全文获取类型
收费全文 | 264篇 |
免费 | 3篇 |
专业分类
耳鼻咽喉 | 1篇 |
儿科学 | 63篇 |
妇产科学 | 2篇 |
基础医学 | 44篇 |
口腔科学 | 3篇 |
临床医学 | 28篇 |
内科学 | 65篇 |
皮肤病学 | 17篇 |
神经病学 | 2篇 |
外科学 | 18篇 |
预防医学 | 12篇 |
药学 | 12篇 |
出版年
2017年 | 2篇 |
2015年 | 2篇 |
2014年 | 3篇 |
2010年 | 4篇 |
2009年 | 5篇 |
2008年 | 4篇 |
2007年 | 5篇 |
2001年 | 2篇 |
1999年 | 2篇 |
1998年 | 3篇 |
1997年 | 11篇 |
1996年 | 11篇 |
1995年 | 7篇 |
1994年 | 12篇 |
1993年 | 9篇 |
1992年 | 6篇 |
1991年 | 3篇 |
1990年 | 8篇 |
1989年 | 15篇 |
1988年 | 9篇 |
1987年 | 15篇 |
1986年 | 15篇 |
1985年 | 10篇 |
1984年 | 11篇 |
1983年 | 8篇 |
1982年 | 8篇 |
1981年 | 6篇 |
1980年 | 10篇 |
1979年 | 7篇 |
1978年 | 4篇 |
1977年 | 3篇 |
1976年 | 5篇 |
1974年 | 3篇 |
1972年 | 3篇 |
1971年 | 8篇 |
1970年 | 1篇 |
1968年 | 1篇 |
1967年 | 2篇 |
1966年 | 2篇 |
1964年 | 1篇 |
1963年 | 1篇 |
1960年 | 1篇 |
1958年 | 2篇 |
1957年 | 2篇 |
1956年 | 2篇 |
1940年 | 1篇 |
1939年 | 1篇 |
1932年 | 1篇 |
1928年 | 1篇 |
1925年 | 1篇 |
排序方式: 共有267条查询结果,搜索用时 15 毫秒
121.
Risk factors for heart failure in the general population: The study of men born in 1913 总被引:3,自引:2,他引:3
ERIKSSON H.; SVaRDSUDD K.; LARSSON B.; OHLSON L. O.; TIBBLIN G.; WELIN L.; WILHELMSEN L. 《European heart journal》1989,10(7):647-656
In 1963 a sample of 973 men, all 50 years old, was drawn fromthe population register of Gothenburg, Sweden. These men havebeen followed up for 17 years with repeated examinations regardinga number of variables possibly related to cardiovascular disease.The latest examination, at the age of 67 years, focused on congestiveheart failure (CHF). The incidence rate of manifest CHF variedfrom 1·5 to 10·2 cases (1000 population)1yr1, depending on which age group was being studied.For the age group 5067 years the incidence of manifestCHF was 5·5 (1000)1 yr1. A large numberof factors associated with the risk of acquiring CHF were identified.In multivariate regression analyses, hypertension and smokingwere the major independent risk factors. Body weight, heartvolume, T-wave abnormalities, heart rate variability, peak expiratoryflow rate, psychological stress and Fy-antigen (a genetic marker?)were also independent risk factors. Possible strategies forprevention are discussed. 相似文献
122.
