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51.
乳腺囊性增生病癌变过程中部分因素变化的意义 总被引:3,自引:0,他引:3
检测乳腺囊性增生病(FCD)经不典型增生到癌变部分因素的变化。结果提示:从因明显FCD症状活检至癌变为2~10年;从Ⅱ级以上不典型增生到临床癌变需2~7年;癌变率为3.1%。FCD患者存在性激素分泌调控失常,血浆雌激素和催乳素含量增加,导致上皮细胞增生。乳腺一般性增生细胞的DNA含量和超微结构与正常乳腺上皮细胞相似;无肿瘤相关抗原及异常基因产物表达。而发生在一般性增生基础上的不典型增生则呈现细胞基因物质DNA含量增加,部分为超4C的多倍体细胞;同时出现细胞膜和细胞核超微结构异常;雌激素受体含量增加,对性激素的依赖性和敏感性增强;部分不典型增生细胞出现胚胎性肿瘤相关抗原和异常基因产物表达。随不典型增生程度加重至乳腺癌,上述诸因素的变化趋势具有明显规律性。提示FCD上皮细胞从一般性增生经不典型增生至乳腺癌为细胞生物学连续逐渐变化的过程。部分不典型增生细胞中具有癌倾向的细胞生物学行为异常和表型变化与乳腺癌发生密切相关。细胞核DNA含量等异常变化及程度可作为乳腺癌前病变发展程度的客观标志 相似文献
52.
超声引导下肿瘤内注射^90钇玻璃微球的肝癌综合治疗 总被引:12,自引:0,他引:12
超声引导下对28例肝癌病人进行了肿瘤内注射^90钇玻璃微球(Y-90GT MS)为主的综合性治疗(部分病人配合肿块周边注射无水酒精及门静脉穿刺化疗)。随访2~16个月(平均7.9个月),病人全健在。肿瘤缩小率为91%,其中显著缩小达75%;肿块回声呈致密增强,少数呈混合型或等回声型;肿瘤内及周边血流信号显著减少;原甲胎蛋白升高者13例,11例显著下降,其中6例降至正常;病人症状减轻,全身情况改善。 相似文献
53.
Elchanan Nussinson Lica Vigder M.D. Zvi Kaveh Haim Gutman Philip Trougouboff Nathan Tzur 《Abdominal imaging》1988,13(1):306-308
A case of subserosal gastric neurilemmoma is hereby presented. This reported case is unique in its clinical presentation including the appearance of acute abdomen and fever subsequent to unremarkable and uneventful upper gastrointestinal endoscopy. The tendency of neurilemmoma to cause mucosal ulceration with fistula formation probably led to this clinical presentation. The role of computed tomography in establishing diagnosis of exogastric tumor is emphasized. 相似文献
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55.
R Rupprecht A Lippold C Auras G Bramkamp C Breitkopf H-J Elsmann EM Habenicht V Jasnoch H Müller-Pannes K-W Schulte L Suter 《Journal of the European Academy of Dermatology and Venereology》2007,21(2):178-185
Background Cosmetic changes are to be expected after radiotherapy for skin tumours. Objectives This study aimed to answer the questions: How frequent are cosmetic changes after soft X‐ray therapy? Do treatment parameters, tumour thickness, localization and size of the irradiated field have a major influence? Were patients irritated by the visual appearance of the irradiated field? Methods In total, 2474 examinations of 1149 irradiated fields were performed. Results Hypopigmentation was found in 64.7% of examinations more than 90 days after therapy, teleangiectases in 43.1%, erythema in 24.8%, and hyperpigmentation in 16.8%. The frequency of hypopigmentation, teleangiectases and hyperpigmentation increased with time from X‐ray exposure; more than 4 years after therapy hypopigmentation was diagnosed in 91.8% and teleangiectases in 82.2% of examinations. Total dose, the time–dose–fractionation factor (TDF), field size and dose per fraction were significantly related to the frequency of cosmetic changes. Incidence rates of cosmetic changes differed by less than 15% if different treatment conditions were compared: thicker vs. thinner tumours, larger vs. smaller fields, higher vs. lower total doses, doses per fraction, and TDF. Frequencies of hypopigmentation, teleangiectases, erythema and hyperpigmentation differed by more than 15% between some localizations on the head. Women reported irritation by the visual appearance of the irradiated field in 12.6% of 1116 interviews, and men in 4.4% of 1284 interviews. Conclusions Cosmetic changes after soft X‐ray therapy are relatively frequent. Treatment parameters, tumour thickness and field size have only a minor influence. Few patients, but more women than men, were irritated by the visual appearance of the irradiated field. 相似文献
56.
