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排序方式: 共有190条查询结果,搜索用时 0 毫秒
31.
32.
33.
Detecting pre-ovulatory luteinizing hormone surges in urine 总被引:2,自引:1,他引:2
Kesner JS; Knecht EA; Krieg EF Jr; Wilcox AJ; O'Connor JF 《Human reproduction (Oxford, England)》1998,13(1):15-21
The study objectives were to determine (i) if pre-ovulatory luteinizing
hormone (LH) surges, undetected in urine by two immunoradiometric assays
(IRMA), were detectable by an ultrasensitive immunofluorometric assay
(IFMA) and (ii) the influence of creatinine adjustment on the detection and
timing of the urinary LH surges. Daily urine specimens were contributed by
healthy 25-36 year old volunteers during 14 ovulatory menstrual cycles for
an epidemiological study conducted in 1983-1985. Specimens were selected as
having been previously assayed by two IRMA without consistently detecting
LH surges. These urine specimens were remeasured using an IFMA and adjusted
for creatinine concentration. IFMA measurements revealed unambiguous LH
surges in all cycles. Adjusting IRMA urinary LH values for creatinine
concentrations revealed previously undetected LH surges in four of eight
cycles. Creatinine adjustment also altered the timing of IRMA and IFMA LH
surges by 1-5 days. These results demonstrate an IFMA that detects pre-
ovulatory LH surges in unpreserved, frozen urine from cycles where such
surges were previously undetectable. Further, creatinine adjustment can
markedly affect detection and timing of the onset and peak of the urinary
LH surge. While our analysis suggests that this adjustment improves the
validity of the LH measure, this requires further investigation.
相似文献
34.
Fugger EF; Black SH; Keyvanfar K; Schulman JD 《Human reproduction (Oxford, England)》1998,13(9):2367-2370
The world's first deliveries of normal babies after use of flow cytometric
separated human sperm cells (MicroSort) for preconception gender selection
are reported. Offspring were of the desired female gender in 92.9% of the
pregnancies. Most of these pregnancies and births were achieved after
simple intrauterine insemination.
相似文献
35.
Cooperative enhancement of F-cell formation in baboons treated with erythropoietin and hydroxyurea 总被引:2,自引:2,他引:0
Al-Khatti A; Papayannopoulou T; Knitter G; Fritsch EF; Stamatoyannopoulos G 《Blood》1988,72(2):817-819
Chronically anemic baboons on a continuous hydroxyurea regimen were treated with pulsed doses of recombinant human erythropoietin (rHuEpo) to test whether the combination of these two compounds, which individually induce F-cell production, can enhance further F-cell output. A low-F-cell-responding animal under chronic hydroxyurea treatment was given three separate pulses of Epo and responded with F- reticulocyte increments that were similar to the sum increments caused by either hydroxyurea alone or rHuEpo alone. The same results were obtained in a high-F-responding animal similarly treated. These findings suggest that rHuEpo and hydroxyurea can increase F cell numbers in an additive fashion. It is speculated that both compounds act through perturbation of erythroid differentiation kinetics. 相似文献
36.
Lack of a co-promoting effect of a 60 Hz magnetic field on skin tumorigenesis in SENCAR mice 总被引:4,自引:3,他引:1
Sasser LB; Anderson LE; Morris JE; Miller DL; Walborg EF Jr; Kavet R; Johnston DA; DiGiovanni J 《Carcinogenesis》1998,19(9):1617-1621
It has been proposed that extremely low frequency (ELF) magnetic fields may
enhance tumorigenesis through a co-promotional mechanism. This hypothesis
has been further tested using the two-stage model of mouse skin
carcinogenesis, i.e. 12-O-tetradecanoylphorbol-13-acetate (TPA)- induced
promotion of skin tumors in mice initiated by a single subcarcinogenic dose
of 7,12-dimethylbenz[a]anthracene. Experimentation described herein
utilized the SENCAR mouse and examined the effect of a magnetic field on
skin tumor promotion induced by three different doses of TPA within its
dose-response range, i.e. 0.85, 1.70 or 3.40 nmol, administered twice per
week. SENCAR mice (56/treatment group) were exposed to a 60 Hz magnetic
field having a flux density of 2 mT for 6 h/day for 5 days/week and
compared with mice exposed to the ambient magnetic field. Tumor incidence
and multiplicity were monitored weekly for 23 weeks of TPA promotion.
