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31.
P. Copin L. Pesquer P. Meyer M.-H. Moreau Durieux V. Hummel J. Manelfe E. Desportes S. Djebbar A. Larbi D. Toledano E. Schouman-Claeys B. Dallaudière 《Journal de Traumatologie du Sport》2014
We present the case of a professional volleyball player, referred for posteromedial knee pain following a competition. MRI diagnosed an anterior arm of the semi-membraneous tendinitis associated with a semimembranosus–tibial collateral ligament bursitis. Some key points of the anatomy of the distal semimembranosus complex must be identified; five tendinous arms (including the anterior, or tibial arm) are to be seen with regard to the two synovial bursae associated. Indeed, a fluid distension of the semimembranosus–tibial collateral ligament, recently described, must be considered as a sentinel lesion and could turn the radiologist toward an injury of the distal semimembranosus complex. The physiopathological mechanism of the injury of the distal semimembranosus complex distinguishes two kinds of lesion: the tendinous overstressing and the hyperextension of the young and athletic subject will be responsible respectively for isolated tendinitis of the direct and reflected tendons. The tendinosis of the middle-aged subject will be secondary in repeated microtraumas. 相似文献
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Nadjib Hammoudi Dimitri Arangalage Morad Djebbar Katia Stankovic Stojanovic Magali Charbonnier Richard Isnard Robert Girot Pierre-Louis Michel François Lionnet 《The international journal of cardiovascular imaging》2014,30(7):1297-1304
Chronic volume overload in sickle-cell anemia (SCA) is associated with left ventricular (LV) enlargement and hypertrophy. The effect of the disease on LV systolic function remains debated. The aim of our study was to investigate LV systolic function in SCA patients using 2D speckle-tracking imaging. We compared 30 steady state asymptomatic adult SCA patients (17 women, mean age 24.7 ± 5.1 years) with 30 age and sex-matched healthy subjects (17 women, mean age 25.0 ± 4.9 years). In addition to conventional echocardiographic parameters including LV ejection fraction (LVEF) and LV mass index (LVMi), global longitudinal strain (GLS) and strain rate (GLSR) were measured. GLS (?17.9 ± 2.0 vs. ?19.7 ± 2.5 %, p = 0.004) and GLSR (?0.92 ± 0.09 vs. ?1.07 ± 0.17 s?1, p < 0.0001) values were lower in SCA patients while LVEF values (60.1 ± 3.8 vs. 61.7 ± 4.7 %, p = 0.30) were not different. LVMi was increased in SCA patients (100.7 ± 23.5 vs. 72.4 ± 15.2 g/m2, p = 0.0001) and GLSR was significantly lower in the subgroup of patients with LV hypertrophy (?0.88 ± 0.09 vs. ?0.96 ± 0.08 s?1, p = 0.02). In SCA patients LVMi was correlated to GLS (r = 0.58, p = 0.001) and GLSR (r = 0.45, p = 0.015) pleading in favor of a pathological LV remodeling. Asymptomatic SCA patients exhibited a subclinical alteration of LV systolic function. Myocardial dysfunction appears to be linked to the degree of LV hypertrophy. 2D speckle-tracking imaging might be useful for long-term follow-up and to study the natural course of LV dysfunction in SCA patients. 相似文献
34.
S. R. Khan F. Atmani P. Glenton Z.-C. Hou D. R. Talham M. Khurshid 《Calcified tissue international》1996,59(5):357-365
The ultrastructure of the organic matrix of demineralized urinary stones was examined by standard transmission and scanning
electron microscopy as well as after malachite green-glutaraldehyde fixation. Crystal ghosts of both calcium oxalate and calcium
phosphate were made of amorphous material and were dispersed in a matrix containing amorphous, fibrillar, and membranous substances.
Malachite green positive material was seen to be associated with the ghosts, as well as with the membranous and fibrillar
components of the organic matrix. Calcium oxalate and calcium-phosphate crystals, induced in human urine in vitro were also
found to be associated with an organic matrix containing lipids and proteins. It is suggested that the intimate association
between crystals and lipids is a result of the involvement of cellular membranes in the nucleation of these crystals.
