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Stanisław Sierakowski

Researcher at Medical University of Białystok

Publications -  128
Citations -  3367

Stanisław Sierakowski is an academic researcher from Medical University of Białystok. The author has contributed to research in topics: Rheumatoid arthritis & Arthritis. The author has an hindex of 32, co-authored 128 publications receiving 3106 citations.

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Efficacy of modified-release versus standard prednisone to reduce duration of morning stiffness of the joints in rheumatoid arthritis (CAPRA-1): a double-blind, randomised controlled trial

TL;DR: Modified-release prednisone is well tolerated, convenient to administer, and produces a clinically relevant reduction of morning stiffness of the joints in addition to all known therapeutic effects of immediate-releaseprednisone.
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Work disability remains a major problem in rheumatoid arthritis in the 2000s: data from 32 countries in the QUEST-RA Study

TL;DR: The Quantitative Standard Monitoring of Patients with RA (QUEST-RA) multinational database of 8,039 patients in 86 sites in 32 countries, 16 with high gross domestic product (GDP) and 16 low-GDP countries, analyzed for work and disability status at onset and over the course of RA and clinical status of patients who continued working or had stopped working according to all RA Core Data Set measures.
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QUEST-RA: Quantitative clinical assessment of patients with rheumatoid arthritis seen in standard rheumatology care in 15 countries

TL;DR: This international multicentre cross-sectional database provides an overview of clinical status and treatments of patients with RA in standard clinical care in 2005–6 including countries that are infrequently involved in clinical research projects.
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Soluble adhesion molecules (ICAM-1, VCAM-1, and E-selectin) and vascular endothelial growth factor (VEGF) in patients with distinct variants of rheumatoid synovitis

TL;DR: The distinct histological appearances of rheumatoid synovitis associated with different serum profiles of sICAM-1, sVCAM- 1, and VEGF reflect varied clinical activity of the disease and confirm RA heterogeneity.