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101.
102.
Gonca G. Bural Drew A. Torigian Anne Burke Mohamed Houseni Khaled Alkhawaldeh Andrew Cucchiara Sandip Basu Abass Alavi 《Molecular imaging and biology》2010,12(3):233-239
Aims and Objectives
The aim of this study was to compare hepatic standardized uptake values (SUVs) and hepatic metabolic volumetric products (HMVP) between patients of diffuse hepatic steatosis and control subjects with normal livers. 相似文献103.
Pseudo-Kaposi sarcoma is a rare vascular phenomenon which can be related to congenital vascular malformations or acquired venous insufficiency. The differential diagnosis includes Kaposi sarcoma. In this report, a patient with Pseudo-Kaposi sarcoma Stewart-Bluefarb subtype is presented and the related literature is reviewed. 相似文献
104.
Determination of renal neoplasms, hematoma, infarct, urinoma, cysts, and pyelonephritis may require contrast material administration
following unenhanced CT in patients with flank pain. In this pictorial review, we aimed to clarify when contrast material
administration is needed following vague urinary system findings on unenhanced CT.
Erhan Akpinar and Baris Turkbey contributed equally to this work. 相似文献
105.
106.
Inan UU Yilmaz MD Demir Y Degirmenci B Ermis SS Ozturk F 《International journal of pediatric otorhinolaryngology》2006,70(7):1307-1314
We describe a family with lacrimo-auriculo-dento-digital syndrome (LADD). A 13-year-old boy had cup-shaped ears, deafness, unilateral choanal atresia, bilateral nasolacrimal duct obstruction, xerostomia, alacrima due to congenital absence of lacrimal glands, agenesis of salivary glands, chronic dacryocystitis, keratoconjunctivitis sicca, ptosis, nail dysplasia of the thumb, shortness of fifth toe, temporal bone abnormality and epilepsy. His younger sister had shortened middle phalanx of fifth digits. His middle sister had hypodontia, shortened distal phalanx of fifth digit, agenesis of salivary glands, mild hearing loss and exotropia. His older sister had left nasolacrimal duct obstruction and aplasia of both parotid glands. The oldest sister had hypodontia and divergent excess exotropia. His mother had hypodontia. These findings are consistent with LADD syndrome. An autosomal dominant pattern of inheritance with variable expressivity has been demonstrated. Renal and uro-genital anomalies have been noted variably. 相似文献
107.
Seher Demirer Neriman Sengül Aydin Inan Aydan Eroglu Cihan Bumin Ercüment Kuterdem 《Journal of investigative surgery》2013,26(4):221-225
The purpose of this study was to investigate the efficacy of recombinant human granulocyte/macrophage colony-stimulating factor (rHuGM-CSF) on the wound healing of colonic anastomosis in rats. In total, 40 male Wistar rats were taken into this study. The control group (n = 20) received subcutaneous saline injection. The experiment group (n 相似文献
108.
Suna
zhan Oktar Devrim Karaosmanolu Cem Yücel Gonca Erba Aydan Ilkme Ilksen Canpolat Hakan
zdemir 《Journal of ultrasound in medicine》2006,25(8):1051-1058
OBJECTIVE: Portomesenteric venous gas is a rare condition with an unclear pathogenesis. Most studies in the medical literature mention computed tomography (CT) as the primary imaging tool for this entity. The objective of this study was to outline the advantages and disadvantages of sonography in the evaluation of patients with portomesenteric venous gas. METHODS: We describe 7 patients (3 female and 4 male; age range, 47-83 years) with portomesenteric venous gas. Both CT and sonographic examinations were performed in each patient. Our patient population consisted of 2 patients with superior mesenteric artery occlusion, 3 with ischemia of the colon, small bowel, or both, 1 with gastric ulcer perforation, and 1 with ischemic bowel disease presumably secondary to complications of continuous ambulatory peritoneal dialysis. RESULTS: Portal venous gas was observed in all 7 patients with sonography and in 6 patients with CT. Computed tomography was unable to show gas in the portal venous system in 1 patient. Sonography showed patchy hepatic gas accumulation (likely within small peripheral portal vein branches) with no correlative findings on CT. Computed tomography showed important associated findings, including pneumatosis intestinalis. CONCLUSIONS: In cases with portomesenteric gas, CT is the preferred modality for showing the underlying etiology. However, with its real-time imaging capability, sonography may also be a very valuable imaging modality in the evaluation of this entity. 相似文献
109.
Brucellosis is a zoonotic disease and virtually all infections derived from exposure to animals or ingestion of unpasteurized dairy products. Brucellosis among family members has been reported. However, screening household members of an index case of acute brucellosis is not a routine procedure. A 10-y-old boy was diagnosed with acute brucellosis. Unpasteurized goat cheese commonly consumed within the family was thought to be the possible source of the bacteria. The family (parents, sister and brother) was screened with physical examination, serum tube agglutination test, blood cultures and routine laboratory tests. Three additional cases (parents and sister) of serological and culture proven brucellosis were detected. Two of them (mother and sister) were asymptomatic and had no clinical findings. Brucella melitensis biovar 3 was isolated from breast milk culture and from all blood cultures of 4 brucellosis cases. In conclusion, brucellosis, even with bacteraemia, can be completely asymptomatic. Consumption of raw milk products by household members is a common risk factor for brucellosis outbreak among family members. Thus, screening household members of an index case of brucellosis can expose new brucellosis cases. 相似文献
110.
Karakilic Ersen Saygili Emre Sedar Silan Fatma Onduc Gonca Gul Agcaoglu Ugurcan 《International journal of diabetes in developing countries.》2022,42(4):703-712
International Journal of Diabetes in Developing Countries - Although monogenic diabetes accounts for a small proportion of diabetes cases, accurate diagnosis may significantly change treatment.... 相似文献