全文获取类型
收费全文 | 106610篇 |
免费 | 7339篇 |
国内免费 | 2378篇 |
专业分类
耳鼻咽喉 | 1728篇 |
儿科学 | 3030篇 |
妇产科学 | 1822篇 |
基础医学 | 11437篇 |
口腔科学 | 3140篇 |
临床医学 | 8994篇 |
内科学 | 20290篇 |
皮肤病学 | 2838篇 |
神经病学 | 6252篇 |
特种医学 | 2928篇 |
外国民族医学 | 1篇 |
外科学 | 11731篇 |
综合类 | 10675篇 |
现状与发展 | 12篇 |
一般理论 | 21篇 |
预防医学 | 11434篇 |
眼科学 | 1748篇 |
药学 | 9167篇 |
53篇 | |
中国医学 | 4567篇 |
肿瘤学 | 4459篇 |
出版年
2024年 | 185篇 |
2023年 | 878篇 |
2022年 | 2293篇 |
2021年 | 3953篇 |
2020年 | 2463篇 |
2019年 | 2921篇 |
2018年 | 3420篇 |
2017年 | 2585篇 |
2016年 | 2321篇 |
2015年 | 3071篇 |
2014年 | 4386篇 |
2013年 | 5792篇 |
2012年 | 8419篇 |
2011年 | 8906篇 |
2010年 | 6351篇 |
2009年 | 5486篇 |
2008年 | 7038篇 |
2007年 | 6952篇 |
2006年 | 6357篇 |
2005年 | 5838篇 |
2004年 | 4911篇 |
2003年 | 4391篇 |
2002年 | 3805篇 |
2001年 | 2550篇 |
2000年 | 2478篇 |
1999年 | 1689篇 |
1998年 | 518篇 |
1997年 | 453篇 |
1996年 | 362篇 |
1995年 | 323篇 |
1994年 | 282篇 |
1993年 | 205篇 |
1992年 | 548篇 |
1991年 | 450篇 |
1990年 | 422篇 |
1989年 | 323篇 |
1988年 | 322篇 |
1987年 | 293篇 |
1986年 | 258篇 |
1985年 | 249篇 |
1984年 | 154篇 |
1983年 | 150篇 |
1982年 | 118篇 |
1981年 | 125篇 |
1980年 | 96篇 |
1979年 | 144篇 |
1978年 | 109篇 |
1974年 | 105篇 |
1971年 | 92篇 |
1969年 | 87篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
91.
制作角膜缘干细胞完全缺乏动物模型的新方法 总被引:2,自引:1,他引:1
目的提出一种新的角膜缘干细胞完全缺乏模型制作方法,为干细胞缺乏疾病的治疗性研究提供可靠的模型。方法利用9mm环钻划界,板层切除角膜组织,通过临床评分、印迹细胞学、组织病理及免疫组织化学验证模型的成功。结果板层切除术后30~45d,模型眼角膜混浊、上皮缺损、大量新生血管长入,印迹细胞学可见PAS( )的杯状细胞,组织病理学检查上皮符合结膜细胞表型,免疫荧光染色可见结膜杯状细胞特异性标志MUC5AC阳性表达。结论环钻划界加板层切除法为一种可靠、有效的角膜缘干细胞完全缺乏模型制作方法。 相似文献
92.
Marcondes C Fran?a Maria E Calcagnotto Jaderson C da Costa Iscia Lopes-Cendes 《Movement disorders》2006,21(7):1051-1053
Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal-dominant neurodegenerative disorders caused by mutations in two different genes. We identified mutations for SCA2 and SCA3 segregating simultaneously in a single Brazilian family. The index patient had SCA2, whereas her two second-degree cousins had SCA3. Disease was more rapidly progressive in the SCA2 patient, who presented severe brainstem and pancerebellar atrophy, as opposed to the two SCA3 patients, who had only mild cerebellar vermian atrophy. In such situations, molecular confirmation of all patients may avoid misdiagnosis of SCA subtypes and eventual errors in predictive testing of unaffected family members. 相似文献
93.
o. goetze a. b. nikodem j. wiezcorek † m. banasch h. przuntek † t. mueller † w. e. schmidt & d. woitalla † 《Neurogastroenterology and motility》2006,18(5):369-375
Predictors of gastric emptying (GE) in patients with idiopathic Parkinson's disease (PD) of a solid and liquid meal are not well defined. For measurement of GE 80 patients with PD were randomly assigned to receive either a solid meal (250 kcal) containing 13C-octanoate (n = 40) or a liquid meal (315 kcal) with 13C-acetate (n = 40). All patient groups were off medication affecting motility and were matched for age, gender, body mass index, disease duration and severity, using Unified Parkinson's Disease Rating Scale (UPDRS). Gastric emptying was compared with a healthy control group (n = 40). Multiple regression analysis was used to determine predictors of gastric emptying. Exactly 88% and 38% of PD patients had delayed GE of solids and liquids respectively. Solid and liquid emptying was similar in women and men. There were no differences in GE in PD patients < 65 years of age when compared with patients > or = 65 years. Multiple regression analysis showed that motor handicaps such as rigour and action tremor are independent predictors of solid GE (r = 0.68, P < 0.001). The severity of motor impairment, but not any other neurological symptom, as assessed by UPDRS is associated with gastroparesis in PD and solid emptying is more likely to be delayed. 相似文献
94.
