A Prospective, Randomized, Multicenter Food and Drug Administration Investigational Device Exemptions Study of Lumbar Total Disc Replacement With the CHARITE^<TM> Artificial Disc Versus Lumbar Fusion : Part I : Evaluation of Clinical Outcomes

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概要

• 論文の詳細を見る
• 2005-07-15

著者

• Mcafee Paul

  Spine And Scoliosis Center St. Joseph's Hospital

• BLUMENTHAL Scott

  Texas Back Institute

• GUYER Richard

  Texas Back Institute

• REGAN John

  Cedars Sinai Spine Center

• Regan John

  West Coast Spine Institute

• GEISLER Fred

  Illinois Neuro-Spine Center

• Garcia Rolando

  Aventura Hospital And Medical Center

• HOCHSCHULER Stephen

  Texas Back Institute

• HOLT Richard

  Spine Surgery, PSC

• OHNMEISS Donna

  Texas Back Institute Research Foundation

• Holt Richard

  Spine Surgery Psc

• Ohnmeiss Donna

  Texas Back Institute Musculoskeletal Research Foundation Texas Health Research Institute

• Regan John

  Cedar Sinai Institute For Spinal Disorders

関連論文

• Evaluation of Surgical Volume and the Early Experience With Lumbar Total Disc Replacement as Part of the Investigational Device Exemption Study of the Charite Artificial Disc
• Biomechanical Analysis of Rotational Motions After Disc Arthroplasty : Implications for Patients With Adult Deformities
• Porous Coated Motion Cervical Disc Replacement : A Biomechanical, Histomorphometric, and Biologic Wear Analysis in a Caprine Model
• Revisability of the CHARITE Artificial Disc Replacement : Analysis of 688 Patients Enrolled in the U.S. IDE Study of the CHARITE Artificial Disc
• Multidirectional flexibility analysis of anterior and posterior lumbar artificial disc reconstruction: in vitro human cadaveric spine model.
• A Prospective, Randomized, Multicenter Food and Drug Administration Investigational Device Exemption Study of Lumbar Total Disc Replacement With the CHARITE^ Artificial Disc Versus Lumbar Fusion : Part II : Evaluation of Radiographic Outcomes and Corr
• A Prospective, Randomized, Multicenter Food and Drug Administration Investigational Device Exemptions Study of Lumbar Total Disc Replacement With the CHARITE^ Artificial Disc Versus Lumbar Fusion : Part I : Evaluation of Clinical Outcomes
• Adjacent Level Intradiscal Pressure and Segmental Kinematics Following A Cervical Total Disc Arthroplasty : An In Vitro Human Cadaveric Model
• The Indications for Interbody Fusion Cages in the Treatment of Spondylolisthesis : Analysis of 120 Cases
• Multidirectional flexibility analysis of cervical artificial disc reconstruction: in vitro human cadaveric spine model.
• A Prospective, Randomized, Multicenter Food and Drug Administration Investigational Device Exemption Study of Lumbar Total Disc Replacement With the CHARITE^ Artificial Disc Versus Lumbar Fusion : Part II : Evaluation of Radiographic Outcomes and Corr
• Experimental Design of Total Disk Replacement-Experience with a Prospective Randomized Study of the SB Charite
• Analysis of Porous Ingrowth in Intervertebral Disc Prostheses : A Nonhuman Primate Model
• Letters
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• A New Computer-Aided Technique for Analysis of Lateral Cervical Radiographs in Postoperative Patients With Degenerative Disease
• Traumatic Thoracic ASIA A Examinations and Potential for Clinical Trials
• The Natural History of Polyethylene Oxidation in Total Disc Replacement
• Complement Membrane Attack Complexes in Pathologic Disc Tissues
• Intervertebral Disc Prostheses
• Repeatability of Pain Drawings in a Low Back Pain Population
• Comparison of Results of Total Disc Replacement in Postdiscectomy Patients Versus Patients With No Previous Lumbar Surgery
• Effect of Adverse Events on Low Back Surgery Outcome : Twenty-Four-Month Follow-up Results From a Food and Drug Administration Investigational Device ExemptionTrial
• Minimally Invasive Surgery : Lateral Approach Interbody Fusion : Results and Review
• Endoscopic Lateral Transpsoas Approach to the Lumbar Spine
• Oxiplex Reduces Leg Pain, Back Pain, and Associated Symptoms After Lumbar Discectomy
• LETTERS

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