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排序方式: 共有159条查询结果,搜索用时 15 毫秒
41.
Duygu Geler Kulcu Berfu Akbas Beyza Citci Mutlu Cihangiroglu 《The journal of spinal cord medicine》2009,32(2):198-203
Background/Objective:
To report manifestation of autonomic dysreflexia (AD) in a man with multiple sclerosis (MS).Design:
Case report.Findings:
A young man presented with a history of several admissions to the emergency department with complaints of hypertensive attacks, palpitations, difficulty in breathing, headaches, and flushing. The attacks were attributed to a previously diagnosed anxiety disorder. Onset of numbness of the left leg numbness prompted a more thorough study, which showed evidence of MS. AD was suspected as the cause of his recurrent attacks of hypertension. Bladder distension was identified as the cause of AD, and his hypertensive attacks were controlled by management of neurogenic bladder.Conclusions:
This report emphasizes that AD can occur in MS. Somatic symptoms warrant thorough investigation before attributing them to psychosomatic causes. 相似文献42.
Background Maxillonasal dysplasia (Binder’s syndrome) is a congenital malformation characterized by an extremely flat and retruded nose.
Methods This report describes an 18-year-old woman with maxillonasal dysplasia (Binder’s syndrome). The septal deficiencies and maxillary
retrusion of the patient were corrected by using an L-shaped implant and a crescent-shaped high-density porous polyethylene
implant through the oral vestibular sulcus via an external rhinoplasty approach.
Results After the operation, the tip of the nose had moved 5.5 mm anteriorly in the sagittal plane and 11.9 mm coronally in the vertical
plane. Also, the nasolabial angle had increased after the surgery. Follow-up evaluation at 24 months showed good correction
of the nasal and midface projection.
Conclusions High-density porous polyethylene implants are a good alternative for patients with Binder’s syndrome, especially those who
will not accept costal cartilage grafts or orthognathic surgery and who have tendency for hypertrophic scarring. 相似文献
43.
Akdag B Fenkci S Degirmencioglu S Rota S Sermez Y Camdeviren H 《Advances in therapy》2006,23(6):885-892
Most current statistical strategies for determining risk factors for hypertension (HT) among certain populations have proved
inconclusive. In this study, the classification tree method, which is more practical and easy to understand than other statistical
methods, was used to determine the risk for HT among outpatients in a clinic in Denizli province, western Turkey, between
January 2002 and July 2004. The effects of 14 risk factors (body mass index, waist-to-hip ratio, age, serum total cholesterol,
serum triglycerides, sex, HT in first-degree relatives, diabetes mellitus, smoking, stress factors, alcohol consumption, dyslipidemia
in first-degree relatives, dyslipidemia [previously diagnosed], and saturated fat consumption) on HT were evaluated in this
population. In all, 1761 adults at the outpatient clinic were recruited for lipid and HT measurements. The classification
tree method revealed 7 main risk factors (body mass index, waist-to-hip ratio, sex, serum triglycerides, serum total cholesterol,
HT in first-degree relatives, and saturated fat consumption) for HT. The findings of the present study suggest that the classification
tree is a valuable statistical method for evaluating multiple risk factors for HT. 相似文献
44.
Burçin Tuncel Sedat Kaygusuz Derya Beyza Sayın Kocakap Emel Aksoy Ahmet Kürşat Azkur 《Journal of medical virology》2023,95(1):e28376
Hepatitis B virus (HBV) is still a significant health problem in human. HBV severity or sensitivity of patients may be based on the individual genetic factors significantly. The aim of this study is to investigate the association of CCR5 (CCR5Δ32), TLR3 (rs5743313) functional gene polymorphisms, interferon-gamma (IFN-ɣ) level in HBV infection, which are thought to play an important role in innate and acquired immunity in patients who have undergone HBV seroconversion and those who have chronic hepatitis B disease and receive treatment. One hundred patients who are became naturally immune against HBV infection (HBsAg negative, anti-HBc IgG, and anti-HBs IgG positive), and 100 patients with chronic hepatitis B infection (>6 months HBsAg positive) who are receiving oral antiviral therapy were compared for CCR5Δ32, TLR3 (rs5743313) genotypes and serum IFN-ɣ level. It was found that CCR5Δ32 polymorphism (Wt/Δ32 and Δ32/Δ32) was significantly higher in the chronic hepatitis B group (p = 0.048) but not for TLR3 gene polymorphism. However, serum IFN-ɣ level was significantly higher in the HBV seroconversion group (75 ± 89 ng/ml) than in the chronic hepatitis B group (4.35 ± 17.27 ng/ml) (p < 0.001). In conclusion, a higher CCR5Δ32 allele frequency in patients with chronic hepatitis B might be considered as a marker of progression to chronic hepatitis. 相似文献
45.
Objective In this study, the patients who developed asymptomatic candiduria in the intensive care unit were followed prospectively for the persistence of candiduria after the replacement of indwelling urethral catheter and the correlation between persistence and virulence factors (proteinase enzyme activity and epithelial adhesion) was assessed.Design Prospective study.Setting Intensive care unit and mycology laboratory at a university hospital.Patients Thirty-four patients with asymptomatic candiduria were included in the study.Results Candiduria persisted in 19 of 34 patients(56%; group 1) and cleared in 15 of 34 patients(44%; group 2) after urinary catheters were changed. When the virulence factors (epithelial adhesion and proteinase activity) and distribution of Candida spp. were compared between two groups, no statistically significant correlation was found.Conclusion The host immune response might be more important than virulence factors of Candida spp. for persistence of candiduria. 相似文献
46.
