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选育适应性强的普及玉米杂种

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国外作物育种 1997年第3期16卷 42-50页

作者： Troy.,af 向平

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模拟非均质油藏采收率的动态方法

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采油工艺情报 1995年第3期 1-6页

作者：伊斯.,af 王超

建议用一种新的动态方程组来描述在采油过程中油藏多孔介质里的压力分布。该方程组与注入井和生产井的分布一起说明油藏特性和边界条件。它解答了在油藏模拟晶格的任何位置油藏压力与时间的关系。

关键词：模拟非均质油藏采油率动态方程

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Hydraulic Circuit Design and Dynamic Learning Using Case-based Reasoning

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Computer Aided Drafting,Design and Manufacturing 2000年第1期10卷 9-16页

作者： C.M. Vong and PK. Wong (Faculty of Science and Technology, University of maca. P.O. Box 3001, Micau E-mail fstcmvumac mo Fax:(853) 838314 Tel: (853) 397476)

This paper describes the design and implementation of a hydraulic circuit design system using case-based reasoning (CBR) paradigm from AI community The domain of hydraulic circuit design and case-based reasoning are briefly reviewed Then a proposed methodology in compuer-aided circuit design and dynamic leaning with the use of CBR is described Finally an application example is selected to illustrate the ussfulness of applying CBR in hydraulic circuit design with leaming.

关键词： hydraulic circuit design case-based reasoning(CBR),dynamic learning

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Triamcinolone improves viscosupplementation

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中华物理医学与康复杂志 2013年第5期35卷 413-413页

作者： De Campos GC Rezende MU Pailo af

BACKGROUND AND OBJECTIVE Intra-articular injections have been used for many years to treat patients with osteoarthritis (OA).Viscosupplementation(VS) is a relatively new intervention,with widespread use among patients with knee *** injectant is reported to relieve pain,but is also considered to be a disease modifying *** studies have shown that the effect of this medication may occur within two to five weeks after the ***,this study was designed to determine whether the addition of steroids could improve early relief and long-term *** This study included 104 patients diagnosed with knee OA,all of whom were random-

关键词：关节炎类固醇膝关节疼痛针剂

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Expanding etiology of progressive familial intrahepatic cholestasis

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World Journal of Hepatology 2019年第5期11卷 450-463页

作者： Sarah af Henkel Judy H Squires Mary Ayers Armando Ganoza Patrick Mckiernan James E Squires Division of Gastroenterology Hepatologyand NutritionEmory School of MedicineAtlantaGA 30322United States Department of Radiology UPMC Children’s Hospital of PittsburghPittsburghPA 15224United States Division of Gastroenterology Hepatologyand NutritionUPMC Children’s Hospital of PittsburghPittsburghPA 15224United States Division of Pediatric Transplantation Department of SurgeryUPMC Children’s Hospital of PittsburghPittsburghPA 15224United States

BACKGROUND Progressive familial intrahepatic cholestasis(PFIC)refers to a disparate group of autosomal recessive disorders that are linked by the inability to appropriately form and excrete bile from hepatocytes,resulting in a hepatocellular form of *** the diagnosis of such disorders had historically been based on pattern recognition of unremitting cholestasis without other identified molecular or anatomic cause,recent scientific advancements have uncovered multiple specific responsible *** variety of identified defects has resulted in an ever-broadening phenotypic spectrum,ranging from traditional benign recurrent jaundice to progressive cholestasis and end-stage liver *** To review current data on defects in bile acid homeostasis,explore the expanding knowledge base of genetic based diseases in this field,and report disease characteristics and *** We conducted a systemic review according to PRISMA *** performed a Medline/PubMed search in February-March 2019 for relevant articles relating to the understanding,diagnosis,and management of bile acid homeostasis with a focus on the family of diseases collectively known as *** only articles were accessed in *** manual search included references of retrieved *** extracted data on disease characteristics,associations with other diseases,and *** was summarized and presented in text,figure,and table *** Genetic-based liver disease resulting in the inability to properly form and secrete bile constitute an important cause of morbidity and mortality in children and increasingly in adults.A growing number of PFIC have been described based on an expanded understanding of biliary transport mechanism defects and the development of a common *** We present a summary of current advances made in a number of areas relevant to both the classically described FIC1(ATP8B1),BSEP(ABCB11),and MDR3(ABCB4)transporter deficiencie