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    • 1. 发明授权
    • Method and apparatus for quantitative and comparative analysis of image intensities in radiographs
    • 用于定量和比较分析影像强度的方法和装置
    • US07835559B1
    • 2010-11-16
    • US11741657
    • 2007-04-27
    • David J. SchurmanRobert Lane Smith
    • David J. SchurmanRobert Lane Smith
    • G06K9/00G01N23/05
    • G01N23/04G01N2223/302G01N2223/6123G06T7/0014G06T2207/10116G06T2207/30008
    • A system for determining image intensity of a radiograph includes an illuminator for providing lighting to the radiograph, an image reference standard having a predetermined color, a digital imaging device for obtaining a digital image of the radiograph and the image reference standard, a computer for receiving and storing the digital image and for executing programs, and an image analysis program being executed on the computer for providing a first image intensity value of a target area in the radiograph and a second image intensity value of the image reference standard and for computing a normalized image intensity value of the target area using the first and second image intensity values. In one embodiment, the image reference standard is an image reference standard of a black color or a white color.
    • 一种用于确定X射线照片的图像强度的系统包括:用于向射线照片提供照明的照明器,具有预定颜色的图像参考标准,用于获得射线照片的数字图像的数字成像装置和图像参考标准;用于接收的计算机 以及存储数字图像和用于执行程序的图像分析程序,以及在计算机上执行的图像分析程序,用于提供放射照相中的目标区域的第一图像强度值和图像参考标准的第二图像强度值,并且用于计算标准化 使用第一和第二图像强度值的目标区域的图像强度值。 在一个实施例中,图像参考标准是黑色或白色的图像参考标准。
    • 4. 发明授权
    • Method for in vivo ex vivo and in vitro repair and regeneration of cartilage and collagen and bone remodeling
    • 体外离体和体外修复和再生软骨和胶原和骨重塑的方法
    • US06528052B1
    • 2003-03-04
    • US09677109
    • 2000-09-29
    • R. Lane SmithDennis R. CarterDavid J. Schurman
    • R. Lane SmithDennis R. CarterDavid J. Schurman
    • C12N500
    • C12N5/0655A61F2/08A61F2/28A61F2/30756A61F2/3094A61F2240/001A61F2310/00365A61K35/12A61K35/32C12N2500/02C12N2521/00
    • A method for in vivo, ex vivo and in vitro regeneration of cartilage and collagen. In vivo, ex vivo and in vitro regeneration and de novo formation of articular cartilage and collagen by intermittently applied hydrostatic pressure. The application of external interval loading consisting of repeated periods of applied hydrostatic pressure followed and interrupted by periods of recovery. The application of the intermittent hydrostatic pressure at physiological levels 5-10 MPA for an interval of 4 hours followed by a recovery period up to about 20 hours, said pressure applied to the cartilage cells in vitro, explants of cartilage ex vivo and in vivo to cartilage that remains intact within te joint space of diarthrotic joints. The interval loading results in the selective inhibition of matrix degrading enzymes, pro-inflammatory cytokines and chemokines that attract inflammatory cells into the joint cavity and in selective decrease of gene, expression of growth factors that are inhibitory to type II collagen expression.
    • 一种体内,体外和体外再生软骨和胶原蛋白的方法。 通过间歇施加的静水压力,体内,离体和体外再生和从头形成关节软骨和胶原。 外部间隔负荷的应用由反复施加的静水压力组成,随后由复原期间中断。 在生理水平5-10MPA下间歇4小时的间歇静水压力的应用,随后的恢复期直到约20小时,所述压力在体外施加于软骨细胞,体外离体外植体和体内至软体 在关节关节的关节间隙内保持完整的软骨。 间隔负荷导致基质降解酶,促炎细胞因子和趋化因子的选择性抑制,其吸引炎症细胞进入关节腔,并选择性降低基因,抑制II型胶原表达的生长因子的表达。
    • 5. 发明授权
    • Articulated prosthetic knee and method for implanting same
    • 铰接假肢膝盖及其植入方法
    • US4358859A
    • 1982-11-16
    • US81713
    • 1979-10-04
    • David J. SchurmanRobert L. Piziali
    • David J. SchurmanRobert L. Piziali
    • A61F2/38A61F1/03
    • A61F2/3845
    • An articulated knee prosthesis in which a femoral implant has a condyle section and a femoral stem that is cemented into the femur. A tibial implant carries a tibial plateau section on which is mounted a stop plate for engaging the condyle section and arresting movement of the knee beyond its fully extended position. The tibial implant includes a tibial stem that is cemented into the tibia. A pivotal connection between the two implants is positioned posteriorly of the implant and at an elevation above a lowermost point of the condyle section (when the implants are fully extended). The pivot axis of the connection and the stems are positioned with respect to each other so that upon the implantation of the implant, the patient's tibia is moved in an anterior direction as compared to the normal anatomical position of the tibia relative to the femur. At least a portion of the hinged connection, which frequently includes the pivot axis, is located posteriorly of portions of the femur proximate the knee joint to maximize the arc through which the knee can be flexed.
    • 一种关节膝关节假体,其中股骨植入物具有骨髁部分和股骨柄,该股骨柄被胶合到股骨中。 胫骨植入物携带胫骨平台部分,其上安装有止动板用于接合髁部分并阻止膝盖移动到其完全伸出位置。 胫骨植入物包括胫骨柄,其被固定到胫骨中。 两个植入物之间的枢转连接位于植入物的后方并且位于髁部分的最低点之上(当植入物完全延伸时)的高度。 连接件和杆的枢转轴线相对于彼此定位,使得在植入物植入时,与胫骨相对于股骨的正常解剖位置相比,患者的胫骨在前方向上移动。 经常包括枢转轴线的铰链连接的至少一部分位于靠近膝盖关节的股骨部分的后方,以最大限度地使得膝盖能弯曲的电弧最大化。