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Houda Ben Ayed Sourour Yaïch Maïssa Ben Jmaa Jihene Jedidi Mariem Ben Hmida Maroua Trigui Mondher Kassis Raouf Karray Yosra Mejdoub Habib Feki Jamel Damak 《Pediatrics international》2018,60(1):76-82
Background
The aim of this study was to describe the epidemiological profile of childhood respiratory tract diseases (RTD) in the region of Sfax, Tunisia, and to evaluate their trends over a 13 year period.Methods
We conducted a retrospective study of all children hospitalized with RTD aged under 14 years. We collected data from the regional morbidity register of the university hospital of Sfax from 2003 to 2015.Results
A total of 10 797 RTD patients were enrolled from 49 880 pediatric hospitalizations (21.7%). A male predominance was noted (60%). The median age was 8 months (IQR, 2–36 months). Acute bronchitis (AB) accounted for 53.8%, followed by asthma (15%), pneumonia (14%) and acute upper respiratory infection (AURI; 7.2%). The hospital incidence rate (HIR) of RTD was 34/10 000 inhabitants/year. It was 18.2; 5.07; 4.7 and 2.4/10 000 inhabitants for AB, asthma, pneumonia and AURI, respectively. We noted a significant increase in the HIR of RTD with an annual percentage change (APC) of 10.94% (P < 0.001); in the HIR of AB (APC, 5.27%; P < 0.001); and in asthma HIR (APC, 11.2%; P < 0.001). Otherwise, a significant decrease in AURI HIR was observed (APC, –8.8%; P < 0.001). AB lethality rate increased significantly, with an APC of 7.4% (P < 0.001). Projected trends analysis up to 2024 showed a significant rise in AB and in asthma, while AURI would significantly decrease.Conclusions
RTD continues to be a serious health problem over time in terms of morbidity and mortality. Preventive and curative strategies are needed urgently. 相似文献103.
Bennour A Sennana H Zaier M Ouahchi I Mrad Z Ben Youssef Y Khelif A Saad A 《Medical oncology (Northwood, London, England)》2012,29(2):1134-1136
Sex chromosomes are infrequently involved in patients with hematologic malignancies. In most instances, the abnormality is
either duplication in the q arm or deletion and translocation involving the q13 and q24 regions. We report herein a rare translocation
t(X;10)(p10;p10) in a newborn with 2 months and 20 days with acute myeloid leukemia (AML) (FAB, M4). Cytogenetic analysis
detected a cell clone with t(X;10)(p10;p10). Thus was confirmed by FISH analysis with whole chromosome painting (WCP) specific
for chromosomes X and 10. The patient was treated with chemotherapy, and a complete morphologic and cytogenetic remission
was achieved. To our knowledge, our case is the first report of a neonatal AML4 with t(X; 10). The patient had an excellent
early response to a salvage AML-type therapy. The prognostic significance of the t(X; 10) in this setting remains unclear.
Due to the rarity of this translocation, further cytogenetic and molecular biologic studies are required to elucidate the
clinical and molecular significance of this unusual karyotypic finding. 相似文献
104.
Bellil K Haouet S Ouertani L Trabelsi S Bouraoui S Zidi Y Chatti S Zitouna M Kchir N 《La Tunisie médicale》2002,80(1):37-39
Actinomycosis is a chronic suppurative granulomatous disease caused by an anaerobic Gram positive germ, Actinomyces. From 1994 to 1999, 21 cases of actinomycosis have been diagnosed in our laboratory. The main localisations were cervicofacial and gynecologic the diagnosis relies on histopathologic examination that shows actinomycosic granules. 相似文献
105.
Autoimmune hepatitis and primary biliary cirrhosis are two different liver diseases. The aim of this study is to relate the clinical, serologic and histologic features of patients presenting the overlap syndrome, and to evaluate their response to therapy. This is a retrospective study concerning patients presenting overlap syndrome diagnosed between january 1998 and December 2001. Five patients fulfilled the diagnosis criteria of overlap syndrome. The optimal type of treatment of the overlap syndrome was not known. Treatment with UDCA or immunosuppressor alone are not efficient. Combination of these drugs should be evaluated in further studies. 相似文献
106.
