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11.
OHNOSHI TAISUKE; HIRAKI SHUNKICHI; KAWAHARA SHIN; YAMASHITA HIDETOSHI; YONEI TOSHIRO; ISHII JUN-ICHI; EGAWA TOMOO; KOZUKA AKIRA; HIRAKI YOSHIO; KIMURA IKURO 《Japanese journal of clinical oncology》1986,16(3):271-277
In order to assess the effectiveness of chest irradiation inaddition to intensive chemotherapy in limited stage small celllung cancer, 50 patients were randomized to receive either chemotherapyalone or chemotherapy plus chest irradiation, between April1981 and October 1985. The chemotherapy regimen consisted ofa four-drug combination of cyclophosphamide, vincristine, methotrexate,and procarbazine, and a three-drug combination of etoposide,adriamycin, and nimustine, given alternately every 8 weeks.One group of 26 patients received the chemotherapy alone, andanother group of 24 patients received chest irradiation with40 Gy between cycles 1 and 2 of the chemotherapy. Complete responserates were quite similar in the two groups; 50% for those receivingchemotherapy alone, and 59% for those receiving chemotherapyplus chest irradiation. There were no significant differencesin median survival (15 months versus 12 months) and in long-termsurvival rates between the two groups with a median follow-upperiod of 26 months. The combined modality treat ment was moretoxic than chemotherapy aIone two patients receiving such treatmentdied of radiation pneumonitis. It is concluded that chest irradiationcombined with chemotherapy does not affect the response rate,survival, or pattern of recurrence in patients with limitedstage small cell lung cancer. 相似文献
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YOSHIO HOSOBUCHI 《Pacing and clinical electrophysiology : PACE》1987,10(1):213-216
Seven patients suffering intractable pain from head and neck cancer (age 48–73, mean 57.5 years) underwent acute stimulation of dorsal periaqueductal gray matter (PAG) with immediate cessation of pain. Two patients received chronic PAG stimulation with relief of pain during stimulation. The effect was not reversed by naloxone and there were no changes in CSF peptides. 相似文献
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YOSHIO FURUKAWA M.D. Ph.D. TAKAHISA YAMADA M.D. Ph.D. TAKASHI MORITA M.D. Ph.D. YUSUKE IWASAKI M.D. MASATO KAWASAKI M.D. ATSUSHI KIKUCHI M.D. TAKASHI NAITO M.D. TADAO FUJIMOTO M.D. KENTARO OZU M.D. TAKUMI KONDO M.D. KAORUKO SENGOKU M.D. HIRONORI YAMAMOTO M.D. TOHRU MASUYAMA M.D. Ph.D. F.A.C.C. MASATAKE FUKUNAMI M.D. Ph.D. 《Journal of cardiovascular electrophysiology》2013,24(6):632-639
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Effect of glycyrrhizin on lysis of hepatocyte membranes induced by anti-liver cell membrane antibody 总被引:6,自引:0,他引:6
YASUKO SHIKI KOHJI SHIRAI YASUSHI SAITO SHO YOSHIDA YOSHIO MORI MASAFUMI WAKASHIN 《Journal of gastroenterology and hepatology》1992,7(1):12-16
Studies were made on why glycyrrhizin injection decreases the plasma aspartate aminotransferase (AST) and alanine aminotransferase activities in patients with chronic hepatitis.1 For this, rat hepatocytes were isolated, and incubated with antibody raised against rat liver cell membranes, and the effect of glycyrrhizin on their release of transaminase was investigated. Isolated rat hepatocytes released AST on incubation with anti-liver cell antibody in the presence of complement. At this time, their endogenous phospholipase A2 activity was increased. Cultured hepatocytes also released the transaminase in the presence of venom phospholipase A2. Glycyrrhizin suppressed the release of transaminase in the presence of either anti-liver cell membrane antibody or phospholipase A2. These results suggest that antibody treatment raised the phospholipase A2 activity in liver cell membranes, resulting in release of transaminases, and that glycyrrhizin suppressed this increase in phospholipase A2 activity and so inhibited the release of transaminase. 相似文献