Metabolic disturbances in hypertension: results from the population study 'men born in 1913'. 总被引:2,自引:0,他引:2
H. ERIKSSON L. WELIN L. WILHELMSEN B. LARSSON L.-O. OHLSON K. SVRDSUDD G. TIBBLIN 《Journal of internal medicine》1992,232(5):389-395
A clustering of metabolic disturbances has been indicated in hypertension. The distribution of such factors was assessed among hypertensives and normotensives in a general population sample of 644 men aged 67 years. Fasting serum insulin, glucose and triglyceride levels were measured. In this study hypertension was defined as DBP > or = 95 mmHg or present use of antihypertensives. Impaired glucose tolerance (IGT) or diabetes mellitus, hyperinsulinaemia (> or = 20 mU l-1) and hypertriglyceridaemia (> or = 2.3 mmol l-1) were defined as metabolic disturbances. When all these disturbances were present simultaneously a complete 'metabolic syndrome' was considered to be present. Hypertension was found in 185 (29%) men, IGT in 15%, diabetes mellitus in 11%, hyperinsulinaemia in 18% and hypertriglyceridaemia in 19%. Among hypertensives, 11 (6%) men had a 'metabolic syndrome', compared to 12 (3%) men in the normotensive group (P = 0.039). At least one metabolic disturbance was present in 109 (59%) of the hypertensive men, and in 173 (38%) of the normotensive men (P < 0.001). The prevalence rates of metabolic disturbances did not differ significantly between lean (BMI < 26 kg m-2) and obese (BMI > or = 26 kg m-2) hypertensives. Only hypertriglyceridaemia was more frequent in obese than in lean hypertensives (20% vs. 37%, P = 0.015). The 'metabolic syndrome' was found in 6% of all hypertensives, which was twice as common as in the normotensive population. The 'metabolic syndrome' was uncommon in both lean and obese hypertensives (5% vs. 7%, NS). These findings indicate that hypertension and metabolic disturbances may have a common underlying cause, at least in some individuals. 相似文献
123.
QING YI INGRID ERIKSSON WEN HE GO¨RAN HOLM HÅKAN MELLSTEDT & ANDERS O¨STERBORG 《British journal of haematology》1997,96(2):338-345
Tumour-specific CD4+ T helper (Th) and CD8+ T cytotoxic (Tc) cells may participate in the control and eradication of tumour cells. In the present study, idiotype-specific stimulation of CD4+ and CD8+ blood T cells from patients with monoclonal gammopathy of undetermined significance and patients with untreated multiple myeloma stage I was examined. Activation was measured in the CD4+ and CD8+ subsets enriched by magnetic microbeads as the incorporation of 3H-thymidine and the secretion of interferon (IFN)-γ, interleukin (IL)-2 and IL-4 by single cells using the enzyme-linked immunospot assay. Idiotype-specific T cells were found in four of seven patients. Stimulation was mainly confined to the CD4+ subset in three of the four responding patients. This type of response was major histocompatibility complex (MHC) class II restricted as it could be inhibited by monoclonal antibodies against MHC class II (HLA-DR), but not against class I (HLA-ABC) molecules. Idiotype-specific CD8+ T cells were also demonstrated in these patients although at a lower frequency. One patient showed a strong and dominating activation of CD8+ T cells which could be blocked by antibodies against HLA-ABC but not against HLA-DR. Idiotype-specific CD4+ or CD8+ T cells were mainly of the type-1 subsets as judged by their secretion of IFN-γ and IL-2. Thus, this study provides evidence for the presence of idiotype-specific and MHC-restricted CD4+ and CD8+ T cells of the type-1 subsets in patients with monoclonal gammopathies. Such T cells with the potential to control the growth of tumour B cells may be a suitable target for immunotherapeutic interventions in patients. 相似文献
124.
125.
126.
127.
BRUUSGAARD DAG; NESSI{varphi}Y INGE; RUTLE OLAV; FURUSETH KRISTIAN; NATVIG BARD 《Family practice》1993,10(2):212-218
In a population study, a random sample of 398 persons from 20to 72 years answered the six item version of the Dartmouth COOPfunctional health assessment charts/WONCA. The results accordingto age and sex are presented. The charts have been developedprimarily for use in clinical settings. In a cross-sectionalstudy in a normal population, the instrument seems feasiblein use and it differentiates between the sexes and age groups. 相似文献
128.
