Zobrazeno 1 - 10
of 813
pro vyhledávání: '"PERIODIC FEVER SYNDROME"'
Autor:
Yuri Hayashida, Maho Hatano, Kazuyuki Ito, Manabu Sugie, Junko Kunieda, Masaki Shimizu, Tomohiro Morio, Chikako Morioka
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Cryopyrin-associated periodic syndrome (CAPS) is a genetic disorder and autoinflammatory disease characterized by chronic inflammation throughout the body. The most severe form of CAPS, Chronic Infantile Neurologic Cutaneous, and Articular (CINCA) sy
Externí odkaz:
https://doaj.org/article/384dbb8f304449f6967bbb66dc1733c7
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Systemic autoinflammatory diseases (SAIDs) are a group of rare diseases characterized by recurrent or continuous inflammation, typically accompanied by genetic variants. Good responses to anti-TNF therapy were observed in SAIDs patients. However, the
Externí odkaz:
https://doaj.org/article/b77b10705b384ab395f25be608952d85
Autor:
Peter Hur, Kathleen G. Lomax, Raluca Ionescu-Ittu, Ameur M. Manceur, Jipan Xie, Jordan Cammarota, Raju Gautam, Navneet Sanghera, Nina Kim, Alexei A. Grom
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-13 (2021)
Abstract Background Although canakinumab has demonstrated efficacy in multiple trials in patients with periodic fever syndromes (PFS), the evidence on initiation of canakinumab among PFS patients in real world setting is not well understood. We aimed
Externí odkaz:
https://doaj.org/article/895a29c829b840f387ab20d693d70cfe
Autor:
Kari Hemminki, Asta Försti
Publikováno v:
Hemato, Vol 2, Iss 3, Pp 429-440 (2021)
We reviewed our studies on epidemiology and germline genetics of amyloidosis. In epidemiology, we considered both hereditary and non-hereditary amyloidosis. As the source of data, we used the nationwide Swedish hospital discharge register. We estimat
Externí odkaz:
https://doaj.org/article/7922cb0a6ce24b1fa8e7adf69e3d97a8
Autor:
Hari Kishan Boorugu, Rajendra Vara Prasad Irlapati, Pankaj Vinod Jariwala, Kartik Pandurang Jadhav
Publikováno v:
Current Medical Issues, Vol 20, Iss 2, Pp 104-106 (2022)
Hereditary recurrent fever syndromes are rarely diagnosed in India, and the age at diagnosis is usually childhood or early adulthood. We present an adult male patient with recurrent fever since childhood who presented to us at 59 years of age and was
Externí odkaz:
https://doaj.org/article/39d5b21854f44da5968b800fbe6a679a
Autor:
Najla Aljaberi, Elena Tronconi, Grant Schulert, Alexei A. Grom, Daniel J. Lovell, Jennifer L. Huggins, Michael Henrickson, Hermine I. Brunner
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 18, Iss 1, Pp 1-6 (2020)
Abstract Background Serum phagocyte-derived alarmins S100A8/9 and S100A12 are considered useful for the assessment of inflammatory diseases. Our study evaluated the use of S100 proteins in a pediatric clinical setting for estimating disease activity
Externí odkaz:
https://doaj.org/article/64aab2d1a7854ac6b6bca21c0423981f
Autor:
Lori B. Tucker, Lovro Lamot, Iwona Niemietz, Brian K. Chung, David A. Cabral, Kristin Houghton, Ross E. Petty, Kimberly A. Morishita, Gillian I. Rice, Stuart E. Turvey, William T. Gibson, Kelly L. Brown
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 17, Iss 1, Pp 1-7 (2019)
Abstract Background Despite recent advances in the diagnosis and understanding of many autoinflammatory diseases, there are still a great number of patients with phenotypes that do not fit any clinically- and/or genetically-defined disorders. Case pr
Externí odkaz:
https://doaj.org/article/6242ac0750c34aabb76f48ca9a2c8b8b
Autor:
Tiziana Coppola, Bradford Becken, Heather Van Mater, Marie Theresa McDonald, Gabriela Maradiaga Panayotti
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background This case follows a 14-month-old female, who despite multiple presentations to several physicians, continued to have recurrent febrile episodes with gross motor delay. Her case revealed an often missed diagnosis of Mevalonate Kina
Externí odkaz:
https://doaj.org/article/b5e52bec47f04c709af3c30a65d1cbfe
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