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81.
Taleef R. Khan Kalin R. Pearce Steven J. McAnany Colleen M. Peters Munish C. Gupta Lukas P. Zebala 《The spine journal》2018,18(3):439-446
Background Context
Recombinant human bone morphogenetic protein 2 (rhBMP-2) plays a pivotal role in complex spine surgery. Despite its limited approval, the off-label use of rhBMP-2 is prevalent, particularly in transforaminal lumbar interbody fusions (TLIFs).Purpose
To determine the effectiveness and safety of rhBMP-2 use in TLIF procedures versus autograft.Study Design
Retrospective cohort study.Patient Sample
Patients older than 18 years undergoing spine surgery for lumbar degenerative spine disease at a single academic institution.Outcome Measures
Clinical outcome was determined according to patient records. Radiographic outcome was determined according to plain X-rays and computed tomography (CT).Methods
A retrospective study from 1997 to 2014 was conducted on 191 adults undergoing anterior-posterior instrumented spinal fusion with TLIF at a single academic institution. Patient data were gathered from operative notes, follow-up clinic notes, and imaging studies to determine complications and fusion rates. One hundred eighty-seven patients fit the criteria, which included patients with a minimum of one TLIF, and had a minimum 2-year radiographic and clinical follow-up. Patients were further classified into a BMP group (n=83) or non-BMP group (n=104). Three logistic regression models were run using rhBMP-2 exposure as the independent variable. The respective outcome variables were TLIF-related complications (radiculitis, seroma, osteolysis, and ectopic bone), surgical complications, and all complications.Results
Bone morphogenetic protein (n=83) and non-BMP (n=104) groups had similar baseline demographics (sex, diabetes, pre-existing cancer). On average, the BMP and non-BMP groups were similarly aged (51.9 vs. 47.9 years, p>.05), but the BMP group had a shorter follow-up time (3.03 vs. 4.06 years; p<.001) and fewer smokers (8 vs. 21 patients; p<.048). The fusion rate for the BMP and non-BMP groups was 92.7% and 92.3%, respectively. The pseudoarthrosis rate was 7.5% (14 of 187 patients). Radiculitis was observed in seven patients in the BMP group (8.4%) and two patients in the non-BMP group (1.9%). Seroma was observed in two patients in the BMP group (2.4%) and none in the non-BMP group. No deep infections were observed in the BMP group, and in one patient in the non-BMP group (0.96%). Although patients exposed to BMP were at a significantlygreater risk of developing radiculitis and seroma (odds ratio [OR]=4.53, confidence interval [CI]=1.42–14.5), BMP exposure was not a significant predictor of surgical complications (OR=0.32, CI=0.10–1.00) or overall complications (OR=1.11, CI=0.53–2.34). The outcome of TLIF-related complications was too rare and the confidence interval too wide for practical significance of the first model.Conclusion
Evidence supports the hypothesis that off-label use of rhBMP-2 in TLIF procedures is relatively effective for achieving bone fusion at rates similar to patients receiving autograft. Patients exhibited similar complication rates between the two groups, with the BMP group exhibiting slightly higher rates of radiculitis and seroma. 相似文献82.
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Amy T. Peters Katie L. Burkhouse Autumn Kujawa Kaveh Afshar Kate D. Fitzgerald Christopher S. Monk Greg Hajcak K. Luan Phan 《Developmental psychobiology》2019,61(1):69-80
Anxiety disorders are associated with enhanced error-related negativity (ERN) across development but it remains unclear whether alterations in brain electrophysiology are linked to the timing of puberty. Pubertal timing and alterations of prefrontal and limbic development are implicated in risk for depression, but the interplay of these factors on the ERN–anxiety association has not been assessed. We examined the unique and interactive effects of pubertal timing and depression on the ERN in a sample of youth 10–19 years old with anxiety disorders (n = 30) or no history of psychopathology (n = 30). Earlier pubertal maturation was associated with an enhanced ERN. Among early, but not late maturing youth, higher depressive symptoms were associated with a reduced ERN. The magnitude of neural reactivity to errors is sensitive to anxiety, depression, and development. Early physical maturation and anxiety may heighten neural sensitivity to errors yet predict opposing effects in the context of depression. 相似文献
87.
Corinne Antignac James P. Calvet Gregory G. Germino Jared J. Grantham Lisa M. Guay-Woodford Peter C. Harris Friedhelm Hildebrandt Dorien J.M. Peters Stefan Somlo Vicente E. Torres Gerd Walz Jing Zhou Alan S.L. Yu 《Journal of the American Society of Nephrology : JASN》2015,26(9):2081-2095
Polycystic kidney disease (PKD) is one of the most common life-threatening genetic diseases. Jared J. Grantham, M.D., has done more than any other individual to promote PKD research around the world. However, despite decades of investigation there is still no approved therapy for PKD in the United States. In May 2014, the University of Kansas Medical Center hosted a symposium in Kansas City honoring the occasion of Dr. Grantham''s retirement and invited all the awardees of the Lillian Jean Kaplan International Prize for Advancement in the Understanding of Polycystic Kidney Disease to participate in a forward-thinking and interactive forum focused on future directions and innovations in PKD research. This article summarizes the contributions of the 12 Kaplan awardees and their vision for the future of PKD research. 相似文献
88.
Vascular Management During Live Donor Nephrectomy: An Online Survey Among Transplant Surgeons 下载免费PDF全文
S. Janki D. Verver K. W. J. Klop A. L. Friedman T. G. Peters L. E. Ratner J. N. M. Ijzermans F. J. M. F. Dor 《American journal of transplantation》2015,15(6):1701-1707
89.
Markus G. Seidel Katrin Böhm Figen Dogu Austen Worth Adrian Thrasher Benoit Florkin Aydan İkincioğulları Anke Peters Shahrzad Bakhtiar Marie Meeths Polina Stepensky Isabelle Meyts Svetlana O. Sharapova Laura Gámez-Díaz Lennart Hammarström Stephan Ehl Bodo Grimbacher Andrew R. Gennery 《The Journal of allergy and clinical immunology》2018,141(2):770-775.e1
90.
Mari Sasaki Jennifer J. Koplin Shyamali C. Dharmage Michael J. Field Susan M. Sawyer Vicki McWilliam Rachel L. Peters Lyle C. Gurrin Peter J. Vuillermin Jo Douglass Angela Pezic Maia Brewerton Mimi L.K. Tang George C. Patton Katrina J. Allen 《The Journal of allergy and clinical immunology》2018,141(1):391-398.e4