S. Loughran N. Calder F.B. MacGregor P. Carding K. MacKenzie 《Clinical otolaryngology》2005,30(1):42-47
Objectives: To assess whether proposed voice and quality of life (QoL) outcome measures were likely to be acceptable to patients previously treated for early glottic cancer by either radiotherapy or endoscopic resection, as well as looking for differences in QoL and voice between treatments. Design: Questionnaire‐based cohort study. Setting: Secondary care, three centres. Participants: All patients treated for T1a or in situ glottic carcinoma between 1997 and 2003. Fifty‐three patients were identified; those who had undergone salvage surgery or radiotherapy were excluded. A proportion refused to participate or could not be contacted and two patients had died of unrelated causes. Thirty‐six patients completed the trial with 18 from each treatment arm. Main outcome measures: Quality of voice as assessed by three questionnaires, Voice Handicap Index (VHI), Vocal Performance Questionnaire (VPQ), Voice Symptom Score (VoiSS) and perceptual analysis of voice by Grade, Roughness, Breathiness, Asthenia and Strained (GRBAS) assessment of vocal recordings. Quality of life as assessed by the Hospital Anxiety and Depression Scale (HADS), University of Washington Quality of Life Questionnaire (UW‐QoL), and the Functional Assessment of Cancer Therapy (FACT) questionnaire. Results: All patients included in the trial were able to complete the questionnaires; however, 19% required assistance of some kind. GRBAS assessment showed no difference between groups for any criteria. All QoL questionnaires gave equivalent good scores. All of the voice questionnaires showed no statistical difference between groups except for the emotional subscale of the VoiSS which showed a significantly better score for the radiotherapy arm (P = 0.04). Conclusion: All outcome measures were applicable and acceptable to the patient group. Overall QoL and voice appears similar despite treatment arm, apart from the emotional subscale of the VoiSS. A randomized controlled trial is required to further assess this question. 相似文献
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59.
Syndecan-1和E-candherin在声门上型喉鳞状细胞癌中的表达及意义 总被引:2,自引:0,他引:2
目的:探讨Syndecan—1和E—candherin两种黏附分子在声门上型喉鳞状细胞癌中的表达情况及与喉癌生物学行为之间的关系。方法:应用SP免疫组织化学法检测了38例声门上型喉鳞状细胞癌和7例喉黏膜慢性炎症组织中的Syndecan-1和E—candherin的表达并根据阳性瘤细胞占肿瘤细胞总数的比率进行半定量分析和统计检验。结果:Syndecan-1和E—candherin的阳性染色部位主要集中于细胞膜,E—candherin也可表达于细胞间质。Syndecan-1和E-candherin在恶性程度高的癌细胞上膜表达明显缺失,并与组织学分化、肿瘤大小密切相关。Syndecan-1和E-candherin在喉鳞状细胞癌细胞上的表达结果有相关性,但无敏感性差异。结论:Syndecan-1和E-candherin的表达可能在声门上型喉鳞状细胞癌的发生发展等生物学行为中起着重要的作用。 相似文献
60.
18例原发鼻腔和鼻窦的T/NK淋巴瘤的临床分析 总被引:5,自引:3,他引:2
目的:探讨原发于鼻腔和鼻窦的T/NK恶性淋巴瘤的临床特点。方法:对18例患者的临床资料进行回顾性分析。结果:鼻腔和鼻窦的T/NK淋巴瘤首发症状不典型,多为鼻塞、涕血、局部肿胀及发热等,临床误诊率高;高分期及高侵袭性淋巴瘤预后差。结论:鼻腔鼻窦的T/NK淋巴瘤是结外非霍奇金恶性淋巴瘤(NHL)的一个独特类型,首发症状多样,临床上应注意对该病的认识,防止误诊;预后有赖于病理分型和临床分期。 相似文献