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排序方式: 共有435条查询结果,搜索用时 15 毫秒
1.
探讨改良式剖宫产术的临床价值。方法:采用香港周杰医师1991年创立的一套改式剖宫产术对50例产妇进行手术并与同期腹部横切口传统剖宫产术进行比较。结果:改良式剖宫产术所用时间短,术中出血小,术后排气暗暗科痛轻、产褥病发生率低。住院时间短,与对照组比较有明显差异。 相似文献
2.
Aliya Kabylbekova Serik Meirmanov Altyn Aringazina Lukpan Orazbekov Ardak Auyezova 《Annals of medicine》2022,54(1):1988
PurposeTo investigate the age at recognition and presentation for surgery for congenital and developmental cataract at Kazakh Eye Research Institute in Kazakhstan.MethodsA retrospective review of children aged 0–18 years, who presented with congenital and developmental cataract between January 1, 2010 and December 31, 2020. All medical records were reviewed. Gender, age at recognition, age at surgery, laterality, residential location (rural/urban) were recorded.ResultsThe study population included 897 patients of children presented with congenital and developmental cataract over a 10-year study period, 58% of them were boys and 44.6% were from rural areas. Cataract was bilateral in 621 (69.2%) and unilateral in 276 (30.8%) of patients. Median age at recognition for patients with congenital/developmental cataract was 12 months. Median age at surgery for congenital/developmental cataract was 51 months. Only 14.7% of children underwent surgery within first year of life. The urban citizens underwent surgery earlier than patients from rural areas. The median delay in presentation for surgery was 15 months.ConclusionThe average age at cataract surgery in the population of Kazakhstan is much older than in developed countries. It is essential to study barriers that associated with delayed presentation to build strategies to overcome them.
Key messages
- It is known that cataract surgery in children early in life provides favourable visual outcome.
- Children with congenital and developmental cataract in Kazakhstan experience delay in surgical treatment.
- Children from rural areas undergo cataract surgery later than urban citizens.
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Saeed Khan Nadeem N Jaffer Mohammad Nasherwan Khan Mohammad A Rai Majid Shafiq Adnan Ali Shahid Pervez Nusrat Khan Aliya Aziz Syed H Ali 《International journal of infectious diseases》2007,11(4):313-317
INTRODUCTION: Human papillomavirus (HPV) is recognized as a major causative agent for cervical carcinomas. Based on their oncogenic potential, HPV subtypes have been divided into high- and low-risk. In Pakistan, screening for HPV in female patients is not commonly practiced, and as a consequence, the degree of HPV prevalence and its correlation with cervical cancer is unknown. OBJECTIVE: In this study, we have attempted to estimate the prevalence of HPV infection, and also the HPV subtype profile, among Pakistani women with cervical cancer from varied geographical, racial, and social backgrounds within Pakistan. METHODOLOGY: Women visiting two tertiary care hospitals in Karachi, diagnosed with carcinoma of the cervix within the past 15 years, were analyzed for HPV subtypes in their cancer specimens. Retrospectively, 60 paraffin-embedded cervical cancer biopsies were examined for the presence of HPV DNA. After DNA extraction from these samples, polymerase chain reaction (PCR) was used to amplify the HPV L1 gene using the consensus (general) primers, and primers specific for subtypes 16 and 18. RESULTS: Of the 60 samples analyzed, only one sample was HPV negative; the rest of the samples were positive for the presence of HPV. Of the 59 HPV positive samples, 56 showed the presence of HPV16 and one sample was positive for HPV18; HPV subtype could not be determined in two samples. CONCLUSION: Our results show a strong relationship between HPV infection and cervical cancer among Pakistani women. These results underscore the need to implement regular HPV screening for Pakistani women. An early diagnosis of HPV infection will allow better health management to reduce the risk of developing cervical cancer. 相似文献
5.
A novel approach towards recognition of sulfonylureas based on a polymerisable ion pair is presented. A solution association constant >105 M−1 between the model target glibenclamide and 4-vinylbenzyltrimethylammonium methacrylate is measured, and the formation of 1 : 1 complexes verified. Subsequently prepared stoichiometrically imprinted polymers exhibit exceptionally high affinity and binding capacity for glibenclamide, owing to synergistic binding of both the neutral and deprotonated form of the drug by the ion pair monomer. The polymers are applied to the selective extraction of glibenclamide from blood serum samples, achieving recoveries of up to 98% and demonstrating excellent long-term stability, negating the need for regular sorbent regeneration.Polymerisable ion pair captures both neutral and anionic form of acidic sulfonylurea drug in stoichiometrically imprinted polymer. 相似文献
6.
Jasmine Aliya G.V. Akila Durai Vanitha M. Anitha Rani Shriraam Vanishree V. Samya T. Gayathri Mahadevan Shriraam 《International journal of diabetes in developing countries.》2021,41(2):293-300
International Journal of Diabetes in Developing Countries - There is a huge burden of diabetes-related complications, both microvascular and macrovascular, in India. With the rising prevalence of... 相似文献
7.
