全文获取类型
收费全文 | 286篇 |
免费 | 11篇 |
专业分类
儿科学 | 19篇 |
妇产科学 | 5篇 |
基础医学 | 25篇 |
口腔科学 | 9篇 |
临床医学 | 13篇 |
内科学 | 90篇 |
皮肤病学 | 12篇 |
神经病学 | 18篇 |
特种医学 | 1篇 |
外科学 | 63篇 |
综合类 | 2篇 |
预防医学 | 3篇 |
眼科学 | 2篇 |
药学 | 12篇 |
肿瘤学 | 23篇 |
出版年
2022年 | 2篇 |
2021年 | 2篇 |
2017年 | 1篇 |
2016年 | 2篇 |
2015年 | 8篇 |
2014年 | 8篇 |
2013年 | 4篇 |
2012年 | 4篇 |
2011年 | 3篇 |
2010年 | 11篇 |
2009年 | 5篇 |
2008年 | 2篇 |
2007年 | 2篇 |
2006年 | 21篇 |
2005年 | 9篇 |
2004年 | 11篇 |
2003年 | 8篇 |
2002年 | 9篇 |
2001年 | 1篇 |
2000年 | 3篇 |
1999年 | 4篇 |
1998年 | 17篇 |
1997年 | 19篇 |
1996年 | 14篇 |
1995年 | 18篇 |
1994年 | 7篇 |
1993年 | 15篇 |
1992年 | 6篇 |
1991年 | 7篇 |
1990年 | 6篇 |
1989年 | 4篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 8篇 |
1985年 | 3篇 |
1984年 | 2篇 |
1983年 | 3篇 |
1982年 | 1篇 |
1981年 | 3篇 |
1980年 | 5篇 |
1979年 | 1篇 |
1978年 | 2篇 |
1975年 | 1篇 |
1970年 | 1篇 |
1959年 | 3篇 |
1958年 | 7篇 |
1957年 | 6篇 |
1956年 | 4篇 |
1955年 | 1篇 |
1954年 | 7篇 |
排序方式: 共有297条查询结果,搜索用时 171 毫秒
21.
Jaundice and Renal Failure Following Radical Surgery for Cancer: An Analysis of Five Autopsied Cases
HATTORI NOBU; NAKAMOTO YASUSHI; KOBAYASHI KENICHI; IIZUKA TOSHIFUMI; MATSUMOTO KEIICHI 《Japanese journal of clinical oncology》1980,10(1):21-29
An analysis of postoperative jaundice and renal failure in fiveautopsied cases is presented. Two patients had total resectionof esophageal cancer, one had a subtotal gastrectomy, and theother two had radical operations for urinary bladder carcinoma.Halothane was used for anesthesia for three patients, and allfive required blood transfusions. Postoperatively, jaundiceand azotemia developed between the 1st and 7th days, with deathsix to 10 days after surgery. Total bilirubin ranged from 1.5to 13.4mg/dl despite the normal or modest rise in hepatic enzymes.BUN varied from 46 to 288 mg/dl. Pre- and postoperative ECGrevealed a prolongation of QTc in all cases. At autopsy, theliver, kidneys and heart showed a definite increase in weight.The salient hepatic pathology included diffusely dilated spaceof Disse, centrilobular bile stasis and steatosis. This, alongwith acute tubular necrosis confirmed at autopsy, was thoughtto be due to ischemia. Although the significance of prolongedQTc remains uncertain, it is worthy of attention as one of thepreoperative checks. 相似文献
22.
23.
TADAO HASEGAWA AKIRA OKAMOTO TAKUYA KAMIMURA ICHIRO TATSUNO SHIN‐NOSUKE HASHIKAWA MITSUTAKA YABUTANI MASAKADO MATSUMOTO KEIKO YAMADA MASANORI ISAKA MASAAKI MINAMI MICHIO OHTA 《APMIS : acta pathologica, microbiologica, et immunologica Scandinavica》2010,118(3):167-178
Hasegawa T, Okamoto A, Kamimura T, Tatsuno I, Hashikawa S‐N, Yabutani M, Matsumoto M, Yamada K, Isaka M, Minami M, Ohta M. Detection of invasive protein profile of Streptococcus pyogenes M1 isolates from pharyngitis patients. APMIS 2010; 118: 167–78. Streptococcal toxic shock syndrome (STSS) is a re‐emerging infectious disease in Japan and many other developed countries. Epidemiological studies have revealed that the M1 serotype of Streptococcus pyogenes is the most dominant causative isolate of STSS. Recent characterization of M1 isolates revealed that the mutation of covS, one of the two‐component regulatory systems, plays an important role in STSS by altering protein expression. We analyzed the M1 S. pyogenes clinical isolates before or after 1990 in Japan, using two‐dimensional gel electrophoresis (2‐DE) and pulsed‐field gel electrophoresis (PFGE). PFGE profiles were different between the isolates before and after 1990. Markedly different profiles among isolates after 1990 from STSS and pharyngitis patients were detected. Sequence analysis of two‐component regulatory systems showed that covS mutations were detected not only in STSS but also in three pharyngitis isolates, in which proteins from the culture supernatant displayed the invasive type. The mutated CovS detected in the pharyngitis isolates had impaired function on the production of streptococcal pyrogenic exotoxin B (SpeB) analyzed by 2‐DE. These results suggest that several covS mutations that lead to the malfunction of the CovS protein occurred even in pharyngeal infection. 相似文献
24.
