![]() | John Turner SharpShow email addressMaastricht University Medical Center, Department of Internal Medicine, Subdivision of Rheumatology, Maastricht, The Netherlands. | Division of Rheumatology, University of ... |
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John Turner Sharp:Expert Impact
Concepts for whichJohn Turner Sharphas direct influence:Rheumatoid arthritis,Radiographic progression,Coronary embolism,Thoracoabdominal motion,Respiratory muscle function,Joint space width,Psoriatic arthritis,Monoclonal antibodies.
John Turner Sharp:KOL impact
Concepts related to the work of other authors for whichfor which John Turner Sharp has influence:Rheumatoid arthritis,Synovial fluid,Systemic lupus erythematosus,Necrosis factor,Rheumatic diseases,Radiographic progression,Ankylosing spondylitis.
KOL Resume for John Turner Sharp
Year | |
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2009 | Maastricht University Medical Center, Department of Internal Medicine, Subdivision of Rheumatology, Maastricht, The Netherlands. Division of Rheumatology, University of Washington, Seattle, Washington, DC, USA |
2008 | University of Washington, Seattle |
2007 | University of Washington, Seattle, Washington, USA |
2005 | University of Washington School of Medicine, Seattle, WA, USA. |
2004 | Department of Medicine, University of Washington School of Medicine, 1959 Northeast Pacific Street, Seattle, WA 98195-6428, USA |
2003 | University of Washington, Seattle, Washington, USA. |
2002 | University of Washington, School of Medicine, Seattle |
2001 | University of Washington, Seattle, WA |
2000 | 8387 NE Sumanee Place, Bainbridge Island, WA 98110 Bainbridge Island, Washington |
1998 | Emory University, Atlanta, Georgia |
1996 | Tifton Medical Center, Tifton, Georgia |
1995 | Tifton Medical Clinic, Tifton, Georgia, and Emory University School of Medicine, Atlanta, Georgia |
1993 | Tifton, Georgia Cooperative Systemic Studies of the Rheumatic Diseases group |
1991 | 712 East 18th Street, Tifton, GA 31794 University of Colorado School of Medicine, and Director, The Joe and Betty Alpert Arthritis Center at Rose Medical Center |
1988 | Staff Physician, Tifton Medical Clinic, Tifton, GA From the Rheumatoid Arthritis Criteria Subcommittee of the Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association |
1987 | From a conference sponsored, in part, by Sandoz Pharmaceuticals, April 25—28, 1985, San Francisco, CA Tifton Medical Clinic, Tifton, Georgia |
1986 | From the Department of Medicine, Pulmonary Disease Section, and the Research Service, Hines Veterans Administration Hospital, Hines, Ill., USA Department of Medicine, Joe and Betty Alpert Arthritis Center, Denver, Colorado |
1985 | Alpert Arthritis Center, 4567 East Ninth Avenue, Denver, CO 80220 Pulmonary Medicine, Hines V.A. Hospital, Hines, IL |
1983 | Professor of Medicine, Loyola Stritch School of Medicine, Maywood, Illinois |
1982 | From the Nuclear Medicine Service, Veterans Administration Hospital, Hines, Ill. Rheumatic Disease Section, Department of Internal Medicine, Baylor College of Medicine, Houston, TX and Joe and Betty Alpert Arthritis Treatment Center, Rose Medical Center, Denver, CO |
1981 | Pulmonary Medicine Section, Medical Service, Hines Veterans Administration Hospital, Hines, IL Department of Medicine, Abraham Lincoln School of Medicine, University of Illinois College of Medicine, Chicago Veterans Administration Hospital, Hines, Illinois, Argonne National Laboratories, Lemont, Illinois, USA |
1980 | Program Director, Pulmonary Medicine, Hines, V. A. Hospital; Professor of Medicine and Physiology, University of Illinois College of Medicine, Chicago, Illinois |
1979 | Section of Pulmonary Medicine, Loyola University of Chicago, Stritch School of Medicine, Maywood, and the Section of Pulmonary Medicine, Veterans Administration Hospital, Hines, Ill |
1977 | Danville Veterans Administration Hospital, Danville, Illinois 61832 Pulmonary Disease, Veterans Administration Hospital, Hines, Ill Rheumatic Disease Section and the Section of Biomedical Computing, Department of Internal Medicine, Baylor College of Medicine, Houston, Texas |
1976 | From the Pulmonary Section, Department of Medicine, Veterans Administration Hospital, Hines, Illinois and the Departments of Physiology and Medicine, University of Illinois, Chicago |
