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排序方式: 共有383条查询结果,搜索用时 46 毫秒
51.
Letourneau PA Shackett B Xiao L Trent J Tsao KJ Lally K Hayes-Jordan A 《Journal of pediatric surgery》2011,46(2):332-335
Background
Ewing sarcoma (ES) is the second most common bone tumor in children, and survival of those with metastatic ES has not improved. Previous studies have shown a survival benefit to whole lung irradiation in patients with pulmonary metastases and may be given either before, after, or instead of surgical pulmonary metastasectomy (PM). The contribution of surgery compared with irradiation in ES has not previously been studied.Methods
A retrospective review of patients younger than 21 years (median age, 16 years) treated at a single institution (1990-2006) was performed. Kaplan-Meier survival curves were compared using log-rank test and a multivariate Cox proportional hazards model. P ≤ .05 was regarded as significant.Results
Eighty patients with ES were identified. Of these, 31 (39%) had pulmonary metastases. Nine patients had incomplete details of their full treatment regimen, but the following groups could be defined from the remainder: resection alone (n = 5), radiation alone (n = 3), radiation and resection (n = 3), or chemotherapy alone (n = 11). There were 24 deaths overall, with a median overall survival (OS) of 2.7 (95% confidence interval [CI], 1.7-5.2) years. Patients who had PM had the best OS (80%), whereas those who underwent radiation to the lung without PM compared with chemotherapy only for pulmonary metastasis both had similar OS of 0% at 5 years (P = .002). Patients who had radiation followed by PM for lung metastasis had a 5-year OS of 65%. Patients with PM had a longer OS compared with those without lung resection (P < .0001).Conclusion
These data suggest a possible benefit for ES patients who undergo surgical resection of lung metastases. 相似文献52.
Stewart MJ Greaves L Kushner KE Letourneau NL Spitzer DL Boscoe M 《Health care for women international》2011,32(5):359-383
Efforts to assist low-income women with tobacco reduction and cessation have typically not been informed by assessment of their needs and wishes. This multi-site qualitative study focused on assessing 64 low-income women's support needs and intervention preferences. These women were interested in smoking cessation, but identified many barriers and needed appropriate supports. However, available smoking cessation programs did not address underlying conditions, such as income instability and stress. The support recommended was psychosocial (e.g., buddy and group support), included self-care (e.g., nutrition, activity, and personal time), and reflected their social-economic circumstances (e.g., free cessation aids and child care). 相似文献
53.
Duraisamy Kempuraj Man Huang Kristiana Kandere William Boucher Richard Letourneau Sheila Jeudy Kim Fitzgerald Kathleen Spear Achilles Athanasiou Theoharis C Theoharides 《Annals of allergy, asthma & immunology》2002,88(5):501-506
BACKGROUND: Mast cells are involved in early- and late-phase reactions by releasing vasoactive molecules, proteases, and cytokines. Certain histamine-1 receptor antagonists and other antiallergic drugs seem to inhibit the release of mediators from rat and human mast cells. OBJECTIVE: Azelastine and olopatadine are antiallergic agents present in the ophthalmic solutions azelastine hydrochloride (Optivar, Asta Medica/Muro Pharmaceuticals, Tewksbury, MA), and olopatadine hydrochloride (Patanol, Alcon Laboratories, Fort Worth, TX), respectively. We investigated the effect of these drugs on interleukin-6 (IL-6), tryptase, and histamine release from cultured human mast cells (CHMCs). METHODS: CHMCs were grown from human umbilical cord blood-derived CD34+ cells in the presence of stem cell factor and IL-6 for 14 to 16 weeks. Sensitized CHMCs were pretreated with various concentrations of azelastine or olopatadine for 5 minutes. CHMCs were then challenged with anti-immunoglobulin E, and the released mediators were quantitated. RESULTS: The greatest inhibition of mediator release was seen with 24 microM azelastine; this level of inhibition was matched with the use of 133 microM olopatadine. At this concentration, these drugs inhibited IL-6 release by 83% and 74%, tryptase release by 55% and 79%, and histamine release by 41% and 45%, respectively. Activated CHMCs were characterized by numerous filopodia that were inhibited by both drugs as shown by electron microscopy. CONCLUSIONS: These results indicate that azelastine and olopatadine can inhibit CHMCs activation and release of IL-6, tryptase, and histamine. On an equimolar basis, azelastine was a more potent inhibitor than olopatadine. 相似文献
54.
55.
