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991.
Phase II Study to Evaluate the Efficacy and Safety of Rilotumumab and Bevacizumab in Subjects with Recurrent Malignant Glioma 下载免费PDF全文
992.
993.
Mucinous tubular and spindle cell carcinoma: a report of 15 cases and a review of the literature 总被引:10,自引:0,他引:10
Ferlicot S Allory Y Compérat E Mege-Lechevalier F Dimet S Sibony M Couturier J Vieillefond A 《Virchows Archiv : an international journal of pathology》2005,447(6):978-983
Mucinous tubular and spindle cell carcinomas are low-grade renal epithelial neoplasms, which were first recognized as a specific
entity in the World Health Organization 2004 classification. Forty-five documented cases have been reported. We present 15
additional cases that were incidentally discovered in ten women and five men, with a mean age of 53 years. The tumor is characteristically
made up of large eosinophilic regular spindle cells separated by a myxoid stroma with intercellular alcian-blue-positive clear
droplets. In peripheral areas, elongated tubules and papillae covered by cubic cells are found. Until this entity had been
defined, pathologists used to classify these tumors as variants of solid papillary carcinomas with compressed and elongated
papillae, metanephric adenomas, and sarcomatoid carcinomas. In the literature, cytogenetic data indicate various chromosomal
losses and gains, but no loss of 3p or trisomy 7 and/or trisomy 17. In two cases, we demonstrate chromosomal loss involving
chromosomes 1, 4, 6, 11, 8, 13, 14, 15, 18, and 22. In our 15 cases, immunohistochemistry favored a distal tubule origin (EMA+, AE1/AE3+, CK7+, CK19+, E-cadherin+, AMACR+, and CD10−). Prognosis was favorable in our cases, while in the literature, two metastatic cases were reported. Further investigations
are required to determine the frequency and true prognosis of these tumors, which are easily identifiable morphologically. 相似文献
994.
Resynchronization of hormonal rhythms after an eastbound flight in humans: effects of slow-release caffeine and melatonin 总被引:2,自引:0,他引:2
Piérard C Beaumont M Enslen M Chauffard F Tan DX Reiter RJ Fontan A French J Coste O Lagarde D 《European journal of applied physiology》2001,85(1-2):144-150
The aim of this work was to investigate the potential chronobiotic properties of slow-release caffeine, in comparison with
melatonin, on resynchronization of endogenous melatonin and cortisol secretions after an eastbound flight by jet incurring
a time loss of 7 h. A group of 27 reservists of the US Air Force received either slow-release caffeine (300 mg), melatonin
(5 mg) or placebo before, during and/or after the transmeridian flight. Saliva and urine were sampled before the flight in
the United States (from day –2 to day 0) and after the flight in France (from day 1 to day 10). Saliva was collected once
a day on waking to determine saliva melatonin and cortisol concentrations. In addition, concentrations of caffeine in saliva
were determined three times a day and of 6-sulphatoxymelatonin in urine collected overnight to check that the treatment regimes
had been complied with. From day 3 to day 5, post-flight saliva melatonin concentrations were significantly different from
control values in the placebo group only. During treatment with melatonin, the mean urinary 6-sulphatoxymelatonin concentration
in the melatonin group was more than twice as high as in the two other groups. In the slow-release caffeine group and the
melatonin group, mean saliva cortisol concentrations were significantly lower than control from day 2 to day 5, whereas the
placebo group had a mean saliva cortisol concentration significantly lower than the control value from day 2 to day 9. In
conclusion, these results indicate that administration of slow-release caffeine, as well as of melatonin, allows a faster
resynchronization of hormone rhythms during the 4 days following an eastbound flight incurring the loss of 7 h.
Electronic Publication 相似文献
995.