1973 | Professor of Medicine and Chief, Rheumatology Section, Department of Medicine, Baylor College of Medicine |
1972 | Professor, Department of Medicine, Baylor College of Medicine, Houston, Texas 77025 |
1971 | Department of Medicine, Baylor College of Medicine, Houston, Texas Professor of Medicine, Chief, Rheumatic Disease Section, Baylor College of Medicine, Houston, Tex 77025 |
1970 | From the Loyola University Stritch School of Medicine, Hines, Ill. U.S.A. Departments of Microbiology and Medicine, Baylor College of Medicine, 77025, Houston, Texas |
1969 | Goroka Hospital, Territory of Papua and New Guinea, Sydney Hospital Departments of Medicine and Virology, Baylor College of Medicine, Houston, Texas |
1968 | Chicago, Illinois, USA Rheumatic Disease Section, Department of Medicine, Baylor University College of Medicine, the Ben Taub General Hospital, and Houston Veterans Administration Hospital |
1967 | From the Section of Cardiology and the Cardiopulmonary Laboratory, Veterans Administration Hospital and the Department of Medicine, University of Illinois College of Medicine, Hines, Illinois |
1965 | From the Cardiopulmonary Laboratory of the Veterans Administration Hospital, Hines, Ill., USA |
1964 | Cardiopulmonary Laboratory of the Veterans Administration Hospital, Hines, Illinois, and Departments of Medicine of the University of Illinois College of Medicine and Stritch School of Medicine of Loyola University, Chicago, Illinois |
1963 | From the Cardiopulmonary Laboratories of the Veterans Administration Hospital, Hines, Illinois, and the Children's Hospital, Buffalo, New York; the Departments of Medicine of the Stritch School of Medicine, Loyola University, and the University of Illinois College of Medicine; and the Department of Pediatrics, University of Buffalo School of Medicine, Buffalo, New York. |
1961 | This work was carried out during tenure of an Established Investigatorship of the American Heart Association. Dr. Sharp's present address is the Cardiopulmonary Laboratory, Veterans Administration Hospital, Hines, Ill. From the Cardiopulmonary Laboratory, Veterans Administration Hospital, Hines, Illinois, the Department of Medicine, Stritch School of Medicine of Loyola University, the Department of Radiology, the University of Chicago School of Medicine, and the Department of Medicine, University of Illinois School of Medicine, Chicago, Illinois. |
1960 | Buffalo, New York USA |
1959 | Established Investigator of the American Heart Association and Buswell Fellow in Medicine. |
1958 | Established Investigator of the American Heart Association. |
Concept | World rank |
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20 cell strains | #1 |
classifying structural | #1 |
antigens initiation | #1 |
hypotonia orofacial muscles | #1 |
rheumatoid arthritis multicenter | #1 |
emg lung | #1 |
synovial membrane nonrheumatoid | #1 |
atrium venae cavae | #1 |
electromyography heart humans | #1 |
chemical streptokinase trichophyton | #1 |
arthritis observed | #1 |
thirtyone months | #1 |
obesity oxygen respiration | #1 |
matched controls measles | #1 |
healthy patients patient | #1 |
emg lung volume | #1 |
sequence radiographs | #1 |
dyedilution studies | #1 |
dirhythmic breathing patients | #1 |
synovialvero | #1 |
extremes cycles | #1 |
antivascular antibody | #1 |
lymphocyte proliferation initiation | #1 |
new computerbased methods | #1 |
possibility lymphocytes | #1 |
disease erosions | #1 |
early seropositive association | #1 |
placebo denosumab doses | #1 |
skin reactivity decrease | #1 |
shunt dyedilution studies | #1 |
bronchospasm theclock | #1 |
biweekly monthly intervals | #1 |
obesity electromyography | #1 |
fever dermatologic | #1 |
prevents metacarpal | #1 |
erosion scores patients | #1 |
goodpastures syndrome cyclophosphamide | #1 |
190 patients early | #1 |
81mkr regional ventilation | #1 |
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Prominent publications by John Turner Sharp
OBJECTIVE: Tumor necrosis factor (TNF) is an important proinflammatory cytokine that mediates inflammatory synovitis and articular matrix degradation in rheumatoid arthritis (RA). We investigated the ability of adalimumab, a human anti-TNF monoclonal antibody, to inhibit the progression of structural joint damage, reduce the signs and symptoms, and improve physical function in patients with active RA receiving concomitant treatment with methotrexate (MTX).
