全文获取类型
收费全文 | 2019篇 |
免费 | 97篇 |
国内免费 | 13篇 |
专业分类
耳鼻咽喉 | 10篇 |
儿科学 | 28篇 |
妇产科学 | 6篇 |
基础医学 | 224篇 |
口腔科学 | 44篇 |
临床医学 | 107篇 |
内科学 | 559篇 |
皮肤病学 | 94篇 |
神经病学 | 111篇 |
特种医学 | 66篇 |
外科学 | 368篇 |
综合类 | 9篇 |
预防医学 | 45篇 |
眼科学 | 10篇 |
药学 | 132篇 |
中国医学 | 6篇 |
肿瘤学 | 310篇 |
出版年
2023年 | 8篇 |
2022年 | 19篇 |
2021年 | 22篇 |
2020年 | 18篇 |
2019年 | 31篇 |
2018年 | 30篇 |
2017年 | 32篇 |
2016年 | 29篇 |
2015年 | 44篇 |
2014年 | 56篇 |
2013年 | 66篇 |
2012年 | 95篇 |
2011年 | 142篇 |
2010年 | 76篇 |
2009年 | 62篇 |
2008年 | 100篇 |
2007年 | 99篇 |
2006年 | 145篇 |
2005年 | 134篇 |
2004年 | 136篇 |
2003年 | 133篇 |
2002年 | 131篇 |
2001年 | 31篇 |
2000年 | 40篇 |
1999年 | 31篇 |
1998年 | 38篇 |
1997年 | 28篇 |
1996年 | 31篇 |
1995年 | 39篇 |
1994年 | 19篇 |
1993年 | 32篇 |
1992年 | 23篇 |
1991年 | 18篇 |
1990年 | 18篇 |
1989年 | 11篇 |
1988年 | 14篇 |
1987年 | 17篇 |
1986年 | 21篇 |
1985年 | 5篇 |
1984年 | 9篇 |
1983年 | 9篇 |
1982年 | 14篇 |
1981年 | 13篇 |
1980年 | 5篇 |
1979年 | 6篇 |
1976年 | 4篇 |
1975年 | 6篇 |
1974年 | 7篇 |
1973年 | 4篇 |
1970年 | 5篇 |
排序方式: 共有2129条查询结果,搜索用时 15 毫秒
81.
Yabe I Kitagawa M Suzuki Y Fujiwara K Wada T Tsubuku T Takeichi N Sakushima K Soma H Tsuji S Niino M Saitoh S Sasaki H 《Journal of neurology》2008,255(10):1541-1544
Clinical examinations and mutational analyses were carried out in three patients of a Japanese familial hemiplegic migraine
(FHM) pedigree. Each affected member demonstrated a broad clinical spectrum that included hemiplegic migraine with progressive
cerebellar ataxia, migraine without aura, and episodic ataxia. Despite this variability, all members exhibited marked downbeat
positioning nystagmus, and magnetic resonance images (MRI) all showed cerebellar atrophy predominantly of the cerebellar vermis.
All affected members had a T666M missense mutation in the protein encoded by the CACNA1A gene (calcium channel, voltage-dependent, P/Q type, alpha 1A subunit). Although clinical features associated with the T666M
CACNA1A mutation are highly variable, downbeat positioning nystagmus may be an important clinical feature of this disease. 相似文献
82.
83.
Ishii K Tamaoka A Otsuka F Iwasaki N Shin K Matsui A Endo G Kumagai Y Ishii T Shoji S Ogata T Ishizaki M Doi M Shimojo N 《Annals of neurology》2004,56(5):741-745
We noted a new clinical syndrome with prominent cerebellar symptoms in apartment building residents in Kamisu, Japan. The well that provided drinking water contained diphenylarsinic acid, a degradation product of diphenylcyanoarsine or diphenylchloroarsine, which were developed for use as chemical weapons, inducing severe vomiting and sneezing. Characteristics of diphenylarsinic acid poisoning include brainstem-cerebellar and cerebral symptoms. Mental retardation associated with brain atrophy in magnetic resonance images was evident in some infants. We must be vigilant to prevent or minimize the effects of further diphenylarsinic acid poisoning in Japan or elsewhere. 相似文献
84.