25.
KAKIZOE TADAO; OHTANI MIKINOBU; TOBISU KENICHI; MATSUMOTO KEIICHI; TESHIMA SHINICHI; KISHI KIYOZO 《Japanese journal of clinical oncology》1986,16(1):59-63
A primary neoplasm arising in a vesical diverticulum was cystectomizedand analyzed by step-sectioning of the whole bladder in an attemptto determine the carcinogenic process. Serial sections of thecystectomy specimen revealed a small area of mild dysplasiain the mucosa of the bladder and the diverticulum without atumor. Most of the mucosal cells in the tumor-bearing diverticulumwere desquamated, but a small area of dysplasia in the remainingcells was also observed. 相似文献
26.
Mitsuru MIZUNO Mitsuo IIDA Takayuki MATSUMOTO Shigeo INOUE Kazunori HOSHIKA Michio SHIMIZU Tsukasa TSUNODA 《Digestive endoscopy》1999,11(1):47-51
Abstract: A 59-year-old male with an established diagnosis of malignant melanoma of the nasal cavity plus multiple pulmonary metastases was referred to our hospital because of abdominal pain and vomiting. Double-contrast study of the small intestine revealed a filling defect in the middle of the ileum. lntraoperative enteroscopy revealed that the ileal tumor was ulcerated, and that it was covered by ileal mucosa of normal appearance. Because no other lesions were identified within the intestine, the ileal segment with the tumor was surgically removed. The tumor was diagnosed as malignant melanoma with a histology similar to that of nasal mass. The patient has survived for the subsequent 13 months, during which no gastrointestinal symptoms recurred. Our case suggests that metastasis should be included in the differential diagnosis of a single small intestinal tumor. (Dig Endose 1999; 11: 47–51) 相似文献
27.
M. YOSHIMOTO E. KINOSHITA T. BABA T. MATSUMOTO N. NI-KAWA I. MATSUDA Y. TSUJI 《Acta paediatrica (Oslo, Norway : 1992)》1990,79(12):1247-1251
ABSTRACT. An extreme dwarf 10-year-old boy was described. His clinical features resemble those of isolated GH deficiency type 1A, but the Southern blot analysis showed no gross deletion in the GH structural gene. Endocrinological evaluations showed severe GH and PRL deficiencies, and mild TSH deficiency. The simultaneous deficiencies of anterior pituitary hormones in our patient resemble those of the Snell and Ames dwarf mice and suggest a common etiology. The evolutionary and embryological similarities between GH and PRL imply that mutations at a gene which controls GH and PRL production in somatotropes and lactotropes or at a gene of which product affects the embryological development from a common ancestral cell in the anterior pituitary gland may be a primary defect in our patient. 相似文献
28.
29.
Tetsu ENDO Hirohiko SATO Junichi KOEDA Osamu TAKAHASHI Yohichi HAGA Toshinobu SATOH Yoichi CHIBA Kazuhito MATSUMOTO Akihiro MUNAKATA 《Digestive endoscopy》1999,11(3):255-258
A 19–year-old woman visited our hospital complaining of fever and epigastral-gia. Upper gastrointestinal endoscopy showed minute discrete erosions surrounded by elevated mucosa about one millimeter in diameter in the esophagus and aphthoid erosions in the stomach. Biopsy samples obtained from the esophagus showed non-caseating epitheloid granulomas, suggesting Crohn's disease. Colonoscopy showed a small erosion in the cecum adjacent to the vermiform appendix and biopsy showed non-caseating epitheloid granulomas and Crohn's disease was diagnosed. In hospital, she was treated with elemental diet and 5–aminosalicyclic acid. Clinical symptoms disappeared rapidly and laboratory data became normal. We thus report a rare case of early-stage Crohn's disease initially indicated by biopsy of minute esophageal erosions. (Dig Endosc 1999; 11: 255–258) 相似文献
30.
Yuka MATSUMOTO Tsunao OH-I Ayako NAGAI Fuminori OHYAMA Tsuyoshi OOISHI Ryoji TSUBOI 《The Journal of dermatology》2009,36(2):98-102
We report a case of cutaneous infection due to Scedosporium apiospermum in a 75-year-old immunocompromised male patient who had received long-term corticosteroid and immunosuppressant therapy for the treatment of nephrotic syndrome. The patient came to our department complaining of erythema with a number of pustules on the dorsal surface of the right hand. S. apiospermum was identified from a culture taken from the pus. After unsuccessful treatment with topical ketoconazole, oral itraconazole and oral terbinafine, the lesion quickly resolved with the daily administration of 400 mg voriconazole. No recurrence was observed despite discontinuation of voriconazole due to drug-induced hepatitis. Voriconazole holds out the promise of an effective treatment for invasive Scedosporium infection. 相似文献