95.
JAE YOUNG JOUNG DONG GOO KANG HYUCK-JAE CHOI WEON SEO PARK HO KYUNG SEO JIN SOO CHUNG KANG HYUN LEE 《International journal of urology》2006,13(11):1451-1453
Abstract Gastrointestinal stromal tumor (GIST) is a recently described mesenchymal tumor that can develop in any portion of the gastrointestinal tract. The occurrence of a GIST in the urinary tract is rare, but GIST can present as tumor of the urinary tract or invade the urinary tract. This is the first reported case of GIST in the ileal neobladder, which presented as a submucosal tumor. The patient underwent an open exploration and partial resection of the neobladder pouch. 相似文献
96.
目的 :探讨遏制急性胰腺炎向重症转化的非手术治疗策略。方法 :将4年间收治的286例轻型急性胰腺炎分为对照组和治疗观察组。对照组采取常规非手术治疗措施;观察组加用改善胰腺微循环,防治细胞钙超载和抑制胰酶的治疗方法。结果 :对照组144轻型有20例转化为重症胰腺炎,14例发生全身性并发症;观察组142例轻型有8例转化为重症,2例出现全身性并发症。观察组重症患者血C-反应蛋白和Balthazar CT严重度指数在治疗后各时点较对照组明显降低。结论 :在常规治疗的基础上加用改善胰腺微循环,防治细胞钙超载和抑制胰酶的治疗措施可能有助于阻止轻型急性胰腺炎向重症化发展。 相似文献
97.
a. lobrano k. blanchard t.l. abell a. minocha w. boone j. wyatt-ashmead † j. fratkin † c. subramony † a. wee jr ‡ g. di nardo § g. barbara § v. stanghellini § & r. de giorgio § 《Neurogastroenterology and motility》2006,18(2):162-167
BACKGROUND AND AIM: Severe dysautonomia may be secondary to viral infections, resulting in impaired autoimmune, cardiovascular, urinary and digestive dysfunction. Herein, we present a case of a 31-year-old white female patient who had severe gastroparesis related to autonomic failure following an episode of acute gastroenteritis. This seems to be the first report providing thorough assessment of the enteric and autonomic nervous system by analysis of full-thickness small intestinal biopsies, cardiovagal testing and autopsy. HOSPITAL COURSE: This patient affected by a severe gastroparesis was treated with antiemetics, prokinetics, analgesics and gastric electrical stimulation to control symptoms. Nutritional support was made using jejunal feeding tube and, in the final stage of disease, with total parenteral nutrition. Autonomic studies revealed minimal heart rate variability and a disordered Valsalva manoeuvre although the enteric nervous system and the smooth muscle layer showed a normal appearance. Hospital courses were complicated by episodes of bacteraemia and fungemia. Serum antiphospholipid antibodies were noted but despite anticoagulation, she developed a pulmonary embolism and shortly thereafter the patient died. Autopsy revealed acute haemorrhagic Candida pneumonia with left main pulmonary artery thrombus. Sympathetic chain analysis revealed decreased myelinated axons with vacuolar degeneration and patchy inflammation consistent with Guillain-Barre syndrome. The evaluation of the enteric nervous system in the stomach and small bowel revealed no evidence of enteric neuropathy or myopathy. CONCLUSION: A Guillain-Barre-like disease with gastroparesis following acute gastroenteritis is supported by physiological and autonomic studies with histological findings. 相似文献
98.
99.
Iron Fortification of Flours in Venezuela 总被引:1,自引:0,他引:1
This paper reviews a conference about the impact of the iron fortification program in Venezuela; it was presented at the Pan American Health Organization regional technical meeting: "Iron Fortification: Where Are We in Terms of Iron Compounds," held in Washington January 10–12, 2001. Some of the data presented were published in the American Journal of Clinical Nutrition , including stimulating results about the impact of fortification of precooked corn and white wheat flours, as well as the prevalence of anemia and iron deficiency in the Venezuelan population. This article reports results from three surveys carried out in 1997, 1998, and 1999 on the same age and socioeconomic group that had been evaluated in 1990, 1992, and 1994. This article also shows the impact of iron fortification programs and the influence of other factors on the prevalence of iron deficiency and anemia during the last 7 years. 相似文献
100.
小鼠不完全性脑缺血、再灌注时脑膜血流量的变化及尼莫地平的作用 总被引:5,自引:1,他引:4
目的:观察双侧颈总动脉阻断后脑血流的变化。方法:结扎双侧颈总动脉观察小鼠不完全性脑缺血及其再灌注时脑膜血流量的变化。结果:结扎颈总动脉后小鼠脑膜血流量在几秒钟内骤然下降,血流量较结扎前降低约85.9%±6.45%。同时血管中红细胞运动近停滞状态,血管再通时脑血流处于低灌注状态,血流量下降34.47%±11.69%,此时脑缺血再灌后脑组织实际上处于一种慢性缺血状态。再灌注10d后,小鼠脑海马CA1区神经细胞数明显减少。尼莫地平可以解除再灌注时的脑血流低灌状态。并防止由此所引起的脑海马CA1区神经细胞的缺失。结论:缺血后及时给予尼莫地平具有积极的治疗意义。 相似文献