their changes over time. The patients were on average 52 ± 13 years old, 40% women and had a BMI of 26.9 ± 6.3 kg/m2. Each kg/m2 increase of BMI was associated with a death hazard ratio (HR) of 0.96 (95%CI: 0.95–0.97). Compared to the lowest creatinine quintile, the 4th and 5th quintiles had death HRs of 0.75 (0.66–0.86) and 0.57 (0.49–0.66), respectively. Compared to minimal (< ± 1 kg) weight change over 6 months, those with 3 kg–<5 kg and ≥5 kg weight loss had death HRs of 1.31 (1.14–1.52) and 1.51 (1.30–1.75), respectively. Similar associations were observed with creatinine changes over time. Transplant‐waitlisted hemodialysis patients with lower BMI or muscle mass and/or unintentional weight or muscle loss have higher mortality in this observational study. Impact of intentional weight change remains unclear. 相似文献
998.
999.
Galvão-de Almeida A Quarantini LC Sampaio AS Lyra AC Parise CL Paraná R de Oliveira IR Koenen KC Miranda-Scippa A Guindalini C 《Brain, behavior, and immunity》2011,25(7):1491-1497
Background
Major depression is a frequent adverse effect of interferon-alpha (IFN-α) therapy. Although the indoleamine 2,3-dioxygenase (IDO) enzyme seems to be involved in the pathophysiology of IFN-α-induced depression, no pharmacogenetic study has investigated whether variation in the IDO gene modifies vulnerability to this adverse effect.Methods
A cross-sectional study assessing 277 hepatitis C patients recruited in two specialized outpatient clinics of Brazil. They were interviewed with the Mini International Neuropsychiatric Interview (MINI) approximately 1 month after the end of IFN-α plus ribavirin therapy. Genomic DNA of individuals was extracted from venous blood. Three IDO single-nucleotide polymorphisms (SNPs) were genotyped (rs3824259; rs10089084 and rs35099072).Results
MINI indicated that 21.3% of the sample met criteria for a major depressive episode during the course of IFN-α therapy. No association with the diagnosis of a major depressive episode during the course of IFN-α therapy was observed genotype or allele-wise (p > 0.05). Current major depression and/or current anxiety disorder was significantly associated with IFN-α-related depression (p < 0.005). However, gender, age, route of infection, result of the antiviral treatment, past history of substance use disorders, depression or any other psychiatric disorder showed no association with IFN-α-related depression (p > 0.05).Conclusions
Our results suggest no influence of the variants in the IDO gene and the diagnosis of interferon-α-related depression in the Brazilian population. Interferon-α-related depression may impose persistent psychopathology on at least 15% of the depressed patients even 2 years after antiviral therapy termination. The cross-sectional design is a limitation of our study, predisposing memory bias. Prospective pharmacogenetic studies are warranted to continue investigation of the impact of IDO polymorphisms on the development of IFN-α-induced depression. 相似文献1000.
Rossi NF Sampaio A Gonçalves OF Giacheti CM 《Research in developmental disabilities》2011,32(6):2957-2962
Williams syndrome (WS) is a neurodevelopmental genetic disorder, often referred as being characterized by dissociation between verbal and non-verbal abilities, although the number of studies disputing this proposal is emerging. Indeed, although they have been traditionally reported as displaying increased speech fluency, this topic has not been fully addressed in research. In previous studies carried out with a small group of individuals with WS, we reported speech breakdowns during conversational and autobiographical narratives suggestive of language difficulties. In the current study, we characterized the speech fluency profile using an ecologically based measure--a narrative task (story generation) was collected from a group of individuals with WS (n = 30) and typically developing group (n = 39) matched in mental age. Oral narratives were elicited using a picture stimulus--the cookie theft picture from Boston Diagnosis Aphasia Test. All narratives were analyzed according to typology and frequency of fluency breakdowns (non-stuttered and stuttered disfluencies). Oral narratives in WS group differed from typically developing group, mainly due to a significant increase in the frequency of disfluencies, particularly in terms of hesitations, repetitions and pauses. This is the first evidence of disfluencies in WS using an ecologically based task (oral narrative task), suggesting that these speech disfluencies may represent a significant marker of language problems in WS. 相似文献