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51.
Yoichi Iizuka Haku Iizuka Tokue Mieda Tsuyoshi Tajika Atsushi Yamamoto Kenji Takagishi 《Journal of orthopaedic science》2014,19(5):786-791
Background The concept of “locomotive syndrome” (LS) was proposed by the Japanese Orthopaedic Association (JOA) in 2007 to refer to the risk of elderly individuals becoming bedridden because of reduced function of locomotive organs, for example muscles, bones, and joints. The purpose of this study was to clarify the association between LS screening results based on “loco-check” and health-related quality of life (HRQoL) assessed by use of EuroQol.Materials and methods Four-hundred and forty-two Japanese subjects (183 males and 259 females) were evaluated for LS and HRQoL by use of “loco-check,” EuroQol-5 dimensions (EQ-5D), and EuroQol-VAS (EQ-VAS). If the subjects answered “yes” to one or more of the seven items of “loco-check,” they were assigned to a locomotive syndrome suspected group (L group). If they answered “no” to all seven items, they were assigned to a locomotive syndrome not suspected group (NL group). We investigated the association between the screening LS results obtained by use of “loco-check” and HRQoL status determined by use of EQ-5D utility value and EQ-VAS score.Results LS was suspected among 39.6 % of the subjects on the basis of “loco-check.” In univariate analysis, significantly higher age, higher female-to-male ratio, and more reduced HRQoL were observed in the L group than in the NL group, according to EQ-5D and EQ-VAS. Logistic regression analysis showed that EQ-5D utility value and EQ-VAS score were associated with LS and the difference was statistically significant. Furthermore, correlations were found between the number of items with a “yes” answer on “loco-check”, EQ-5D, or EQ-VAS. That is, a larger number of items with a “yes” answer on “loco-check” was associated with reduced HRQoL assessed by use of EQ-5D and EQ-VAS.Conclusions We demonstrated that a finding of LS on the basis of “loco-check” is significantly associated with EQ-5D utility value and EQ-VAS score, and that a population identified as having LS by use of “loco-check” also had reduced HRQoL. Furthermore, it is speculated that the severity of reduced HRQoL because of locomotive dysfunction can be determined by use of “loco-check”. 相似文献
52.
Cystic cavernous hemangioma of the liver 总被引:2,自引:0,他引:2
Toshihiko Hihara M.D. Tsutomu Araki Kunitaka Katou Hiroaki Odashima Hiroshi Ounishi Kenji Kachi Guio Uchiyama 《Abdominal imaging》1990,15(1):112-114
We report an unusual case of multilocular cystic cavernous hemangioma of the liver. The patient was a 61-year-old woman without liver disfunction but who had multicystic mass lesions in the liver. Although cavernous hemangiomas are usually accurately diagnosed by the various imaging modalities, our case showed atypical features. 相似文献
53.
Masahide Goto Hirofumi Komaki Takashi Saito Yoshiaki Saito Eiji Nakagawa Kenji Sugai Masayuki Sasaki Ichizo Nishino Yu-ichi Goto 《Brain & development》2014
The m.3302A>G mutation in the mitochondrial tRNALeu(UUR) gene has been identified in only 12 patients from 6 families, all manifesting adult-onset slowly progressive myopathy with minor central nervous system involvement. An 11-year-old boy presented with progressive proximal-dominant muscle weakness from age 7 years. At age 10, he developed recurrent stroke-like episodes. Mitochondrial myopathy, encephalopathy, lactic acidosis, plus stroke-like episodes (MELAS) was diagnosed by clinical symptoms and muscle biopsy findings. Mitochondrial gene analysis revealed a heteroplasmic m.3302A>G mutation. Histological examination showed strongly SDH reactive blood vessels (SSVs), not present in previous cases with myopathies due to the m.3302A>G mutation. These findings broaden the phenotypic spectrum of this mutation. 相似文献
54.
Yukari Endo Yoshiaki Saito Taisuke Otsuki Akio Takahashi Yasuhiro Nakata Kazue Okada Mayumi Hirozane Takanobu Kaido Yuu Kaneko Eiko Takada Tetsuya Okazaki Takashi Enokizno Takashi Saito Hirofumi Komaki Eiji Nakagawa Kenji Sugai Masayuki Sasaki 《Brain & development》2014
An 8-year-old boy underwent a resection for focal cortical dysplasia at the left supplementary motor area (SMA) for the treatment of intractable epilepsy. The manifestations of SMA syndrome, such as transient mutism and right hemiparesis, resolved within a few weeks. Verbal disfluency and impaired executive function, accompanied by impulsivity and distractibility, persisted for more than 12 months. The verbal and behavioral problems caused serious difficulties in the school life of the patient, until they became less evident at 18 months after surgery. Tractography performed 18 months after surgery revealed a defect in the subportion of fronto-parietal association fibers within the left superior longitudinal fascicles. Verbal influency can persist with unusually long duration after resection of SMA during childhood. Although not discernible on the routine neuroimaging, white matter damage beneath the SMA region could result in serious disabilities in executive function. These complications should be recognized for the prediction and assessment of deficits in children after surgical intervention involving this region. 相似文献
55.
Stem cell factor‐activated bone marrow ameliorates amyotrophic lateral sclerosis by promoting protective microglial migration 下载免费PDF全文
Tomoya Terashima Hideto Kojima Hiroshi Urabe Isamu Yamakawa Nobuhiro Ogawa Hiromichi Kawai Lawrence Chan Hiroshi Maegawa 《Journal of neuroscience research》2014,92(7):856-869
Amyotrophic lateral sclerosis (ALS) is a progressive disease associated with motor neuron death. Several experimental treatments, including cell therapy using hematopoietic or neuronal stem cells, have been tested in ALS animal models, but therapeutic benefits have been modest. Here we used a new therapeutic strategy, bone marrow transplantation (BMT) with stem cell factor (SCF)‐ or FMS‐like tyrosine kinase 3 (flt3)‐activated bone marrow (BM) cells for the treatment of hSOD1(G93A) transgenic mice. Motor function and survival showed greater improvement in the SCF group than in the group receiving BM cells that had not been activated (BMT alone group), although no improvement was shown in the flt3 group. In addition, larger numbers of BM‐derived cells that expressed the microglia marker Iba1 migrated to the spinal cords of recipient mice compared with the BMT‐alone group. Moreover, after SCF activation, but not flt3 activation or no activation, the migrating microglia expressed glutamate transporter‐1 (GLT‐1). In spinal cords in the SCF group, inflammatory cytokines tumor necrosis factor‐α and interleukin‐1β were suppressed and the neuroprotective molecule insulin‐like growth factor‐1 increased relative to nontreatment hSOD1(G93A) transgenic mice. Therefore, SCF activation changed the character of the migrating donor BM cells, which resulted in neuroprotective effects. These studies have identified SCF‐activated BM cells as a potential new therapeutic agent for the treatment of ALS. © 2014 Wiley Periodicals, Inc. 相似文献
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Miki Ohta Masahito Kobayashi Kenji Wakiya Sachiko Takamizawa Mamoru Niitsu Takamitsu Fujimaki 《Acta neurochirurgica》2014,156(3):565-569