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81.
PM Braillon AL Guibal P Pracros-Deffrenne A Serban JP Pracros P Chatelain 《Acta paediatrica (Oslo, Norway : 1992)》1998,87(9):924-929
Ninety five normal Caucasian subjects (51F, 44 M) aged from 2 to 25 y were measured at the hand and wrist level with a small DXA system (pDEXA™) in order to obtain the normal values of the bone mineral content (BMC), density (BMD) and projected area (A) of carpal (c) and metacarpal (m) bones. BMDc ranged from 0.065 ± 0.007 g/cm to 0.365 ± 0.035 g/cm in females and 0.425 ± 0.040 g/cm in males. It presented a sharp change of increase rate at 15.5 and 17 y of age in girls and boys, respectively. Ac presented the same kind of evolution as BMDc, but had a larger value dispersion. The second metacarpal bone had the highest BMCm value in 85% of females and 90% of males. The sum of BMCmi or Ami values (i = 1–5) and the projected mean density of the 5 metacarpal bones was well correlated with BMCc, Ac and BMDc, respectively ( r > 0.90). A volumetric mineral density, dmi, calculated for each of these bones, approximated to a cylinder, was correlated with age ( r > 0.85). 相似文献
82.
83.
Gamma-carboxylated isoforms of recombinant human protein S with different biologic properties 总被引:3,自引:0,他引:3
Grinnell BW; Walls JD; Marks C; Glasebrook AL; Berg DT; Yan SB; Bang NU 《Blood》1990,76(12):2546-2554
Human protein S (HPS), a regulator of hemostasis, is a vitamin K- dependent plasma protein with potential clinical utility. We have obtained high-level expression of the cDNA for HPS in two mammalian cell lines. Both cell lines secreted single chain recombinant HPS (rHPS) in serum-free medium as determined by Western blot analysis. The ability of the rHPS from both cell lines to act as a cofactor for human protein C (HPC) was determined; the rHPS secreted from the human 293 cell line had an activity six times that of the rHPS from the AV12-664 Syrian hamster cell line. Furthermore, the relative specific cofactor activity of rHPS from the 293 cell line was actually 2.5-fold higher than that of single-chain human plasma-derived HPS. Essentially all of the rHPS secreted from the 293 cell line exhibited a calcium-dependent elution profile on anion exchange chromatography, whereas only 25% to 35% of the hamster cell-derived rHPS exhibited this profile. However, the calcium-eluted rHPS from the AV12 cell line had a high specific cofactor activity, equivalent to that of the 293-derived rHPS. A NaCl- elutable rHPS fraction (calcium nondependent) was isolated from the recombinant AV12-664 cell line, further purified, and found to have reduced activity, only 40% that of the calcium-dependent rHPS. The only observable difference in the calcium-dependent and nondependent rHPS molecules was in the content of gamma-carboxyglutamic acid (Gla); the calcium-dependent material contained approximately 10 mol Gla/mol protein whereas the calcium-nondependent material contained only approximately 8 mol Gla/mol of protein. In addition, the calcium- nondependent rHPS had reduced ability to interact with phospholipid vesicles as evidenced by an eightfold increase in the apparent kd. Our data demonstrate the isolation of rHPS with high specific activity, and show that a reduction in as few as two Gla residues dramatically decreases its functional cofactor activity for HPC, due to a reduction in ability to interact with the phospholipid bilayer. 相似文献
84.
85.
V.K. de Sá T.P. Rocha AL. Moreira F.A. Soares T. Takagaki L. Carvalho A.G. Nicholson V.L. Capelozzi 《Brazilian journal of medical and biological research》2015,48(11):1039-1047
We collected a series of 136 lung/bronchial and 56 matched lung parenchyma tissue
samples from patients who underwent lung/bronchial biopsies and presented invasive
carcinoma after lung surgery. The lung/bronchial samples included basal cell
hyperplasia, squamous metaplasia, moderate dysplasia, adenomatous hyperplasia, severe
dysplasia, squamous cell carcinoma and adenocarcinoma. Matched lung parenchyma tissue
samples included 25 squamous cell carcinomas and 31 adenocarcinomas.
Immunohistochemistry was performed to analyze for the distribution of hyaluronidase
(Hyal)-1 and −3, and hyaluronan synthases (HAS)-1, −2, and −3. Hyal-1 showed
significantly higher expression in basal cell hyperplasia than in moderate dysplasia
(P=0.01), atypical adenomatous hyperplasia (P=0.0001), or severe dysplasia (P=0.03).
Lower expression of Hyal-3 was found in atypical adenomatous hyperplasia than in
basal cell hyperplasia (P=0.01) or moderate dysplasia (P=0.02). HAS-2 was
significantly higher in severe dysplasia (P=0.002) and in squamous metaplasia
(P=0.04) compared with basal cell hyperplasia. HAS-3 was significantly expressed in
basal cell hyperplasia compared with atypical adenomatous hyperplasia (P=0.05) and
severe dysplasia (P=0.02). Lower expression of HAS-3 was found in severe dysplasia
compared with squamous metaplasia (P=0.01) and moderate dysplasia (P=0.01).
Epithelial Hyal-1 and −3 and HAS-1, −2, and −3 expressions were significantly higher
in pre-neoplastic lesions than in neoplastic lesions. Comparative Cox multivariate
analysis controlled by N stage and histologic tumor type showed that patients with
high HAS-3 expression in pre-neoplastic cells obtained by lung/bronchial biopsy
presented a significantly higher risk of death (HR=1.19; P=0.04). We concluded that
localization of Hyal and HAS in lung/bronchial pre-neoplastic and neoplastic lesions
was inversely related to malignancy, which implied that visualizing these factors
could be a useful diagnostic procedure for suspected lung cancer. Finalizing this
conclusion will require a wider study in a randomized and prospective trial. 相似文献
86.
