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101.
Pierre Tachon Radovan Borojevic 《Transactions of the Royal Society of Tropical Medicine and Hygiene》1978,72(6):605-609
Reaction to schistosomal antigen was studied in children born to mothers infected with Schistosoma mansoni. Values of immediate (15 min) skin reactions were more elevated and values of delayed (24 h) skin reactions were significantly higher in children born to infected mothers than in children born to un-infected mothers. The macrophage migration inhibition test, done on cord blood cells, was positive to schistosomal antigen in 40% of children born to infected mothers and negative in all children born to uninfected mothers. These results suggest prenatal sensitization to schistosomal antigen in children born to mothers infected with S. mansoni. 相似文献
102.
Radovan Vanatka Cécile Rouzier Jean Claude Lambert Carole Leroux Alain Coussement 《Skeletal radiology》2011,40(3):347-351
Winchester syndrome (WS) is a rare autosomal recessive syndrome resulting in multicentric osteolysis. Only a few cases of
WS have been described in the literature worldwide. It has recently been shown to be caused by mutation in the gene encoding
matrix metalloproteinase-2 (MMP2). We report a patient affected by WS with a proven mutation of the MMP2 gene and describe
the progression of radiological findings over a 23-year period. To our knowledge there is no comparable article concerning
the WS in the literature. 相似文献
103.
Absence of N-RAS point mutations in peripheral blood cells of patients with aplastic anaemia and paroxysmal nocturnal haemoglobinurea 总被引:1,自引:0,他引:1
Jonathan R. White Klaus M. Josten Rima Chopra Jennifer Tooze Radovan Saso Edward C. Gordon-Smith Tim R. Rutherford 《British journal of haematology》1995,91(4):921-923
Summary. The myelodysplastic syndromes (MDS) have a significant frequency of evolution into acute myeloid leukaemia (AML). Approximately 30% of MDS patients show activating mutations of the N-RAS proto-oncogene, and these patients are at increased risk of leukaemic evolution. Long-term survivors of aplastic anaemia (AA) and paroxysmal nocturnal haemoglobinurea (PNH) are also at significant risk of developing AML. We have screened peripheral blood DNA from 42 AA patients and 15 PNH patients for the presence of N- RAS point mutations. No mutations were detected in these samples, indicating that the mechanisms of evolution into AML may be different from those in MDS. 相似文献
104.
Corinne De Lord Jennifer A. Tooze Radovan Saso Judith C. W. Marsh & Edward C. Gordon-Smith 《British journal of haematology》1998,101(1):90-93
Deficient expression of glycosylphosphatidyl inositol (GPI)-anchored proteins in aplastic anaemia (AA) patients has previously been reported to be associated with a poor response to immunosuppressive (IS) therapy. Here we report the response to IS therapy of 111 patients with AA and correlate this with GPI-anchored protein expression on peripheral blood cells by flow cytometry. A GPI-anchored protein deficient population was identified in 15% (17/111) of patients with AA who had a negative Ham's test and no laboratory evidence of haemolysis. Patients were treated with antilymphocyte globulin and/or cyclosporin A, or oxymetholone. Bone marrow transplantation was performed in 12 patients, seven of whom had not responded to IS therapy. In patients tested for GPI-anchored protein expression prior to IS therapy there was no difference in response rate to IS therapy between AA patients with a GPI-anchored protein deficiency and those with normal GPI-anchored protein expression (50% response rate versus 75%, respectively). Survival in these two groups was similar at 90% with follow-up over 140 months from diagnosis. Eight of the 17 AA patients who developed a GPI-anchored protein-deficient population later went on to develop a positive Ham's test. From this study we demonstrate a lower incidence of GPI-anchored protein deficiency in AA patients compared with previous reports. In addition we have shown that the presence of a GPI-anchored protein-deficient cell population in patients with AA who have a negative Ham's test is not a poor prognostic factor in terms of response and survival after IS therapy. 相似文献
105.
106.
Radovan Prikryl Miroslava Kholova Hana Prikrylova Kucerova Eva Ceskova 《Comprehensive psychiatry》2013
Objective
The aim of the study was to map the point prevalence of remission and recovery in patients with schizophrenia in the Czech Republic.Method
The point-symptomatic remission criteria were based on the definition of remission in schizophrenia according to Andreasen, without the time criterion. The definition of complete remission contained, in addition to the point-symptomatic remission criteria, a time aspect which was determined by the absence of psychiatric hospitalisation or a change in antipsychotic medications due to inefficiency in the preceding six months. Functional remission was defined by a total score on the PSP scale in the range between 71 and 100 points. Recovery was defined by the simultaneous fulfilment of the criteria for complete and functional remission.Results
A total of 481 patients with schizophrenia were included in the study. The point-symptomatic remission criteria were fulfilled in a total of 258 patients (54%); complete remission occurred in a total of 214 patients (44%). Functional remission was reached by 124 patients (26%) in total. Recovery was proven in a total of 91 patients (19%).Conclusion
The ascertained data are in accordance with the results of methodologically similar studies and confirm the known trajectories of the course of schizophrenia. 相似文献107.