Leili Jalili-Baleh Hamid Nadri Hamid Forootanfar Tuba Tüylü Küükkln Beyza Ayazgk Mohammad Sharifzadeh Mahban Rahimifard Maryam Baeeri Mohammad Abdollahi Alireza Foroumadi Mehdi Khoobi 《Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences》2021,29(1):23
PurposeAlzheimer’s disease (AD) is a multifaceted neurodegenerative disease. To target simultaneously multiple pathological processes involved in AD, natural-origin compounds with unique characteristics are promising scaffolds to develop novel multi-target compounds in the treatment of different neurodegenerative disease, especially AD. In this study, novel chromone-lipoic acid hybrids were prepared to find a new multifunctional lead structure for the treatment of AD.MethodsChromone-lipoic acid hybrids were prepared through click reaction and their neuroprotection and anticholinesterase activity were fully evaluated. The anti-amyloid aggregation, antioxidant and metal-chelation activities of the best compound were also investigated by standard methods to find a new multi-functional agent against AD.ResultsThe primary biological screening demonstrated that all compounds had significant neuroprotection activity against H2O2-induced cell damage in PC12 cells. Compound 19 as the most potent butyrylcholinesterase (BuChE) inhibitor (IC50 = 7.55 μM) having significant neuroprotection activity as level as reference drug was selected for further biological evaluations. Docking and kinetic studies revealed non-competitive mixed-type inhibition of BuChE by compound 19. It could significantly reduce formation of the intracellular reactive oxygen species (ROS) and showed excellent reducing power (85.57 mM Fe+2), comparable with quercetin and lipoic acid. It could also moderately inhibit Aβ aggregation and selectively chelate with copper ions in 2:1 M ratio.ConclusionCompound 19 could be considered as a hopeful multifunctional agent for the further development gainst AD owing to the acceptable neuroprotective and anti-BuChE activity, moderate anti-Aβ aggregation activity, outstanding antioxidant activity as well as selective copper chelation ability.Graphical abstractOpen in a separate windowA new chromone–lipoic acid hybrid was synthesized as anti-Alzheimer agent with BuChE inhibitory activity, anti-Aβ aggregation, metal-chelation and antioxidant properties.Supplementary InformationThe online version contains supplementary material available at 10.1007/s40199-020-00378-1. 相似文献
47.
Is the extraction by Whatman FTA filter matrix technology and sequencing of large ribosomal subunit D1–D2 region sufficient for identification of clinical fungi? 下载免费PDF全文
Nuri Kiraz Yasemin Oz Huseyin Aslan Zayre Erturan Beyza Ener Sevtap Arikan Akdagli Hamza Muslumanoglu Zafer Cetinkaya 《Mycoses》2015,58(10):588-597
Although conventional identification of pathogenic fungi is based on the combination of tests evaluating their morphological and biochemical characteristics, they can fail to identify the less common species or the differentiation of closely related species. In addition these tests are time consuming, labour‐intensive and require experienced personnel. We evaluated the feasibility and sufficiency of DNA extraction by Whatman FTA filter matrix technology and DNA sequencing of D1–D2 region of the large ribosomal subunit gene for identification of clinical isolates of 21 yeast and 160 moulds in our clinical mycology laboratory. While the yeast isolates were identified at species level with 100% homology, 102 (63.75%) clinically important mould isolates were identified at species level, 56 (35%) isolates at genus level against fungal sequences existing in DNA databases and two (1.25%) isolates could not be identified. Consequently, Whatman FTA filter matrix technology was a useful method for extraction of fungal DNA; extremely rapid, practical and successful. Sequence analysis strategy of D1–D2 region of the large ribosomal subunit gene was found considerably sufficient in identification to genus level for the most clinical fungi. However, the identification to species level and especially discrimination of closely related species may require additional analysis. 相似文献
48.
Dilek Ulubas Isik Beyza Ozcan Ulker Celik Ozge Aydemir Kadri Murat Erdogan Emre Hekimoglu Ahmet Yagmur Bas Nihal Demirel 《European journal of pediatrics》2014,173(4):545-546
A variety of diseases can cause vesicular or pustular eruptions in newborns. A thorough clinical history and physical exam provide important clues for differential diagnosis. Goltz syndrome, also known as focal dermal hypoplasia, is a rare genodermatosis and generally diagnosed by the presence of the characteristic skin lesions. We present an infant with aplasia cutis, atrophic skin lesions, syndactyly and eye abnormalities who was diagnosed with Goltz syndrome soon after birth. Goltz syndrome should be considered in differential diagnosis of hypoplastic or aplastic skin lesions in neonates in the presence of skeletal or ophthalmic anomalies. 相似文献
49.
50.
Ali Akal Turgay Ulas Tugba Goncu Ekrem Karakas Omer Karakas Fatih Kurnaz Fatima Nurefsan Boyaci Omer Faruk Yilmaz Abdulgafur Bata Sema Yildiz 《Indian journal of ophthalmology》2014,62(6):671-674