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991.
992.
Kozo Fujita M.D Toshiaki Oka M.D Yutaka Suzuki M.D Shigeo Shimizu M.D Yoshiya Ito M.D Hitoshi Kakehashi M.D Hajime Yoshioka M.D. 《Pediatrics international》1991,33(2):191-194
A fatal case of leukemia complicated by mixed invasive aspergillosis and candidiasis is presented. Mixed fungal infections may occur in any immunocompromised patients. We should be careful to look for different morphologies of fungi in diagnostic examinations of lesions in these patients. 相似文献
993.
目的 :探讨痔周围血管半环形断流术 (SDH)预防痔术后大出血的价值。方法 :将 35 4例 — 期内痔及混合痔患者随机分为 2组 ,治疗组 (170例 )采用 SDH,对照组 (184例 )采用传统式外剥内扎术。观察术后创面出血率、创面愈合时间、症状消失率及复发率。结果 :治疗组与对照组在术后出血率、创面愈合时间及复发率方面差异有显著性统计学意义 (P<0 .0 5 )。而在症状消失率方面差异无显著性统计学意义 (P >0 .0 5 )。结论 :SDH是预防痔术后大出血的有效方法 ,同时能缩短切口愈合时间和降低复发率 相似文献
994.
The effect of the dopamine agonist antidepressant drug, nomifensine, on mixed anxiety/depressive states in general practice was assessed by means of a double-blind comparison with a standard fluphenazine/nortriptyline preparation. 57 patients were randomly allocated to 4 weeks' treatment with either nomifensine 25-50 mg taken three times daily, or a tablet containing 1.5 mg fluphenazine with 30 mg nortriptyline (Motipress) taken once daily. The overall response to both treatments was satisfactory, but Motipress was significantly superior (P less than 0.01) to nomifensine in the relief of fatigue and loss of energy, irritability, poor concentration and difficulty in coping, and there was also evidence of greater relief of depressive symptoms. In mixed anxiety/depressive states in general practice, nomifensine offers no advantage over a simple one tablet daily Motipress regimen. 相似文献
995.
We have previously shown that depletion of central nervous system (CNS) catecholamines by injecting the neurotoxin 6-hydroxydopamine (6-OHDA) into the cisterna magna of C57B1/6 mice markedly impairs the humoral immune response to sheep red blood cells. This work extends these observations by showing that 6-OHDA treatment also inhibits the humoral antibody response to the T-cell-dependent antigen trinitrophenyl-keyhole limpet hemocyanin, but does not affect the response to the T-independent antigen trinitrophenyl-lipopolysaccharide. This treatment also impairs humoral responsiveness at peripheral lymphoid sites in addition to inhibiting natural killer cell activity. However, 6-OHDA treatment in vivo does not affect in vitro mixed lymphocyte responsiveness, mitogen-induced lymphocyte activation or antigen presentation by macrophages. 相似文献
996.
Antisperm antibodies in split ejaculates. 总被引:2,自引:0,他引:2
The split ejaculation technique concentrates the most motile and viable spermatozoa in the first part of the ejaculate. Several clinicians use this fraction for insemination and in vitro fertilization. Eleven vasovasostomized men with antisperm antibodies participated in this study. The mixed antiglobulin reaction (MAR) for IgG, IgA, and secretory component was carried out on the whole ejaculate and the fractions of the split ejaculate. The isotype and concentration of free antisperm antibodies were determined in serum, the whole ejaculate and the fractions of the split ejaculate by the indirect MAR and the tray agglutination test. The detection of bound antisperm antibodies revealed almost identical reactions in fractions one and two and in the whole ejaculate. The results suggested that the majority of antisperm antibodies in the ejaculate from vasovasostomized men are transuded from serum not only at the epididymal and/or the prostatic level but also in the seminal vesicles. 相似文献
997.
T. Kumabe Teiji Tominaga Takashi Yoshimoto Takamasa Kayama 《Child's nervous system》1997,13(3):178-181
A case of sequential occurrence of multiple intracranial mixed germ cell tumors is presented. An 8-year-old boy with a cystic
calcified tumor in the basal ganglia and an increased serum α-fetoprotein concentration was initially treated with radiotherapy.
Six years later, a tumor composed of embryonal carcinoma and immature teratoma arose from the right temporo-parietal lobe.
This tumor was treated successfully with surgery and radiochemotherapy. The possibility of multicentricity or intra-axial
metastasis distant from the original site during the long-term course should be considered in treatment for intracranial germ
cell tumors.
Received: 6 November 1995 Revised: 17 July 1996 相似文献
998.
999.
Summary A case of thrombotic thrombocytopenic purpura (TTP) occurring in a patient with mixed connective tissue disease (MCTD) is reported. 相似文献
1000.
F. Lampert J. Harbott W. -D. Ludwig C. -R. Bartram J. Ritter V. Gerein M. Neidhardt R. Mertens N. Graf H. Riehm 《Annals of hematology》1987,54(6):325-335
Summary Clinical and laboratory features of seven patients with acute leukemia associated with the (4; 11) chromosome translocation are presented. Leukemic blasts of these patients showed lymphoid morphology in 6 (although 1 was treated for monoblastic leukemia 3 years earlier) and monocytoid morphology in 1, were positive for TdT and HD 37 (CD 19) in 6 patients, whereas weak expression of CALLA was seen in only 1 patient and T-lineage-associated antigens in none. Leukemic blasts from four patients showed the simultaneous expression of B-lymphoid and myeloid antigens, suggesting leukemogenesis in a very early multipotent progenitor cell. In 2 patients an isochromosome of the long arm of No. 7 chromosome was found in the leukemic karyotypes in addition to t (4; 11) (q21; q23); in one instance present at diagnosis, in the other one occurring at relapse. In one other patient leukemia karyotype also demonstrated trisomy 8. Leukemic cells of three patients were investigated by molecular genetics and demonstrated immunoglobulin gene rearrangements for the Ig heavy chain sequences but not for the light chain constant regions and T cell receptor sequences. All patients were treated by intensive chemotherapy. Four of the 7 patients are in continuous complete remission. The longest event-free survival time (over 2 1/2 years) was seen in one patient who had also DOWN-syndrome. Including these 7 patients a clinical analysis of 71 patients with t (4; 11) acute leukemia was made, emphasizing the following characteristics at diagnosis: female sex (62%), age under 2 years (49%), leukocyte count over 100×109/1 (61%), splenomegaly (80%), CNS-disease (11%). Survival of over 2 years was reported in less than 15% of the patients. It remains to be seen if risk-adapted treatment can alter the course of this early B-precursor acute leukemia with hitherto very bad prognosis. 相似文献