Leandra S. Baptista Karina R. Silva Carolina S.G. Pedrosa Ronaldo J.F.C. Amaral João Vitor Belizário Radovan Borojevic José Mauro Granjeiro 《Artificial organs》2013,37(12):1068-1075
The objective of our study was to investigate chondrogenesis potential of human adipose‐derived mesenchymal stromal cells (MSCs), using as a positive control a human source of cartilage‐derived progenitor cells (PCs). This source of PCs was recently described by our group and dwells on the surface of nasoseptal cartilage. Histological analysis using Safranin O staining and immunofluorescence for actin filaments and collagen type II was performed on three‐dimensional (3D) pellet cultures. Cartilage PCs and adipose MSCs showed similarities in monolayer culture related to cell morphology and proliferation. Our 3D pellet cultures substantially reduced the actin stress and after 21 days under chondrogenic medium, we observed an increase in the pellet diameter for cartilage PCs (7.4%) and adipose MSCs (21.2%). Adipose‐derived MSCs responded to chondrogenic stimulus, as seen by positive areas for collagen type II, but they were not able to recreate a mature extracellular matrix. Using semi‐quantitative analysis, we observed a majority of Safranin O areas rising from blue (no stain) to orange (moderate staining) and no changes in fibroblastic morphology (P < 0.0001). For cartilage PCs, chondrogenic induction is responsible for morphological changes and a high percentage of matrix area/number of cells (P ≤ 0.0001), evaluated by computerized histomorphometry. Morphological analyses reveal that adipose‐derived MSCs were not able to recreate a bioengineered cartilage. The cost of culture was reduced, as the cartilage PCs under growth‐factor free medium exhibit a high score for cartilage formation compared with the induced adipose mesenchymal stromal cells (P = 0.0021). Using a pellet 3D culture, our cartilage PCs were able to produce a cartilage tissue in vitro, leading to the future development of bioengineered products. 相似文献
108.
109.
Stefan Kohl Daw-Yang Hwang Gabriel C. Dworschak Alina C. Hilger Pawaree Saisawat Asaf Vivante Natasa Stajic Radovan Bogdanovic Heiko M. Reutter Elijah O. Kehinde Velibor Tasic Friedhelm Hildebrandt 《Journal of the American Society of Nephrology : JASN》2014,25(9):1917-1922
Congenital anomalies of the kidney and urinary tract (CAKUT) account for approximately 40% of children with ESRD in the United States. Hitherto, mutations in 23 genes have been described as causing autosomal dominant isolated CAKUT in humans. However, >90% of cases of isolated CAKUT still remain without a molecular diagnosis. Here, we hypothesized that genes mutated in recessive mouse models with the specific CAKUT phenotype of unilateral renal agenesis may also be mutated in humans with isolated CAKUT. We applied next-generation sequencing technology for targeted exon sequencing of 12 recessive murine candidate genes in 574 individuals with isolated CAKUT from 590 families. In 15 of 590 families, we identified recessive mutations in the genes FRAS1, FREM2, GRIP1, FREM1, ITGA8, and GREM1, all of which function in the interaction of the ureteric bud and the metanephric mesenchyme. We show that isolated CAKUT may be caused partially by mutations in recessive genes. Our results also indicate that biallelic missense mutations in the Fraser/MOTA/BNAR spectrum genes cause isolated CAKUT, whereas truncating mutations are found in the multiorgan form of Fraser syndrome. The newly identified recessive biallelic mutations in these six genes represent the molecular cause of isolated CAKUT in 2.5% of the 590 affected families in this study. 相似文献
110.
Pavel Jurak Karol Curila Pavel Leinveber Frits W. Prinzen Ivo Viscor Filip Plesinger Radovan Smisek Radka Prochazkova Pavel Osmancik Josef Halamek Magdalena Matejkova Jolana Lipoldova Miroslav Novak Roman Panovsky Petr Andrla Vlastimil Vondra Petr Stros Jana Vesela Dalibor Herman 《Journal of cardiovascular electrophysiology》2020,31(1):300-307