Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jacoba Carolien Graver"'
Autor:
Valérie Devauchelle-Pensec, Jacoba Carolien Graver, Yannick van Sleen, Elisabeth Brouwer, Divi Cornec, Guillermo Carvajal Alegria, Maria Sandovici
Publikováno v:
Revue du Rhumatisme. 88:405-409
Autor:
Annemieke M. H. Boots, Elisabeth Brouwer, Wayel H. Abdulahad, Jacoba Carolien Graver, Maria Sandovici, Kornelis S M van der Geest, Peter Heeringa
Publikováno v:
Journal of Autoimmunity, 123:102684. ACADEMIC PRESS LTD-ELSEVIER SCIENCE LTD
OBJECTIVE: B-cells are present in the inflamed arteries of giant cell arteritis (GCA) patients and a disturbed B-cell homeostasis is reported in peripheral blood of both GCA and the overlapping disease polymyalgia rheumatica (PMR). In this study, we
Autor:
Guillermo Carvajal Alegria, Divi Cornec, Maria Sandovici, Jacoba Carolien Graver, Yannick van Sleen, Valérie Devauchelle-Pensec, Elisabeth Brouwer
Publikováno v:
Joint bone spine, 88(2):105045. ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Autor:
Maria Sandovici, Elisabeth Brouwer, Wayel H. Abdulahad, Peter Heeringa, A. Boots, D. Altulea, Jacoba Carolien Graver, William F Jiemy
Publikováno v:
Annals of the Rheumatic Diseases. 80:33.1-34
Background:Giant cell arteritis (GCA) is the most frequent form of systemic vasculitis affecting the temporal artery (TA) and the aorta. Macrophages and T cells are well recognized players in the pathogenesis of GCA while B cells are often not taken
Autor:
Jacoba Carolien Graver, Elisabeth Brouwer, Yannick van Sleen, Annemieke M. H. Boots, Wayel H. Abdulahad, Maria Sandovici, Kornelis S M van der Geest
Publikováno v:
Frontiers in Immunology, 10:1981. Frontiers Media SA
Frontiers in Immunology
Frontiers in Immunology, Vol 10 (2019)
Frontiers in Immunology
Frontiers in Immunology, Vol 10 (2019)
Giant cell arteritis (GCA) and polymyalgia rheumatica (PMR) are inflammatory diseases requiring long-term glucocorticoid treatment. Limited data on dynamics in leukocyte counts before, during and after treatment are available. Leukocyte counts were m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22f4ee386af05f5e99cc2efd5935861
https://research.rug.nl/en/publications/2a140217-0dea-4d7e-96e2-2bcb4c2d3132
https://research.rug.nl/en/publications/2a140217-0dea-4d7e-96e2-2bcb4c2d3132
Autor:
Kornelis S M van der Geest, Annemieke M. H. Boots, Jacoba Carolien Graver, Yannick van Sleen, Wayel H. Abdulahad, Elisabeth Brouwer, Maria Sandovici
Publikováno v:
Saturday, 15 June 2019.
Background: Giant cell arteritis (GCA) and polymyalgia rheumatica (PMR) are inflammatory diseases requiring long-term treatment with glucocorticoids. Currently, only limited data on dynamics of peripheral leukocytes and leukocyte subset composition b
Autor:
Maria Sandovici, Yannick van Sleen, Elisabeth Brouwer, Jacoba Carolien Graver, Kornelis S M van der Geest, Wayel Abdullahad, Annemieke M. H. Boots
Publikováno v:
Rheumatology. 58
Autor:
Elisabeth Brouwer, Johan Bijzet, D. Wolbers, Annemieke M. H. Boots, Maria Sandovici, Wayel H. Abdulahad, Jacoba Carolien Graver
Publikováno v:
Annals of the Rheumatic Diseases. 79:234.2-234
Background:The presence of organised B cells in both cranial-giant cell arteritis (C-GCA) (temporal artery) and large vessel (LV)-GCA (aorta) has previously been documented. The number and the extent of organisation of B cells in tertiary lymphoid or
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background Giant cell arteritis (GCA) is the most common type of systemic vasculitis. Currently, two forms of GCA are described: a cranial(C)-GCA and a systemic, large-vessel (LV)-GCA. LV-GCA frequently occurs without specific symptoms and late compl
Autor:
Annemieke M. H. Boots, Maria Sandovici, Jacoba Carolien Graver, Arjan Diepstra, Elisabeth Brouwer
Publikováno v:
Annals of the Rheumatic Diseases, 77(3):16. BMJ PUBLISHING GROUP
With great interest, we read the article by Ciccia et al, about artery tertiary lymphoid organs (ATLOs) in giant cell arteritis (GCA) and the association with ectopic expression of constitutive lymphoid tissue-homing chemokines.1 In 50 patients with