A case of an epithelioid glioblastoma with the BRAF V600E mutation colocalized with BRAF intact low‐grade diffuse astrocytoma 下载免费PDF全文
Jun‐Ichiro Kuroda Sumihito Nobusawa Hideo Nakamura Hideaki Yokoo Ryuta Ueda Keishi Makino Shigetoshi Yano Jun‐ichi Kuratsu 《Neuropathology》2016,36(2):181-186
Epithelioid glioblastomas are one of the rarest histological variants of glioblastomas, which are not formally recognized by the World Health Organization (WHO) classification. Epithelioid glioblastomas usually occur as primary lesions, but there have been several reports of secondary epithelioid glioblastomas or epithelioid glioblastomas with pre‐ or co‐existing lesions to date. The serine/threonine‐protein kinase B‐Raf (BRAF) V600E mutation has been found at a high frequency of 54% in epithelioid glioblastomas. We present a case of a 26‐year‐old female patient with an epithelioid glioblastoma with the BRAF V600E mutation in her right frontal lobe. In the present case, a low‐grade diffuse astrocytoma component had colocalized with the epithelioid glioblastoma. The component presented prominent calcification on neuroimages as well as by histology, and low‐grade diffuse astrocytoma was considered to be a precursor lesion of an epithelioid glioblastoma. However, the BRAF V600E mutation was detected only in epithelioid glioblastoma but not in low‐grade diffuse astrocytoma. To the best of our knowledge, this is the first report demonstrating a discrepancy in the BRAF V600E mutation states between epithelioid glioblastoma and colocalized low‐grade astrocytoma. 相似文献
85.
86.
Kokichi Sugano Seigo Nakamura Jiro Ando Shin Takayama Hiroyuki Kamata Isao Sekiguchi Megumi Ubukata Tetsuro Kodama Masami Arai Fujio Kasumi Yasuo Hirai Tadashi Ikeda Hiromitsu Jinno Masaki Kitajima Daisuke Aoki Akira Hirasawa Yuko Takeda Kumiko Yazaki Takashi Fukutomi Takayuki Kinoshita Ryuichiro Tsunematsu Teruhiko Yoshida Masako Izumi Shino Umezawa Hiroshi Yagata Hiroko Komatsu Naoko Arimori Noriko Matoba Nobuhisa Gondo Shiro Yokoyama Yoshio Miki 《Cancer science》2008,99(10):1967-1976
The prevalence of BRCA1/2 germline mutations in Japanese patients suspected to have hereditary breast/ovarian cancer was examined by a multi‐institutional study, aiming at the clinical application of total sequencing analysis and validation of assay sensitivity in Japanese people using a cross‐sectional approach based on genetic factors estimated from personal and family histories. One hundred and thirty‐five subjects were referred to the genetic counseling clinics and enrolled in the study. Full sequencing analysis of the BRCA1/2 gene showed 28 types of deleterious mutations in 36 subjects (26.7%), including 13 types of BRCA1 mutations in 17 subjects (12.6%) and 15 types of BRCA2 mutations in 19 subjects (14.1%). Subjects were classified into five groups and 22 subgroups according to their personal and family history of breast and/or ovarian cancer, and the prevalence of deleterious mutations was compared with previously reported data in non‐Ashkenazi individuals. Statistical analysis using the Mantel‐Haenszel test for groups I through IV revealed that the prevalence of Japanese subjects was significantly higher than that of non‐Ashkenazi individuals (P = 0.005, odds ratio 1.87, 95% confidence interval 1.22–2.88). Family history of the probands suffering from breast cancer indicated risk factors for the presence of deleterious mutations of BRCA1/2 as follows: (1) families with breast cancer before age 40 within second degree relatives (P = 0.0265, odds ratio 2.833, 95% confidence interval 1.165–7.136) and (2) families with bilateral breast cancer and/or ovarian cancer within second degree relatives (P = 0.0151, odds ratio 2.88, 95% confidence interval 1.25–6.64). (Cancer Sci 2008; 99: 1967–1976) 相似文献
87.
