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Lupus|July 31, 2019
Complex medical history of a patient with a compound heterozygous mutation in C1QCR Lubbers, L J J Beaart-van de Voorde, K van Leeuwen, et al.
Human Immunology|December 29, 2004
Expression of FOXP3 mRNA is not confined to CD4+CD25+ T regulatory cells in humansMary E Morgan, Jolanda H M van Bilsen, Aleida M Bakker, et al.
Annals of the Rheumatic Diseases|March 10, 2012
Remission induction therapy with methotrexate and prednisone in patients with early rheumatoid and undifferentiated arthritis (the IMPROVED study)Kirsten Wevers-de Boer, Karen Visser, Lotte Heimans, et al.
Annals of the Rheumatic Diseases|May 23, 2013
A genetic variant in the region of MMP-9 is associated with serum levels and progression of joint damage in rheumatoid arthritisD P C de Rooy, A Zhernakova, R Tsonaka, et al.
Journal of Scleroderma and Related Disorders|February 6, 2023
Mouth opening in systemic sclerosis: Its course over time, determinants and impact on mouth handicapSarah J H Khidir, Maaike Boonstra, Sytske Anne Bergstra, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 27, 2021
Anticentromere Antibody Levels and Isotypes and the Development of Systemic SclerosisNina M van Leeuwen, Maaike Boonstra, Jaap A Bakker, et al.
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