87.
A. ALEEM S. AL AMOUDI S. AL‐MASHHADANI N. SIDDIQUI 《International journal of laboratory hematology》2005,27(6):395-398
Haemophagocytic syndrome (HPS) secondary to viral infections usually has a variable course and can be life‐threatening. We report a 53‐year‐old male patient who presented with fever, hepatosplenomegaly and pancytopenia. He had deranged liver function, abnormal clotting and markedly elevated serum ferritin. Bone marrow biopsy showed prominent haemophagocytosis. The patient was investigated thoroughly and found to have evidence of chronic hepatitis B‐virus (HBV) infection by serological tests and liver biopsy. Other conditions associated with HPS such as lymphoma, malignancy and other viral or bacterial infections were not present. The patient did not respond to steroids, intravenous immunoglobulins or cyclosporin but responded to etoposide and became apyrexial. He also became HBV negative on lamivudine. The patient died of infection later on but there was no evidence of recurrence of HPS. To the best of our knowledge this is the first case report of HPS associated with isolated HBV infection. 相似文献
88.
Detection of the Philadelphia chromosome in acute lymphoblastic leukemia by pulsed-field gel electrophoresis 总被引:1,自引:0,他引:1
The Philadelphia (Ph1) chromosome is an acquired abnormality in the malignant cells of 10% to 25% of patients with acute lymphoblastic leukemia (ALL). Unlike chronic myelogenous leukemia (CML), where the molecular detection of the Ph1 chromosome is relatively straightforward using conventional Southern hybridization analysis, the detection of the Ph1 chromosome in ALL is complicated by the existence of several molecular subtypes, and the fact that translocation breakpoints are dispersed over a large genomic area. To circumvent these difficulties, we investigated pulsed-field gel electrophoresis (PFGE) to determine if this method could be used directly on clinical samples to detect the Ph1 chromosome in ALL. We report that, in a study of seven patients with Ph1-positive ALL, we could easily detect the Ph1 using only a single PFGE analysis, regardless of the Ph1 subtype, and we could confirm that the translocations occur either within or very near the BCR gene in all seven. We conclude that PFGE is a useful technique for the detection of the Ph1 in ALL, which ultimately may find wide applicability in the detection of other chromosomal abnormalities in other malignancies. 相似文献
89.
Cardiac abnormalities such as mitral valve prolapse (MVP) are reported to
be common features of the Ehlers Danlos syndrome (EDS), and it has been
suggested that the majority of patients with type IV EDS will have cardiac
involvement and vascular aneurysms. However, the evidence for valve lesions
is inconsistent and often based on early clinical studies using mainly
M-mode echo. We studied 33 patients (six male, 27 female; median age 35 yr)
with EDS (30 type I, II or III, three type IV) and 30 age- and sex-matched
controls. The study assessed skin stretch and joint hypermobility using
Beighton and Contompasis scores. Echocardiographic examination included
standard two-dimensional views from the parasternal and apical windows, and
measurement of the aorta at four sites (annulus, sinotubular junction, arch
and abdominal aorta). Echocardiographic abnormalities were found in four
patients (12.1%) (one atrial septal aneurysm, one tricuspid prolapse, two
MVP) and two controls (6.7%). MVP was found in 6.1% of EDS patients and 7%
of controls. Seven patients had previously been diagnosed as having MVP;
only two were shown to have true MVP using current criteria. None of those
with type IV EDS had any echocardiographic abnormality. No patients with
EDS had mean aortic dimensions outside the normal range at any of the
points tested. Cardiac symptoms were more frequent amongst the patients
than controls (atypical chest pain 48%, P = 0.0001; palpitation 39%, P =
0.001; exertional dyspnoea 30%). A wide range of rheumatological complaints
were reported (current arthralgia 75%; recent back pain 72%, P = 0.005;
recurrent dislocation 72%). Contrary to earlier published observations, we
have not found an increased incidence of cardiac abnormalities in EDS. This
syndrome may be relatively more benign, from the cardiac point of view,
than was previously thought.
相似文献
90.
To determine the prevalence and significance of a systolic mitralmurmur heard after a first acute myocardial infarction (MI),we studied 186 consecutive patients in the coronary care unit(CCU) during a one-year period. Fifteen patients had a murmuras a result of mitral regurgitation (MR) (prevalence 8%) documentedby colour Doppler flow imaging. It was heard before the thirdday of hospitalization in 10 (67%) patients, and on the thirdday itself in the remainder. The severity of MR was graded semi-quantitatively:moderate in 12 (80%) patients, and mild, moderate to severeand severe in three respectivety. The direction of the MR jet,determined by colour flow imaging, improved the informationobtained by two-dimensional echocardiography (2D echo) thatcould only diagnose mitral leaflet abnormality in seven (47%)patients. in 10 of 15 (67%) patients, the 2D echo ejection fractionwas 40% and in eight (53%) the wall motion score obtained byanalysing 11 left ventricular (LV) segments was $$$8. Two (13%)patients died in tile CCU, four (27%) had LV failure, one anginaand eight (53%) remained asymptomaric in the hospital. Of 171patients without a systolic murmur, 22 (13%) had LV failure,13 (8%) angina and 25 (15%) died during the in-hospital stay(P-NS for these complications between patients with and withoutMR murmur). During a follow-up of 1224 months, one MRpatient died, and seven (47%) remained asymptomatic. We conclude that the prevalence of MR systolic murmurs in acuteMI patients is low. The LV function and the prognosis of a majorityof these patients is rather good. 相似文献