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991.
Reading epilepsy is a rare form of reflex epilepsy that occurs exclusively during reading. In this report, we describe a patient in whom seizure was the initial symptom of idiopathic hypoparathyroidism. A 31-year-old man experienced seizures three times in different bookshops while browsing. Chvostek's sign was observed. Serum calcium and parathyroid hormone levels were decreased. Brain computed tomography revealed symmetrical calcification at the dentate nuclei of the cerebellum and the basal ganglia. The interictal electroencephalography was normal. There was no photoparoxysmal response. After amelioration of serum calcium level with oral administration of vitamin D, seizure attacks ceased without antiepileptic drugs. This case is, to our knowledge, the first report of reading epilepsy associated with hypocalcemia due to idiopathic hypoparathyroidism. The psychological stress of reading at bookshops without buying might have triggered seizures under CNS hyperexcitability due to hypocalcemia. 相似文献
992.
Ikeda K Ito H Hidaka T Takazawa T Sekine T Yoshii Y Hirayama T Kawabe K Kano O Iwasaki Y 《Internal medicine (Tokyo, Japan)》2011,50(9):1061-1064
A 51-year-old woman had developed fever and consciousness disturbance at 47 years of age. Brain magnetic resonance imaging (MRI) revealed acute disseminating encephalomyelitis (ADEM)-like lesions without gadolinium enhancement (GDE). One year later, she had an episode of bilateral optic neuritis and cerebellar ataxia. Speech deficit and right hand weakness occurred at the age of 51 years. Neurological examination showed motor aphasia, finger agnosia, right-left disorientation, and right hand paresis. Neuromyelitis optica (NMO)-IgG was seropositive. Cerebrospinal fluid examination showed negative results for myelin basic protein and oligoclonal IgG band. The IgG index was normal. Brain MRI revealed a tumefactive lesion in the left temporo-parietal region and conglomerate ovoid lesions in the pericallosal regions. No GDE was found in the brain lesions. Visual evoked potential test showed bilateral prolongation of P100 latencies. She was treated twice with methylprednisolone pulse therapy followed by oral prednisolone, but the motor aphasia did not respond to steroid treatment. She had no prior history of myelitis and was diagnosed as NMO spectrum disorder (NMOSD). Similar to previous studies of NMO-IgG seropositive extensive brain lesions, this patient with NMOSD indicated no GDE in tumefactive lesions at two episodes of encephalopathy. Compared to multiple sclerosis (MS), a high frequency of non-enhancing tumefactive lesions is reported in patients with NMO or NMOSD. The absence of GDE in tumefactive lesions could help to differentiate between NMO and MS. 相似文献
993.
994.
Suzuki H Saitoh Y Koh E Hoshino H Kase D Kasei Y Azuhata Y Kishi H Hiroshima K Sekine Y 《Surgery today》2011,41(2):258-261
Pulmonary sclerosing hemangioma is relatively rare and is usually considered a benign tumor. There have been no reports of
pulmonary sclerosing hemangioma with pleural dissemination. This report presents an extremely rare case of pulmonary sclerosing
hemangioma with pulmonary dissemination. A 57-year-old woman was found to have an abnormal shadow in the right lower lung
field on chest X-ray. Chest computed tomography (CT) indicated a 2.5-cm mass in the right lower lobe. A bronchoscopic biopsy
failed to identify malignant cells, which led to the patient undergoing an excisional lung biopsy. Intraoperative findings
showed a tumor in the right lower lobe with multiple small nodules in the pleura. The pathological findings revealed that
the tumor was sclerosing hemangioma with pleural dissemination. Annual follow-up CT showed irregular pleural thickness, which
suggested progressive dissemination 3 years after the operation. Although pulmonary sclerosing hemangioma is regarded as a
benign tumor, the potential for malignancy may be a consideration in this setting. 相似文献
995.
996.
997.
