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排序方式: 共有1203条查询结果,搜索用时 15 毫秒
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Kirsi Murtomäki MD Tuomas Mertsalmi MD Elina Jaakkola MD PhD Elina Mäkinen MD PhD Reeta Levo RN Tanja Nojonen RN Mikael Eklund BM Simo Nuuttila BM Kari Lindholm RN Eero Pekkonen MD PhD Juho Joutsa MD PhD Tommi Noponen PhD Toni Ihalainen PhD Valtteri Kaasinen MD PhD Filip Scheperjans MD PhD 《Movement disorders》2022,37(6):1284-1289
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Diana Bell Ehab Y. Hanna Randal S. Weber Franco DeMonte Asterios Triantafyllou James S. Lewis Antonio Cardesa Pieter J. Slootweg Gran Stenman Douglas R. Gnepp Kenneth O. Devaney Juan P. Rodrigo Alessandra Rinaldo Bruce M. Wenig William H. Westra Justin A. Bishop Henrik Hellquist Jennifer L. Hunt Kimihide Kusafuka Bayardo PerezOrdoez Michelle D. Williams Robert P. Takes Alfio Ferlito 《Head & neck》2016,38(Z1):E2259-E2266
Neuroendocrine neoplasms of the sinonasal region, which are relatively uncommon but clinically very important, are reviewed here in the light of current knowledge. Using a definition for neuroendocrine based on phenotypic, histologic, immunohistochemical, and electron microscopic features rather than histogenetic criteria, sinonasal neuroendocrine carcinomas are examined with a particular emphasis on the small‐cell and large‐cell subtypes. This is followed by revisiting olfactory neuroblastoma because it is also a tumor that shows a neuroendocrine phenotype. Kadish clinical and Hyams histologic grading systems as prognosticators of olfactory neuroblastoma are also considered in detail. Finally, controversies regarding sinonasal undifferentiated carcinoma as a neuroendocrine tumor are discussed and a possible relationship with high‐grade olfactory neuroblastoma is explored. Genetic events and current management of these tumors are also outlined. © 2015 Wiley Periodicals, Inc. Head Neck 38 : E2259–E2266, 2016 相似文献
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Meredith Achey BM Jason L. Aldred MD Noha Aljehani MD Bastiaan R. Bloem MD PhD Kevin M. Biglan MD MPH Piu Chan MD PhD Esther Cubo MD PhD E. Ray Dorsey MD MBA Christopher G. Goetz MD Mark Guttman MD Anhar Hassan MB BCh FRACP Suketu M. Khandhar MD Zoltan Mari MD Meredith Spindler MD Caroline M. Tanner MD PhD Pieter van den Haak MSc Richard Walker MD Jayne R. Wilkinson MD 《Movement disorders》2014,29(7):871-883
Travel distance, growing disability, and uneven distribution of doctors limit access to care for most Parkinson's disease (PD) patients worldwide. Telemedicine, the use of telecommunications technology to deliver care at a distance, can help overcome these barriers. In this report, we describe the past, present, and likely future applications of telemedicine to PD. Historically, telemedicine has relied on expensive equipment to connect single patients to a specialist in pilot programs in wealthy nations. As the cost of video conferencing has plummeted, these efforts have expanded in scale and scope, now reaching larger parts of the world and extending the focus from care to training of remote providers. Policy, especially limited reimbursement, currently hinders the growth and adoption of these new care models. As these policies change and technology advances and spreads, the following will likely develop: integrated care networks that connect patients to a wide range of providers; education programs that support patients and health care providers; and new research applications that include remote monitoring and remote visits. Together, these developments will enable more individuals with PD to connect to care, increase access to expertise for patients and providers, and allow more‐extensive, less‐expensive participation in research. © 2014 International Parkinson and Movement Disorder Society 相似文献
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Andrea K. Vaags PhD Sarah Bowdin BM MSc MRCPCH Mary‐Lou Smith PhD Brigitte Gilbert‐Dussardier MD Katja S. Brocke‐Holmefjord MD Katia Sinopoli PhD CPsych Cindy Gilles MSc Tove B. Haaland MD Catherine Vincent‐Delorme MD Emmanuelle Lagrue MD Radu Harbuz MD Susan Walker PhD Christian R. Marshall PhD Gunnar Houge MD PhD Vera M. Kalscheuer PhD Stephen W. Scherer PhD Berge A. Minassian MD 《Annals of neurology》2014,76(5):758-764
Synaptic function is central to brain function. Understanding the synapse is aided by studies of patients lacking individual synaptic proteins. Common neurological diseases are genetically complex. Their understanding is likewise simplified by studies of less common monogenic forms. We detail the disease caused by absence of the synaptic protein CNKSR2 in 8 patients ranging from 6 to 62 years old. The disease is characterized by intellectual disability, attention problems, and abrupt lifelong language loss following a brief early childhood epilepsy with continuous spike‐waves in sleep. This study describes the phenotype of CNKSR2 deficiency and its involvement in systems underlying common neurological disorders. Ann Neurol 2014;76:758–764 相似文献
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Brian C. Case MD Sant Kumar BA Charan Yerasi MD Brian J. Forrestal MBBS Anees Musallam MD Chava Chezar-Azerrad MD Nauman Khalid MD Evan Shlofmitz DO Yuefeng Chen MD PhD Jaffar M. Khan BM BCh PhD Lowell F. Satler MD Itsik Ben-Dor MD Hayder Hashim MD Nelson L. Bernardo MD Toby Rogers MD PhD Ron Waksman MD 《Catheterization and cardiovascular interventions》2021,98(3):572-577
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Jaffar M. Khan BM BCh Robert J. Lederman MD 《Catheterization and cardiovascular interventions》2018,91(6):1052-1053
- Transcatheter electrosurgery has emerging value in a range of other new procedures that require traversing tissue (transcaval access, transcatheter Glenn Shunt) or slicing tissue (LAMPOON slicing of the mitral valve and BASILICA slicing of the aortic valve).
- This is the first report of bipolar radiofrequency wires used to cross lesions in humans, reported here in seven re‐entry CTO cases.
- The bipolar configuration may provide directionality to charge without need for wire alignment and advancement, but is theoretically disadvantageous for tissue “cutting” because of problems with charge concentration.