METHODS: In this multicenter, ...
Known for Adalimumab Patients | Active Rheumatoid | Physical Function | Arthritis Receiving | Factor Monoclonal |
OBJECTIVE: To compare the efficacy and safety of adalimumab plus methotrexate (MTX) versus MTX monotherapy or adalimumab monotherapy in patients with early, aggressive rheumatoid arthritis (RA) who had not previously received MTX treatment.
METHODS: This was a 2-year, multicenter, double-blind, active comparator-controlled study of 799 RA patients with active disease of < 3 years' duration who had never been treated with MTX. Treatments included adalimumab 40 mg subcutaneously every ...
Known for Combination Therapy | Adalimumab Mtx | Clinical Trial | Methotrexate Treatment | Premier Study |
OBJECTIVE: To evaluate the efficacy and safety of treatment with adalimumab, a fully human anti-tumor necrosis factor (anti-TNF) monoclonal antibody, over 48 weeks in patients with moderate to severe psoriatic arthritis (PsA).
METHODS: Patients who completed the Adalimumab Effectiveness in Psoriatic Arthritis Trial (ADEPT), a 24-week, double-blind study of adalimumab versus placebo in PsA, could elect to receive open-label adalimumab, 40 mg subcutaneously every other week after week 24. ...
Known for Adalimumab Effectiveness | Psoriatic Arthritis | Week Patients | Monoclonal Antibodies |
OBJECTIVE: To determine the relationship between radiographic progression and clinical response for adalimumab plus methotrexate (MTX) versus either monotherapy in patients with early rheumatoid arthritis (RA) in the PREMIER study.
METHODS: Patients with early RA who received adalimumab plus MTX (n = 240), adalimumab (n = 222), or MTX (n = 216) were grouped by American College of Rheumatology (ACR) response, 28-joint Disease Activity Score (DAS28), or remission-like state [tender joint ...
Known for Radiographic Progression | Methotrexate Monotherapy | Mtx Adalimumab | Monoclonal Antibodies | Rheumatoid Arthritis |
OBJECTIVE: Adalimumab, a fully human, anti-tumor necrosis factor monoclonal antibody, was evaluated for its safety and efficacy compared with placebo in the treatment of active psoriatic arthritis (PsA).
METHODS: Patients with moderately to severely active PsA and a history of inadequate response to nonsteroidal antiinflammatory drugs were randomized to receive 40 mg adalimumab or placebo subcutaneously every other week for 24 weeks. Study visits were at baseline, weeks 2 and 4, and ...
Known for Adalimumab Placebo | Humanized Arthritis | Quality Life | Patients Monoclonal Antibodies | 24 Weeks |
Two‐year, blinded, randomized, controlled trial of treatment of active rheumatoid arthritis with leflunomide compared with methotrexate
[ PUBLICATION ]
OBJECTIVE: Three 6-12-month, double-blind, randomized, controlled trials have shown leflunomide (LEF; 20 mg/day, loading dose 100 mg x 3 days) to be effective and safe for the treatment of rheumatoid arthritis (RA). This analysis of the North American trial assessed whether the clinical benefit evident at month 12 was sustained over 24 months of treatment with LEF as compared with the efficacy and safety of methotrexate (MTX), an equivalent disease-modifying antirheumatic drug, at 24 ...