Statistical evaluation of the effects of the magnetic field on tumor
incidence and multiplicity did not reveal any statistically significant
effects; thus, within the sensitivity limits imposed by the animal model
and the exposure parameters employed, no promotional or co-promotional
effect of a 2 mT magnetic field on skin tumor development in SENCAR mice
could be demonstrated.
相似文献
37.
Increased colonic wall thickness has been reported in patients exposed to large doses of high strength pancreatic enzyme preparations who did not develop fibrosing colonopathy. This has been interpreted as evidence for a spectrum of subclinical disease. The relation between sonographically measured colonic wall thickness and pancreatic enzyme preparation and dose was studied in 86 children with cystic fibrosis (CF). Colonic wall thickness of a control group was also measured. The average thickness in all colonic regions was higher in the CF group (overall average range 0.7-2.5 mm v 0.6-1.4 mm in the control group). There was no significant relation between colonic wall thickness and age, sex, total dose of lipase, or copolymer. Apart from one patient with an early colonic stricture, none of those exposed to high doses of lipase, or the methacrylic acid copolymer Eudragit L30 D55, showed evidence of subclinical damage to the colon. The reproducibility of the sonographic measurements was poor. 相似文献
38.
39.
van der Put NM; van der Molen EF; Kluijtmans LA; Heil SG; Trijbels JM; Eskes TK; Van Oppenraaij-Emmerzaal D; Banerjee R; Blom HJ 《QJM : monthly journal of the Association of Physicians》1997,90(8):511-517
Elevated homocysteine (Hcy) levels are observed in two apparently unrelated
diseases: neural-tube defects (NTD) and premature vascular disease.
Defective human methionine synthase (MS) could result in elevated Hcy
levels. We sequenced the coding region of MS in 8 hyperhomocysteinaemic
patients (4 NTD patients and 4 patients with pregnancies complicated by
spiral arterial disease, SAD). We identified only one mutation resulting in
an amino acid substitution: an A-->G transition at bp 2756, converting
an aspartic acid (D919) into a glycine (G). We screened genomic DNA for the
presence of this mutation in 56 NTD patients, 69 mothers of children with
NTD, 108 SAD patients and 364 controls. There was no increased prevalence
of the GG and AG genotypes in NTD patients, their mothers or SAD patients.
The D919G mutation does not seem to be a risk factor for NTD or vascular
disease. We then examined the mean Hcy levels for each MS genotype. There
was no correlation between GG- or AG-genotype and Hcy levels. The D919G
mutation is thus a fairly prevalent, and probably benign polymorphism. This
study, though limited, provides no evidence for a major involvement of MS
in the aetiology of homocysteine-related diseases such as NTD or vascular
disease.
相似文献
40.
Distinct ongoing Ig heavy chain rearrangement processes in childhood B- precursor acute lymphoblastic leukemia 总被引:2,自引:3,他引:2
Steenbergen EJ; Verhagen OJ; van Leeuwen EF; von dem Borne AE; van der Schoot CE 《Blood》1993,82(2):581-589
Acute lymphoblastic leukemia (ALL) is thought to arise from the clonal expansion of a single transformed precursor cell. However, an oligoclonal Ig heavy chain (IgH) rearrangement pattern has been observed in 30% of ALL patients and was shown to be the result of ongoing rearrangement events. The extent and nature of these ongoing rearrangement processes in individual patients has so far remained obscure. We performed a detailed analysis of leukemic VHDJH rearrangements in three children with B-precursor ALL at diagnosis and one B-lymphoid blast crisis of a child with Ph+ chronic myeloid leukemia at diagnosis and relapse. The children were selected because they presented with multiple IgH rearrangements on Southern blot analysis. Polymerase chain reaction analysis of leukemic cells from two B-precursor ALL patients showed exclusively two groups of related sequences resulting from VH gene replacement events. Most VH gene replacements involved 3' located acceptor VH genes. Analysis of cells from the other B-precursor ALL patient showed exclusively related sequences as a result of VH gene joinings to a pre-existing DJH rearrangement. In the B-lymphoid blast crisis, a single germline precursor cell had generated multiple unrelated rearrangements and additional groups of related rearrangements resulting from VH to DJH joinings. Direct proof for the VH to DJH joining mechanism was obtained by amplification of the expected preexisting DJH rearrangements. Our findings suggest that the pattern of ongoing rearrangements in an individual patient reflects the IgH rearrangement status of the precursor cell at the time of malignant transformation. Sequence analysis of VHDJH rearrangements at diagnosis may therefore allow a prediction of the reliability of complementarity determining region 3 probes for the detection of minimal residual disease. 相似文献