O. WIKLUND B. ANGELIN G. FAGER M. ERIKSSON S.-O. OLOFSSON L. BERGLUND T. LINDEN A. SJ
BERG G. BONDJERS 《Journal of internal medicine》1990,228(3):241-247
Abstract. The efficacy and safety of a new, selective inhibitor of cholesterol synthesis, pravastatin, and the bile acid-binding resin, cholestyramine, were compared in a randomized, double-blind study of 120 patients with familial hypercholesterolaemia. After a run-in period of 8-10 weeks with assessment of dietary habits, the patients were treated with pravastatin + placebo, placebo + cholestyramine, or placebo alone. Active pravastatin therapy was initiated with 10 mg b.i.d. for 6 weeks, and was increased to 20 mg b.i.d. for the following 6 weeks. Cholestyramine was given at 24 gd?1, or the highest tolerable dose. After 6 weeks of therapy, serum total and LDL cholesterol levels were reduced by 17% and 21%, respectively, on pravastatin treatment, whereas the corresponding reductions with cholestyramine treatment were 24% and 30%, respectively. With an increased dose of pravastatin, serum and LDL cholesterol concentrations were reduced by 23% and 28%, respectively, after 12 weeks; the effect of cholestyramine was unchanged. HDL cholesterol levels increased in response to pravastatin, by 7% and 9% after 6 and 12 weeks, respectively. Concomitant changes in the concentrations of apolipoproteins B and AI were observed. Three patients discontinued the study because of side-effects: two subjects were treated with pravastatin and one was given placebo. The prevalence of side-effects (including laboratory abnormalities) was 35% for pravastatin, 30% for placebo, and 53% (significantly higher) for cholestyramine. We conclude that pravastatin, in a 40 mg daily dose, is as effective as cholestyramine in lowering LDL cholesterol in familial hypercholesterolaemia. Since the frequency of side-effects is higher with cholestyramine, pravastatin offers a promising alternative for the therapy of this genetic disease. 相似文献
129.
B. ERIKSSON H. ARNBERG P.-G. LINDGREN L.-E. L
RELIUS A. MAGNUSSON G. LUNDQVIST B. SKOGSEID L. WIDE E. WILANDER K.
BERG 《Journal of internal medicine》1990,228(2):103-113
Abstract. A prospective study has been performed on 84 patients with endocrine pancreatic tumours evaluated at the Medical Department in Uppsala. Available information concerning the patients' presenting symptoms, age at diagnosis, clinical syndrome, tumour location, location of metastases, diagnostic radiology, biochemical and histopathological findings has been analysed. Our results indicate that most patients initially show rather vague and non-specific symptoms, with dyspepsia and pain being the most frequent presenting features. The median delay between appearance of the first symptom and diagnosis was 2 years; the delay was 3 5 months in sporadic cases and 14.5 months in familial cases. In spite of improvements in diagnostic methods, the median age at diagnosis (53 years) has not been reduced, and most patients are encountered when the tumour has reached an advanced stage. There is a need for a method of screening patients with still uncharacteristic abdominalsymptoms for a neuroendocrine tumour. The presence of elevated levels of plasma chromogranin in all patients with a proven tumour suggests that such possibilities exist, and the use of this biochemical marker in the future might reduce the age at diagnosis and thus improve the likelihood of cure and survival of patients with endocrine pancreatic tumours. 相似文献
130.
Increase of asthma, allergic rhinitis and eczema in Swedish schoolchildren between 1979 and 1991 总被引:18,自引:2,他引:16
Background: A previous study has shown a twofold increase in prevalence of asthma and allergic rhinitis (AR) in Swedish recruits during the 1970s. The increase was higher in more northerly colder regions. Objectives To follow up the previously found trend to increasing prevalences with time as well as the climatic variations within the country. Methods: The prevalences of asthma, allergic rhinitis and eczema were assessed using two questionnaire studies, 12 years apart (1979 and 1991) with identical questions about the diseases. The study comprised representative samples of children from the Göteborg area on the south-western coast (in 1979: 7-year-olds, n= 4255, in 1991: 7-year-olds, n= 1649) and in Kiruna, a mining town in the northernmost inland mountains (in 1979: 7-year-olds, n= 427, in 1991: 7-9-year-olds, n= 832). In 1991 there was also a personal interview and a skin-prick test (SPT) on subsamples. Results: The prevalence of all these diseases present over the last year had roughly doubled over the 12-year period. On both occasions, most symptoms were more prevalent in the northern area. In 1991, the prevalence of one or more symptoms in Goteborg was 23.8% and 32.5% and in Kiruna 29.9% and 44.8% in the questionnaire and the interview, respectively. Conclusion: Asthma, AR and eczema increase continuously in prevalence in Sweden and the climatic distribution of the prevalences suggests possible major risk factors to be found in a closed indoor climate. 相似文献