Okada M Okabe A Uchihori Y Kitamura H Sekine E Ebisawa S Suzuki M Okayasu R 《British journal of cancer》2007,96(11):1707-1710
To investigate the long-term biological effect of extreme low dose ionising radiation, we irradiated normal human fibroblasts (HFLIII) with carbon ions (290 MeV u(-1), 70 keV microm(-1)) and gamma-rays at 1 mGy (total dose) once at a low dose rate (1 mGy 6-8 h(-1)), and observed the cell growth kinetics up to 5 months by continuous culturing. The growth of carbon-irradiated cells started to slow down considerably sooner than that of non-irradiated cells before reaching senescence. In contrast, cells irradiated with gamma-rays under similar conditions did not show significant deviation from the non-irradiated cells. A DNA double strand break (DSB) marker, gamma-H2AX foci, and a DSB repair marker, phosphorylated DNA-PKcs foci, increased in number when non-irradiated cells reached several passages before senescence. A single low dose/low dose rate carbon ion exposure further raised the numbers of these markers. Furthermore, the numbers of foci for these two markers were significantly reduced after the cells became fully senescent. Our results indicate that high linear energy transfer (LET) radiation (carbon ions) causes different effects than low LET radiation (gamma-rays) even at very low doses and that a single low dose of heavy ion irradiation can affect the stability of the genome many generations after irradiation. 相似文献
998.
Saito H Takahashi S Nagata M Tsuchiya T Mugishima H Yan K Kondo Y Matsuyama T Sekine T Igarashi T 《Pediatric nephrology (Berlin, Germany)》2009,24(3):609-612
Recently, disorders of the slit diaphragm have been considered as major causes of proteinuria in renal disease and the charge
barrier function of the glomerular capillary wall has been given less attention. We evaluated the charge selectivity index
(CSI) in 40 patients with podocyte disease (PD), 75 with chronic glomerulonephritis (CGN), and 8 with Dent disease, to reexamine
the charge barrier function. We evaluated CSI in Dent disease because the urinary protein profile in Dent disease was assumed
to be a concentrate of a normal glomerular filtrate. CSI was defined as the renal clearance ratio between IgA and IgG. CSI
values (mean ± SD) in the CGN and PD groups and in Dent disease were 1.12 ± 0.25, 0.42 ± 0.31, and 0.16 ± 0.06, respectively,
suggesting that the charge barrier function was defective in the CGN group and of reduced capacity in the PD group. The results
suggest that functional interactions between the slit diaphragm and the glomerular basement membrane exist, and that a slit
diaphragm disorder is accompanied by a decrease in the charge barrier function in PD, as argued by the conventional hypothesis. 相似文献
999.
Okada K Hashimoto K Iwata Y Nakamura K Tsujii M Tsuchiya KJ Sekine Y Suda S Suzuki K Sugihara G Matsuzaki H Sugiyama T Kawai M Minabe Y Takei N Mori N 《Progress in neuro-psychopharmacology & biological psychiatry》2007,31(1):187-190
BACKGROUND: The neurobiological basis for autism remains poorly understood. Given the key role of transforming growth factor-beta1 (TGF-beta1) in brain development, we hypothesized that TGF-beta1 plays a role in the pathophysiology of autism. In this study, we studied whether serum levels of TGF-beta1 are altered in patients with autism. METHODS: We measured serum levels of TGF-beta1 in 19 male adult patients with autism and 21 age-matched male healthy subjects using enzyme-linked immunosorbent assay (ELISA). RESULTS: The serum levels (7.34+/-5.21 ng/mL (mean+/-S.D.)) of TGF-beta1 in the patients with autism were significantly (z=-5.106, p<0.001) lower than those (14.48+/-1.64 ng/mL (mean+/-S.D.)) of normal controls. However, there were no marked or significant correlations between serum TGF-beta1 levels and other clinical variables, including Autism Diagnostic Interview-Revised (ADI-R) scores, Yale-Brown Obsessive-Compulsive Scale (Y-BOCS), aggression, Theory of Mind, and Intellectual Quotient (IQ) in patients. CONCLUSIONS: These findings suggest that decreased levels of TGF-beta1 may be implicated in the pathophysiology of autism. 相似文献
1000.