Known for Lef Mtx | 24 Months | Rheumatoid Arthritis | Year Treatment | Radiographic Progression |
OBJECTIVE: To determine whether treatment with leflunomide (LEF), methotrexate (MTX), or sulfasalazine (SSZ) for 6-12 months retards progression of radiographic damage and to identify clinical variables that correlate with radiographic progression.
METHODS: Radiographs of the hands and feet were performed at baseline and at the end of study or early exit in 3 randomized controlled trials. Protocol US301 was a 12-month controlled trial of LEF or MTX treatment compared with placebo in 482 ...
Known for Radiographic Progression | Lef Mtx | Rheumatoid Arthritis | Randomized Controlled | 12 Months |
OBJECTIVE: RANKL is essential for osteoclast development, activation, and survival. Denosumab is a fully human monoclonal IgG2 antibody that binds RANKL, inhibiting its activity. The aim of this multicenter, randomized, double-blind, placebo-controlled, phase II study was to evaluate the effects of denosumab on structural damage in patients with rheumatoid arthritis (RA) receiving methotrexate treatment.
METHODS: RA patients received subcutaneous placebo (n = 75), denosumab 60 mg (n = ...
Known for Structural Damage | Bone Turnover | Rheumatoid Arthritis | Placebo Denosumab | Monoclonal Antibodies |
Etanercept treatment of psoriatic arthritis: Safety, efficacy, and effect on disease progression
[ PUBLICATION ]
OBJECTIVE: Etanercept has been shown to improve the articular and cutaneous manifestations of psoriatic arthritis (PsA). In this study, we further evaluated the safety, efficacy, and effect on radiographic progression of etanercept in patients with PsA.
METHODS: Patients with PsA (n = 205) were randomized to receive placebo or 25 mg etanercept subcutaneously twice weekly for 24 weeks. Patients continued to receive blind-labeled therapy in a maintenance phase until all had completed the ...
Known for Etanercept Treatment | Psoriatic Arthritis | 24 Weeks | Efficacy Safety | Placebo Patients |
OBJECTIVE: To evaluate the long-term effectiveness and tolerability of adalimumab in the treatment of psoriatic arthritis (PsA).
METHODS: Patients with PsA who completed a 24-week, double-blind study of adalimumab versus placebo were eligible to enroll in an open-label extension study and receive adalimumab 40 mg subcutaneously every other week for up to an additional 120 weeks. At the time of this analysis, available efficacy evaluations throughout 2 years of treatment (n = 245) ...
Known for Psoriatic Arthritis | Adalimumab Treatment | Monoclonal Antibodies | Patients Psa | Joint Disease |
OBJECTIVE: Joint damage is related to disease activity in rheumatoid arthritis (RA), but the degree of its progression and the temporal associations between disease activity and joint damage are unclear. The aim of this study was to evaluate whether there is a latency in the effect of disease activity on radiographic progression in patients with RA.
METHODS: Data were obtained from the PREMIER trial, a 2-year randomized, controlled clinical trial of adalimumab plus methotrexate versus ...
Known for Radiographic Progression | Sustained Remission | Rheumatoid Arthritis | Monoclonal Antibodies | Year Patients |
OBJECTIVE: To evaluate published proposed definitions of minimal disease activity (MDA) and remission in patients with early rheumatoid arthritis (RA).
METHODS: The cohort comprised disease-modifying antirheumatic drug (DMARD)-naive patients with early seropositive active RA (n = 200) treated with traditional DMARDs in the prebiologic era. MDA definitions included Disease Activity Score in 28 joints (DAS28) Known for Minimal Disease Activity | Arthritis Cohort | Mda Das28 | Remission Patients | Illness Terminology
OBJECTIVE: This study was conducted 1) to determine the feasibility of using computer programs to measure radiographic joint space width and estimate erosion volume in the hands of patients with rheumatoid arthritis (RA), and 2) to compare the new computer-based methods with established scoring methods.
METHODS: To measure the joint space width in the finger and wrist joints of RA patients, hand and wrist radiographic films were scanned using a tabletop scanner and analyzed with programs ...
Known for Erosion Volume | Joint Space | Rheumatoid Arthritis | Scoring Methods | Computer Assisted |