This study investigated whether a circadian variation is present in the sensitivity of platelets to nitric oxide (NO) and, if so, if long-term smoking modifies it. Blood samples were taken at 0:00, 6:00, 9:00, 12:00, and 18:00 from 14 nonsmokers and 10 smokers. Dose-response curves for platelet aggregation by collagen were constructed in both the presence and absence of 1.0 micro M of NOR-3, a NO donor. The antiaggregation properties of NOR-3 were quantified by the half maximal concentration (EC50) ratio in the presence of NOR-3 to that in its absence. Platelet aggregation showed a monophasic circadian rhythm, with the lowest levels at 6:00 and the highest at 18:00 in both groups. However, there was a significant (p < 0.01) upward shifting of platelet aggregation in the smokers. A circadian variation in sensitivity to NOR-3 also was demonstrated in the nonsmokers. The sensitivity was lowest at 6:00 (1.68 +/- 0.19), increased significantly at 9:00 (2.58 +/- 0.26; p < 0.01), and remained high at 12:00 (2.47 +/- 0.21; p < 0.05). In smokers, however, a circadian variation in platelet sensitivity to NOR-3 was not found. Furthermore, the sensitivity was significantly lower at 9:00 and 12:00 in smokers (1.94 +/- 0.26 and 1.76 +/- 0.13, respectively; p < 0.05 for both) than in nonsmokers. Thus, long-term smoking impairs the normal morning increase in platelet sensitivity to NO, making platelets in smokers more thrombogenic during the hazardous hours. 相似文献
88.
89.
90.
Yamamoto G Tanaka A Tsuda Y Shimada T Nishida T Nishikawa M Inoda H Takigami K Yoshitake K 《Gan to kagaku ryoho. Cancer & chemotherapy》2002,29(13):2533-2536
We encountered a case of extensive squamous cell carcinoma ranging from the tongue to the mouth floor, in which chemotherapy using a combination of nedaplatin and 5-FU was effective. The patient was a 46-year-old male, who noticed a small mass in the mouth floor in September 2000, and visited the department of oral and maxillofacial surgery at a hospital on October 12, 2000. A 27 x 15 mm tumor with erosion was noted on the mouth floor, which was diagnosed as squamous cell carcinoma by biopsy, and the patient was referred to our department for treatment on November 16, 2000. Intra-oral findings included a healthy-colored induration with a bulge in the area ranging from the apex of the tongue posteriorly for 30 mm, and from the right lateral edge of the tongue to the left side exceeding the median area of the tongue by approximately 7 mm. MRI detected a tumor of approximately 2 cm in diameter in the area ranging from the median area of the tongue to the right ventral side of the tongue, which protruded on the mouth floor side. Two courses of combination chemotherapy using nedaplatin and 5-FU were performed. Nedaplatin (90 mg/m2, total 143 mg) and 5-FU (700 mg/m2, total 1,113 mg) were administered in a first course during December 15-19, 2000, and in the same amounts in a second course during January 23-27, 2001. Adverse effects of gastralgia and stomatitis occurred, but they gradually disappeared with time. The tumor with erosion in the tongue and mouth floor and induration disappeared 2 weeks after administration. Tongue was recovered, so that tongue movement was almost normal. Postoperative MR showed no abnormal signals in T2-weighed images, suggesting that the tumor in the right mouth floor had almost disappeared. External irradiation (40 Gy/20 times/28 days, 2 Gy/day, opposing bilateral portal irradiation) between March 13 and April 9, 2001, and micro-selection high dose fractionated interstitial irradiation (42 Gy/7 times/6 days, 6 Gy/1 time) April 18-23, 2001 were performed as booster therapy. Outpatient observation has shown a good clinical course without recurrence. 相似文献