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1.
《Vaccine》2022,40(19):2679-2695
Vaccinations are essential for preventing infectious diseases in children with chronic diseases as they have increased risk of infection from frequent use of biologics. Response to immunizations in this group is not well known.ObjectiveA systematic review was performed to evaluate three primary outcomes: efficacy; immunogenicity; and safety of vaccines in children with chronic conditions treated with biologics.MethodsThe protocol for our systematic review and meta-analysis was registered and published with PROSPERO. We searched electronic bibliographic databases for studies published from 2009 to 2019, focusing on vaccinations in children with chronic conditions treated with biologics.ResultsWe retrieved 532 records. Thirty-one full-text articles were selected, and 14 were included in the meta-analysis. No significant publication bias was found. Efficacy: limited data are available regarding the efficacy of vaccination, as most studies have focused on immunogenicity as surrogate outcome for efficacy. Immunogenicity: patients receiving anti-TNF-alpha therapy had a statistically significant risk of poor seroconversion (p = 0.028) and seroprotection by the serotype B influenza vaccine [inflammatory bowel disease (IBD) p = 0.013; juvenile idiopathic arthritis (JIA) p = 0.004]. We found adequate responses with H1N1 and H3N2 serotypes. Few studies existed for pneumococcal, hepatitis A virus, hepatitis B virus, varicella-zoster virus, Measles Mumps Rubella virus, and multiple vaccine administration. Safety: vaccine administration was not associated with serious side effects, but JIA patients on anti-TNF alpha therapy had a statistically significant risk of presenting with myalgia or arthralgia postinfluenza vaccine (p = 0.014).ConclusionsMore evidence concerning efficacy, immunogenicity, and safety of vaccinations is needed to guide physicians in the vaccine decision process for this pediatric population. 相似文献
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Cutaneous histiocytoses constitute a heterogeneous group of diseases characterised by the cutaneous accumulation of cells with the cytological and phenotypic features of macrophages or dendritic cells. The clinical spectrum ranges from self-resolving, skin-limited conditions to severe, multiorgan disease with a high morbidity rate. Until recently, cutaneous histiocytoses were classified according to the immunophenotype of the pathological cells, with differentiation between Langerhans cell histiocytosis (LCH) [CD1a+, CD207 (langerin)+] and non-Langerhans cell histiocytosis (CD68+, CD163+, CD1a?, CD207?). Over the last 12 years, a number of new pathophysiological findings (in particular, molecular pathology results) regarding histiocytoses have contributed to a new classification based on molecular alterations, as well as on clinical and imaging characteristics and the phenotype. The most frequent entities in children are juvenile xanthogranuloma and LCH. 相似文献
3.
全身型幼年特发性关节炎是儿童常见的风湿性疾病之一, 肺间质病变是指以肺间质和远端气隙重构为特征, 进而导致异常气体交换的疾病。近年来, 国内外对全身型幼年特发性关节炎合并肺间质病变的报道有增多趋势。该文总结了近年来报道中全身型幼年特发性关节炎儿童合并肺间质病变的情况, 并对儿童肺间质病变的临床表现, 影像学表现, 诊断和治疗进行综述,旨在对该类疾病有更深刻的认识, 有助于肺间质病变的早期诊治。 相似文献
4.
全身型幼年特发性关节炎(sJIA)临床表型不一,以发热为突出表现,伴或不伴有关节炎、皮疹等特点,临床缺乏基于证据的指南,全球在 sJIA 治疗方面存在很大差异。该文总结了sJIA 的传统药物(非甾体抗炎药、糖皮质激素、改善病情抗风湿药)、新兴生物制剂的治疗要点,以及近年来国内外关于sJIA治疗的推荐,并对目前关心的药物减停及疾病长期管理问题进行探讨,旨在对sJIA达标治疗的理念有更深入的认识,从而规范治疗策略、改善临床预后。 相似文献
5.
Herbert Schulz Ann‐Kathrin Ruppert Federico Zara Francesca Madia Michele Iacomino Maria S. Vari Ganna Balagura Carlo Minetti Pasquale Striano Amedeo Bianchi Carla Marini Renzo Guerrini Yvonne G. Weber Felicitas Becker Holger Lerche Claudia Kapser Christoph J. Schankin Wolfram S. Kunz Rikke S. Mller Karen L. Oliver Susannah T. Bellows Saul A. Mullen Samuel F. Berkovic Ingrid E. Scheffer Hande Caglayan Ugur Ozbek Per Hoffmann Sara Schramm Despina Tsortouktzidis Albert J. Becker Thomas Sander 《Epilepsia》2019,60(5):e31-e36
Juvenile myoclonic epilepsy (JME) is a common syndrome of genetic generalized epilepsies (GGEs). Linkage and association studies suggest that the gene encoding the bromodomain‐containing protein 2 (BRD2) may increase risk of JME. The present methylation and association study followed up a recent report highlighting that the BRD2 promoter CpG island (CpG76) is differentially hypermethylated in lymphoblastoid cells from Caucasian patients with JME compared to patients with other GGE subtypes and unaffected relatives. In contrast, we found a uniform low average percentage of methylation (<4.5%) for 13 CpG76‐CpGs in whole blood cells from 782 unrelated European Caucasians, including 116 JME patients, 196 patients with genetic absence epilepsies, and 470 control subjects. We also failed to confirm an allelic association of the BRD2 promoter single nucleotide polymorphism (SNP) rs3918149 with JME (Armitage trend test, P = 0.98), and we did not detect a substantial impact of SNP rs3918149 on CpG76 methylation in either 116 JME patients (methylation quantitative trait loci [meQTL], P = 0.29) or 470 German control subjects (meQTL, P = 0.55). Our results do not support the previous observation that a high DNA methylation level of the BRD2 promoter CpG76 island is a prevalent epigenetic motif associated with JME in Caucasians. 相似文献
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Suvi Renkonen Lars‐Olaf Cardell Petri Mattila Marie Lundberg Caj Haglund Antti A. Mäkitie 《APMIS : acta pathologica, microbiologica, et immunologica Scandinavica》2015,123(5):439-444
Juvenile nasopharyngeal angiofibroma (JNA) is a rare, benign tumor affecting adolescent males. The etiology of JNA as well as the causes determining the variable growth patterns of individual tumors remains unknown. Toll‐like receptors (TLRs) are part of the innate immune response to microbes; by recognition of distinct features, they link to induction of pro‐inflammatory signaling pathways. We immunostained TLR 3, 7, and 9 in 27 JNA specimens of patients treated at the Helsinki University Central Hospital, Helsinki, Finland, during the years 1970–2009. Results: TLR 3, 7, and 9 expressions were found in stromal and endothelial cells of JNA, and their expression levels varied from negative to very strong positive. TLR 3 expression was found to have a significant correlation with the clinical stage of JNA. Conclusions: The present results propose a putative role of TLRs in the growth process of JNA. 相似文献
9.
《Actas dermo-sifiliográficas》2020,111(9):725-733
Juvenile xanthogranulomas (JXGs) are rare, benign lesions that belong to the large group of non-Langerhans cell histiocytoses. JXG presents with 1 or more erythematous or yellowish nodules that are usually located on the head or neck. Most JXG lesions are congenital or appear during the first year of life. Extracutaneous involvement is rare, but the literature traditionally suggests investigating the possibility of ocular compromise. JXG is mainly a clinical diagnosis, but a skin biopsy may sometimes be needed for confirmation. JXGs on the skin are self-limiting and usually do not require treatment. This review describes the clinical and therapeutic aspects of JXG, emphasizing available evidence and the diagnosis of extracutaneous involvement. 相似文献