Received: 28 August 1995 / Accepted: 22 December 1995 相似文献
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Aim of the study
The aim of the present study is to evaluate the diuretic potential and effect on urinary electrolytes of aqueous Erica multiflora L. (Ericaceae) flowers and Cynodon dactylon L. (Poaceae) rhizomes extracts in rats.Materials and methods
Different concentrations of these plants extract (0.125, 0.250, and 0.500 g/kg of body weight) or the reference drug furosemide (0.015 g/kg) were administrated orally to hydrated male Wistar rats and their urine output was measured at several interval of time after a single dose administration. Furthermore, a toxicological effect of both plants was undertaken as well.Results
The results showed that furosemide induced significant diuresis and electrolytes excretion during the first hours. Plant extracts increased significantly urinary output and electrolytes excretion at the dose of 0.250 g/kg for Erica multiflora and 0.500 g/kg for Cynodon dactylon. This diuretic effect seems to be not related to K+ plant content. Urinary pH remained mostly unchanged during the course of the study for both plant extracts. No lethality was observed among animals when using Erica multiflora even at the dose of 10 g/kg while Cynodon dactylon, instead, caused 50% of rat death (LD50) at 4.5 g/kg.Conclusion
We concluded that both aqueous herb extracts administered, particularly, at the dose of 0.500 g/kg induce significant effect on urinary output of water and electrolytes and justify their use as diuretic remedy in traditional medicine. 相似文献37.
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Aissaoui Y Belyamani L El Wali A Idrissi Hajjouji SM Atmani M Drissi Kamili N 《Annales fran?aises d'anesthèsie et de rèanimation》2006,25(10):1041-1045
OBJECTIVE: To investigate the influence of pretreatment with a low dose of etomidate (priming dose) on the incidence of etomidate-induced myoclonus. STUDY DESIGN: Prospective randomized double-blind study. METHODS: Forty six patients ASA physical status I - II, scheduled for abdominal elective surgery, were allocated randomly to receive either pre-treatment 0.03 mg/kg of etomidate (priming group) or placebo (control group). Sixty-seconds after the pre-treatment was injected, anesthesia was induced with etomidate 0.3 mg/kg and 60 seconds later induction was completed with fentanyl (3 microg/kg) and vecuronium (0.1 mg/kg). The occurrence and intensity of myoclonus were graded clinically by a blinded observer as: 0=no myoclonus, 1=mild myoclonus, 2=moderate myoclonus and 3=severe myoclonus. Statistical analysis: Fisher test exact for qualitative variable and Student t-test for quantitative variables. RESULTS: Demographic data and the average dose of etomidate used during the induction were similar in the 2 groups (0.29+/-0.032 mg/kg in the priming group and 0.30+/-0.029 mg/kg in the control group). Twenty patients (87%) in the control group experienced myoclonic movements whereas only 6 patients (26%) in the control group had such movements (P<0,001). CONCLUSION: Pretreatment with etomidate (0.03 mg/kg), given 60 seconds before induction of anesthesia, is effective at reducing etomidate-induced myoclonus, without related side-effect. 相似文献
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Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test 下载免费PDF全文
J. Thevenon Y. Duffourd A. Masurel‐Paulet M. Lefebvre F. Feillet S. El Chehadeh‐Djebbar J. St‐Onge A. Steinmetz F. Huet M. Chouchane V. Darmency‐Stamboul P. Callier C. Thauvin‐Robinet L. Faivre J.B. Rivière 《Clinical genetics》2016,89(6):700-707
The current standard of care for diagnosis of severe intellectual disability (ID) and epileptic encephalopathy (EE) results in a diagnostic yield of ~50%. Affected individuals nonetheless undergo multiple clinical evaluations and low‐yield laboratory tests often referred to as a ‘diagnostic odyssey’. This study was aimed at assessing the utility of clinical whole‐exome sequencing (WES) in individuals with undiagnosed and severe forms of ID and EE, and the feasibility of its implementation in routine practice by a small regional genetic center. We performed WES in a cohort of 43 unrelated individuals with undiagnosed ID and/or EE. All individuals had undergone multiple clinical evaluations and diagnostic tests over the years, with no definitive diagnosis. Sequencing data analysis and interpretation were carried out at the local molecular genetics laboratory. The diagnostic rate of WES reached 32.5% (14 out of 43 individuals). Genetic diagnosis had a direct impact on clinical management in four families, including a prenatal diagnostic test in one family. Our data emphasize the clinical utility and feasibility of WES in individuals with undiagnosed forms of ID and EE and highlight the necessity of close collaborations between ordering physicians, molecular geneticists, bioinformaticians and researchers for accurate data interpretation. 相似文献