Amr Mahmoud Abdel Samad Abeer Abdelzaher Ibrahim Yosra Abdelzaher Ibrahim 《The Egyptian Journal of Radiology and Nuclear Medicine》2018,49(4):1155-1158
Objectives
To evaluate the efficacy and safety of percutaneous cholecystostomy (PC) in management of acute cholecystitis in elderly patients.Methods
Retrospective study of elderly patients (age?≥?60?years) undergoing Ultrasound-guided PC for acute cholecystitis, over a period of two years. Patients were reviewed for demographic features, co-morbidity, resolution of symptoms and outcome and complications.Results
Seventeen patients (11 women, 6 men; mean age, 66?±?7?years) underwent PC for acute cholecystitis. PC was technically successful in all patients and showed positive clinical response within 72?h in 15 patients (88.2%). Complications of PC tube placement occurred in 2 (11.8%) of 17 patients, including bile leakage around the skin in 1 patient ,tube dislodgment in another one and were treated effectively with drain replacement.Conclusion
Percutaneous cholecystostomy is a safe, effective and technically achievable procedure for treating elderly high-risk patients who present with acute cholecystitis. 相似文献107.
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Independent association of PD‐L1 expression with noninactivated VHL clear cell renal cell carcinoma—A finding with therapeutic potential
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Solène‐Florence Kammerer‐Jacquet MD Laurence Crouzet MD Angélique Brunot MBBS Julien Dagher MD Adélaïde Pladys Julien Edeline MD PhD Brigitte Laguerre MD Benoit Peyronnet MD Romain Mathieu MD Grégory Verhoest MD Jean‐Jacques Patard MD PhD Alexandra Lespagnol MD Jean Mosser MD PhD Marc Denis MD PhD Yosra Messai PhD Sophie Gad‐Lapiteau PhD Salem Chouaib PhD Marc‐Antoine Belaud‐Rotureau PharmD PhD Karim Bensalah MD PhD Nathalie Rioux‐Leclercq MD 《International journal of cancer. Journal international du cancer》2017,140(1):142-148
Clear cell renal cell carcinoma (ccRCC) is an aggressive tumor that is characterized in most cases by inactivation of the tumor suppressor gene VHL. The VHL/HIF/VEGF pathway thus plays a major role in angiogenesis and is currently targeted by anti‐angiogenic therapy. The emergence of resistance is leading to the use of targeted immunotherapy against immune checkpoint PD1/PDL1 that restores antitumor immune response. The correlation between VHL status and PD‐L1 expression has been little investigated. In this study, we retrospectively reviewed 98 consecutive cases of ccRCC and correlated PD‐L1 expression by immunohistochemistry (IHC) with clinical data (up to 10‐year follow‐up), pathological criteria, VEGF, PAR‐3, CAIX and PD‐1 expressions by IHC and complete VHL status (deletion, mutation and promoter hypermethylation). PD‐L1 expression was observed in 69 ccRCC (70.4%) and the corresponding patients had a worse prognosis, with a median specific survival of 52 months (p = 0.03). PD‐L1 expression was significantly associated with poor prognostic factors such as a higher ISUP nucleolar grade (p = 0.01), metastases at diagnosis (p = 0.01), a sarcomatoid component (p = 0.04), overexpression of VEGF (p = 0.006), and cytoplasmic PAR‐3 expression (p = 0.01). PD‐L1 expression was also associated with dense PD‐1 expression (p = 0.007) and with ccRCC with 0 or 1 alteration(s) (non‐inactivated VHL tumors; p = 0.007) that remained significant after multivariate analysis (p = 0.004 and p = 0.024, respectively). Interestingly, all wild‐type VHL tumors (no VHL gene alteration, 11.2%) expressed PD‐L1. In this study, we found PD‐L1 expression to be associated with noninactivated VHL tumors and in particular wild‐type VHL ccRCC, which may benefit from therapies inhibiting PD‐L1/PD‐1. 相似文献