M Alexandrakis L Singh W Boucher R Letourneau P Theofilopoulos T C Theoharides 《International journal of immunopharmacology》1999,21(6):379-390
Rat basophilic leukemia (RBL) cells resemble mucosal mast cells (MMC) and develop few secretory granules under normal culture conditions. RBL cells have been used for the study of secretion and for the possible involvement of MMC in food allergies and irritable bowel syndrome (IBS). The flavonoid quercetin is one of very few molecules that inhibit RBL cell proliferation and constitutive histamine release; it also induces synthesis of rat mast cell protease (RMCP) II and accumulation of secretory granules. Even though quercetin is available as a food supplement over the counter, some early studies had indicated it may be carcinogenic. We, therefore, compared the effect of quercetin to that of other flavonoids with similar structure. Flavone, kaempferol, myricetin and morin were investigated for their action on RBL cell secretion of beta-hexosaminidase stimulated by anti-DNP serum and DNP-BSA, as well as on secretory granule development. Quercetin, myricetin and kaempferol inhibited RBL cell secretion significantly only at 10(-4) M. Flavone inhibited secretion at 10(-4), 10(-5) and 10(-6) M; it also maximally induced secretory granule accumulation as evidenced by light and electron microscopy. In contrast, morin which differs structurally only by one extra hydroxyl group had minimal effect. These results indicate that flavone is capable of inhibiting stimulated secretion and inducing secretory granule development at reasonable concentrations. 相似文献
56.
Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer. 总被引:32,自引:0,他引:32
S Giacchetti B Perpoint R Zidani N Le Bail R Faggiuolo C Focan P Chollet J F Llory Y Letourneau B Coudert F Bertheaut-Cvitkovic D Larregain-Fournier A Le Rol S Walter R Adam J L Misset F Lévi 《Journal of clinical oncology》2000,18(1):136-147
PURPOSE: To study how adding oxaliplatin (l-OHP) to chronomodulated fluorouracil (5-FU)-leucovorin (LV) affected the objective response rate, as first-line treatment of metastatic colorectal cancer. PATIENTS AND METHODS: Two hundred patients from 15 institutions in four countries were randomly assigned to receive a 5-day course of chronomodulated 5-FU and LV (700 and 300 mg/m(2)/d, respectively; peak delivery rate at 0400 hours) with or without l-OHP on the first day of each course (125 mg/m(2), as a 6-hour infusion). Each course was repeated every 21 days. Response was assessed by extramural review of computed tomography scans. RESULTS: Grade 3 to 4 toxicity from 5-FU-LV occurred in = 5% of the patients (= 1% of the courses). Grade 3 to 4 diarrhea occurred in 43% of the patients given l-OHP (10% of the courses), and less than 2% of the patients had severe hematotoxicity. Thirteen percent of the patients had moderate functional impairment from peripheral sensory neuropathy. Sixteen percent of the patients receiving 5-FU-LV had an objective response (95% confidence interval [CI], 9% to 24%), compared with 53% of those receiving additional l-OHP (95% CI, 42% to 63%) (P <. 001). The median progression-free survival time was 6.1 months with 5-FU-LV (range, 4.1 to 7.4 months) and 8.7 months (7.4 to 9.2 months) with l-OHP and 5-FU-LV (P =.048). Median survival times were 19.9 and 19.4 months, respectively. CONCLUSION: By chronomodulating 5-FU-LV, we were able to add l-OHP without compromising dose-intensities. l-OHP significantly improved the antitumor efficacy of this regimen. 相似文献
57.
58.
Doucet S Jones I Letourneau N Dennis CL Blackmore ER 《Archives of women's mental health》2011,14(2):89-98
Postpartum psychosis is a serious disorder that can cause negative consequences for the mother, infant, and entire family.
While reports of this condition date back for centuries, little is known about what interventions are most effective for this
population. The purpose of this systematic review was to examine the research evidence on interventions for the prevention
and treatment of postpartum psychosis. Studies were searched using CINAHL, EMBASE, MEDLINE, PsycINFO, and PubMed databases.
All primary research studies published in English since 1970 that explored interventions for the prevention or treatment of
postpartum psychosis were included. The search resulted in 26 studies on interventions for postpartum psychosis, with 10 focusing
on prevention and 17 focusing on treatment. Studies on the prevention of postpartum psychosis have examined the effects of
mood stabilizers, antipsychotics, and hormone therapy, while those examining treatment have included electroconvulsive therapy,
mood stabilizers, antipsychotics, hormones, and the beta blocker propranolol. Only preliminary evidence suggests which interventions
may be effective strategies to prevent (e.g., lithium) and treat (e.g., electroconvulsive therapy) postpartum psychosis. Due
to methodological limitations in the studies reviewed, extensive evidence-based recommendations for the prevention and treatment
of postpartum psychosis cannot be made. The known risk factors and negative consequences of postpartum psychosis point to
the importance of preventative and acute treatment measures. Well-designed prospective studies are needed to determine the
efficacy of prevention and treatment interventions for women who experience postpartum psychosis. 相似文献
59.
Niemasik EE Letourneau J Dohan D Katz A Melisko M Rugo H Rosen M 《Journal of cancer survivorship》2012,6(3):324-332
Purpose
We sought to determine what women recall about reproductive health risks (RHR) from cancer therapy at the time of cancer diagnosis in order to identify barriers to reproductive health counseling (RHC) and fertility preservation (FP). 相似文献60.
N. Sinha J. M. Letourneau K. Wald P. Xiong Tal Imbar B. Li E. Harris E. Mok-Lin M. I. Cedars Mitchell P. Rosen 《Journal of assisted reproduction and genetics》2018,35(10):1861-1868