Jocelyn Dupuis Annick Prfontaine Louis Villeneuve Nathalie Ruel Frdric Lefebvre Angelino Calderone 《Cardiovascular pathology》2007,16(6):321-328
BACKGROUND: Congestive heart failure (CHF) causes structural modifications of the lungs that contribute to the functional limitations of affected subjects. We hypothesized that bone marrow-derived progenitor cells could contribute to lung structural remodelling after myocardial infarction (MI). METHODS: Wistar rats were irradiated and received a bone marrow transplant (BMT) from green fluorescent protein (GFP) transgenic rats, followed 5 weeks later by coronary artery ligation or sham operation. Five weeks after MI, lung immunofluorescence studies were performed and GFP expression evaluated by Western immunoblotting. RESULTS: After MI, rats developed lung structural remodelling characterized by myofibroblast (MF) proliferation in the alveolar septa. After BMT, some GFP+ cells were found in the lungs of sham animals. The amount of GFP+ cells in the lungs of MI rats was greatly increased with evidence of differentiation into MFs, as evaluated by co-localization correlation analysis with smooth muscle alpha-actin (P<.01). These cells were particularly abundant in the perivenular regions where they incorporated into the wall of blood vessels. There was a threefold increase in lung GFP protein expression after MI (P=.01). CONCLUSIONS: After MI, bone marrow-derived progenitor differentiates into lung MFs. This novel pathophysiologic process may contribute to the pulmonary manifestations of CHF and could have significant therapeutic implications. 相似文献
996.
Xhonneux Annick Langhendries Jean-Paul Martin Françoise Seidel Laurence Albert Adelin Dain Elena Totzauer Martina Grote Veit Luque Veronica Closa-Monasterolo Ricardo Dionigi Alice Re Verduci Elvira Gruszfeld Darius Socha Piotr Koletzko Berthold 《Maternal and child health journal》2022,26(6):1274-1282
Maternal and Child Health Journal - Maternal perception of child weight status in children with overweight or obesity has received a lot of attention but data on paternal perception of children... 相似文献
997.
998.
Isabelle Bailleul-Forestier Veroniek Verhaeghe Jean-Pierre Fryns Frans Vinckier Dominique Declerck Annick Vogels 《International journal of paediatric dentistry / the British Paedodontic Society [and] the International Association of Dentistry for Children》2008,18(1):40-47
BACKGROUND: Prader-Willi syndrome (PWS) is a rare disorder caused by genetic defects in certain regions of chromosome 15q11-13. It is characterized by severe neonatal hypotonia and feeding problems, childhood-onset hyperphagia and obesity, short stature, facial dysmorphy, hypogonadism, learning and behavioural difficulties, and dental abnormalities. AIM: To describe the oro-dental phenotypic spectrum of patients with PWS. DESIGN: Fifteen PWS patients (3-35 years of age) being followed at the Centre for Human Genetics of the University Hospital of Leuven were examined at the dental clinic of the same institution. Medical information collected included age at diagnosis, body mass index (BMI) and level of cognitive functioning. Oral, clinical and radiological evaluations were performed. Caries experience (cavitation level), dental erosion and salivary flow rates were assessed. RESULTS: The 15 patients had dmft/DMFT scores ranging from 0 to 28, while nine were cavity-free. Those with severe caries experience also presented advanced dental erosion. BMI ranged from 16 to 42.6. There was no association between BMI and caries experience or erosive tooth wear. The PWS patients in our survey presented with a more favourable oral health status than those in previous studies. This might be due to early diet management or better oral hygiene during childhood or both. 相似文献
999.
Invasive aspergillosis is extremely rare in immunocompetent children. Here we describe the clinical, radiologic, and laboratory course of fatal invasive pulmonary and central nervous system aspergillosis in a previously healthy child after a near-drowning incident with submersion in a pond. Findings were compared with data from the literature, which is reviewed. Serum Aspergillus galactomannan levels were determined retrospectively and were compared with the results of routine microbiological and radiologic examinations, showing a significant diagnostic and therapeutic delay of the routine diagnostic approach in comparison with the use of the Aspergillus galactomannan assay. This delay may have contributed to the fatal course. Serial determination of serum Aspergillus galactomannan may be helpful in diagnosing invasive aspergillosis early in case of pulmonary disease after near-drowning and may contribute to an early appropriate treatment. Currently voriconazole, eventually in combination with caspofungin, should be considered as the drug of choice in the management of invasive aspergillosis after near-drowning. 相似文献
1000.
Michael J. Paldino MD Daniel Barboriak MD Annick Desjardins MD Henry S. Friedman MD James J. Vredenburgh MD 《Journal of magnetic resonance imaging : JMRI》2009,29(5):1199-1205