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The Acute and Chronic Toxicities of Nivalenol in Mice 总被引:5,自引:0,他引:5
RYU JAE-CHUN; OHTSUBO KOHICHIRO; IZUMIYAMA NAOTAKA; NAKAMURA KENICHI; TANAKA TOSHITSUGU; YAMAMURA HISASHI; UENO YOSHIO 《Toxicological sciences》1988,11(1):38-47
The Acute and Chronic Toxicities of Nivalenol in Mice. Ryu,J.-C, Ohtsubo, K., Izumiy-ama, N., Nakamura, JL, Tanaka, T.,Yamamura, H., and Ueno, Y. (1988). Fundam. Appl Toxicol. 11,3847. In an attempt to ascertain precisely the toxiceffects of nivalenol (N1V), we conducted the determination ofLD50 values, and interim kills during the carcinogenic studyin mice. LD50 values (mg/kg) of NIV in 6-week-old male ddY micewere determined as 38.9 (po), 7.4 (ip), 7.2 (sc), and 7.3 (iv).Seven-week-old female C57BL/6CrSlc SPF mice were fed diets containing0, 6, 12, and 30 ppm (mg/kg) NIV over 1 year, and were assessedfor effects on body weight gain, feed efficiency, terminai organweights, hematology, and histopathology. The rates of body weightgain and feed efficiency showed a good dose-dependent correlationin all experimental periods. Gross and histopathological evaluationof the liver, thymus, spleen, kidneys, stomach, adrenal glands,pituitary gland, ovaries, sternum, bone marrow, lymph node,brain, and small intestines with or without Peyer's patch portionfrom control and all NIV-exposed mice revealed that these tissueswere normal in appearance and in histopathological structure.Also, no changes were observed in the ultrastructural studieson the bone marrow. Dietary NIV did, however, cause dose-dependentdecreases of absolute organ weights (mg) and increases of relativeorgan weights (mg/g body weight) in the terminal organ weightsrecorded. A significant leukopenia was observed in the 30 ppmgroup at 6 months and in all NIV-treated groups at 1 year. Nomarked changes were observed in the other hematological parameters.These results indicated that 6 ppm or more of dietary NIV for1 year showed a characteristic toxic effect of trichothecenemycotoxins in mice. 相似文献
18.
TAKUYA WATANABE MD AKIRA MIKAMI MD MASAMICHI MOTONISHI MD HIDEHARU HONDA MD KYOKO KYOTANI MD SHIGEHIKO URUHA MD KIYOJI TERASHIMA MD YOSHIO TESHIMA MD YOSHIRO SUGITA MD 《Psychiatry and clinical neurosciences》1998,52(2):231-232
Abstract Two cases of sleep disordered-breathing in climacteric were reported. Polysomnography including esophageal pressure (Pes) measurement was performed. Case 1 was diagnosed as upper airway resistance syndrome. Case 2 was diagnosed as obstructive sleep apnea syndrome, while many episodes of upper airway resistance also existed. Hormone replacement therapy improved clinical symptoms, and in case 1, Pes nadir was improved but incidence of arousals which was induced by breathing disturbances was not significantly changed. Sleep disordered-breathing should be suspected as a cause of sleep disorder even in females, especially in climacteric age. Pes measurement and evaluation of arousals is required. Hormone replacement therapy may release the upper airway resistance. 相似文献
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YOSHIO HIRAYASU MD HIROKAZU OHTA MD KOZO FUKAO MD CHIKARA OGURA MD JIRO MUKAWA MD 《Psychiatry and clinical neurosciences》1995,49(4):223-226
Abstract Event-related potentials (ERP) were recorded during auditory oddball tasks for a patient prior to and soon after left anterior temporal lobectomy. The N100 amplitude decreased bilaterally although the latency did not change after the lobectomy. The P300 amplitude decreased in the left hemisphere at 1 and 2 weeks after surgery, then recovered to the pre-operative level at 4 weeks. These findings suggest that the medial temporal structure participates in the generating system of P300. 相似文献