Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E. Legger"'
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Autoinflammatory diseases are rare disorders of the innate immune system characterized by fever and other signs of inflammation. A feared complication of autoinflammatory diseases is the development of AA amyloidosis. AA amyloidos
Externí odkaz:
https://doaj.org/article/580038b4b5fb46d6841240b46319a593
Autor:
Marc H A Jansen, Christien Rondaan, Geertje E Legger, Kirsten Minden, Yosef Uziel, Natasa Toplak, Despoina Maritsi, Lotte van den Berg, Guy A M Berbers, Patricia Bruijning, Yona Egert, Christophe Normand, Marc Bijl, Helen E Foster, Isabelle Koné-Paut, Carine Wouters, Angelo Ravelli, Ori Elkayam, Nicolaas M Wulffraat, Marloes W Heijstek
Publikováno v:
Annals of the Rheumatic Diseases, 82, 35-47. BMJ PUBLISHING GROUP
ObjectivesRecent insights supporting the safety of live-attenuated vaccines and novel studies on the immunogenicity of vaccinations in the era of biological disease-modifying antirheumatic drugs in paediatric patients with autoimmune/inflammatory rhe
Autor:
Geertje E, Legger, Margit B, Erdtsieck, Liseth, de Wolff, Alja J, Stel, Leonoor I, Los, Gwenny M, Verstappen, Fred K L, Spijkervet, Arjan, Vissink, Bert, van der Vegt, Frans G M, Kroese, Wineke, Armbrust, Suzanne, Arends, Hendrika, Bootsma
Publikováno v:
Clinical and Experimental Rheumatology. 39:85-92
Primary Sjögren's syndrome (pSS) is a rare disease in paediatric patients. Presenting symptoms differ from those in adult patients. The aim of this study was to evaluate presenting symptoms, classification criteria and clinical assessments, includin
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Autor:
Salah Ali, Yenan T. Bryceson, Marina Garcia-Prat, Maximilian Heeg, Jeffrey J. Bednarski, Carsten Speckmann, Jelena Rascon, Viktorija Kenina, Annaliesse Blincoe, Melissa Hines, Rebecca A. Marsh, Elie Haddad, Julie-An Talano, Anne Lortie, Patrick Campbell, Natalja Kurjane, Geertje E. Legger, Amer Khojah, Fabien Touzot, yasmine El Chazli, Julia T. Warren, Erica G. Schmitt, Marisa Klein-Gitelman, Stephan Ehl, Laura C. Alonso, Austen Worth, Maria C. Putti, Joerg Krueger, Evangeline Wassmer, Jacques G. Rivière, Kai Lehmberg, Itziar Astigarraga, Gal Goldstein, Kuang-Yueh Chiang, Inita Bulina, Claire Booth, Arjan C. Lankester, Michael M. Henry, Sarah Maier, Marwa Abd El-Maksoud, Steven M. Holland
Publikováno v:
Journal of Clinical Immunology, 40(6), 901-916. SPRINGER/PLENUM PUBLISHERS
Isolated neuroinflammatory disease has been described in case reports of familial hemophagocytic lymphohistiocytosis (FHL), but the clinical spectrum of disease manifestations, response to therapy and prognosis remain poorly defined. We combined an i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::935190329c47a2ed45210a2243c64f4a
https://hdl.handle.net/1887/3181390
https://hdl.handle.net/1887/3181390
Autor:
S. Cederholm, Nicolino Ruperto, Paul A. Brogan, D. Lindqvist, H Lachmann, Francesca Bagnasco, Marco Gattorno, Gabriella Giancane, E. Legger, Riccardo Papa
Publikováno v:
Annals of the Rheumatic Diseases. 80:947.2-948
Background:Cryopyrin associated periodic syndromes (CAPS) are a group of ultra-rare autoinflammatory diseases caused by mutations in the NLRP3 gene, leading to overproduction of IL-1β. CAPS includes the following subdiagnoses: familial cold autoinfl
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(17)
A 13-year-old girl presented with rectal bleeding, abdominal pain and a palpable mass in the lower right abdomen. The history mentioned a chronic anaemia since she was 2 years old. Further examination did not give any indications for inflammation as
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