目的探讨DNA甲基化在肺腺癌发生中的作用机制。方法收集2019年1月至12月新疆肿瘤医院确诊的肺腺癌和正常对照者外周血各4例,850K芯片甲基化检测平台检测肺腺癌组与正常对照组甲基化区域,Bump hunter寻找两组差异区域。Gene Ontology数据库和KOBAS软件对差异区域对应目的基因进行GO分析和KEEG分析。结果1.共筛选出DMR-1、DMR-2、DMR-3、DMR-4、DMR-6(以上位于chr6),DMR-5(位于chr11)和DMR-7(位于chr20)(P<0.05)七组差异甲基化区域。DMR-1目的基因为HLA-DPB1、HLA-DPA1,DMR-2的为POU5F1,DMR-3的为RP5-1186N24.3、SCAND3,DMR-4的为ZFP57,DMR-5的为LDHC,DMR-6的为LTA,DMR-7的为OXT。其中HLA-DPB1、HLA-DPA1等为高甲基化,SCANDS3和LTA为低甲基化。2.GO分析表明目的基因主要在干扰素-γ、MHC-Ⅱ类复合物等功能中发挥重要作用。KEGG分析显示目的基因甲基化主要在Ⅰ型糖尿病、NF-κB信号通路中高度富集。结论1.肺腺癌患者DNA甲基化的状态可能是引起肺腺癌发生的关键因素,尤其是HLA-DP,POU5F1及LDHC的甲基化状态,在肺腺癌的发生中起着重要的作用。2.在GO功能和KEGG通路中,阐明了DNA甲基化异常导致疾病发展的作用机制。 相似文献
8.
Bhausaheb Bagal Arun Chandrasekharan Aliya Chougle Navin Khattry 《Hematology/oncology and stem cell therapy》2018,11(1):47-51
Objective/background
Hepatic veno-occlusive disease (VOD) is well recognized potentially serious regimen-related toxicity seen after stem cell transplantation. Severe VOD is associated with poor long-term outcomes with very high mortality. Besides supportive care, only defibrotide has been found to be effective in the management of VOD. The recommended dose of defibrotide is 25 mg/kg/d but there has been no classical dose finding study done for this drug. A higher dose of defibrotide is associated with increased risk of bleeding and this drug is prohibitively expensive. We report our experience of using fixed low dose of defibrotide in patients with VOD.Methods
We retrospectively evaluated 511 patients who underwent stem cell transplant at our center from November 2007 and December 2015. All patients received ursodeoxycholic acid as VOD prophylaxis. Modified Seattle criterion was used for diagnosis and severity grading of VOD. Patients developing VOD were initially treated with furosemide and adequate analgesia. Defibrotide was started within 12 to 24 hours of diagnosis of VOD. All adult patients received defibrotide at a fixed dose of 200 mg twice daily while two children were given dose of 100 mg and 50 mg twice daily.Results
Nine (1.7%) of our patients developed VOD. Daily dose of defibrotide ranged from 5 mg/kg/d to 20 mg/kg/d till resolution of VOD. All patients had complete resolution of VOD. None of our patients required ventilator support or dialysis. No episodes of bleeding were observed. No dose response relationship was observed between defibrotide dose and time to resolution of VOD.Conclusion
Low fixed dose defibrotide initiated early seems to be effective and safe in treatment of VOD. This is relevant in a resource limited setting and warrants prospective evaluation. 相似文献9.
Aliya Ishmukhametova Jian‐Min Chen Rafaëlle Bernard Bernard de Massy Frédéric Baudat Amandine Boyer Déborah Méchin Delphine Thorel Brigitte Chabrol Marie‐Claire Vincent Mireille Claustres Sylvie Tuffery‐Giraud 《Human mutation》2013,34(8):1080-1084
Pathogenic complex genomic rearrangements are being increasingly characterized at the nucleotide level, providing unprecedented opportunities to evaluate the complexities of mutational mechanisms. Here, we report the molecular characterization of a complex duplication–triplication rearrangement involving exons 45–60 of the DMD gene. Inverted repeats facilitated this complex rearrangement, which shares common genomic organization with the recently described duplication‐inverted triplication–duplication (DUP–TRP/INV‐DUP) events; specifically, a 690‐kb region comprising DMD exons from 45 to 60 was duplicated in tandem, and another 46‐kb segment containing exon 51 was inserted inversely in between them. Taking into consideration (1) the presence of a predicted PRDM9 binding site in the near vicinity of the junction involving two inverted L1 elements and (2) the inherent properties of X–Y chromosome recombination during male meiosis, we proposed an alternative two‐step model for the generation of this X‐linked DMD DUP–TRP/INV‐DUP event. 相似文献