Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rachel S Tattersall"'
Publikováno v:
Clinical Infection in Practice, Vol 12, Iss , Pp 100092- (2021)
Background: Multisystem Inflammatory Syndrome in Adults (MIS-A) is a recently emerging condition that occurs as a delayed complication of COVID-19 infection. It involves inflammation of multiple extra-pulmonary organ systems. Diagnostic criteria and
Externí odkaz:
https://doaj.org/article/568a8b495d4948a5911c2e9ffc3b73c9
Autor:
Neal S Shah, Matthew Hutchinson, Samuel Clark, Emilie Sanchez, Michael Brown, Neil Stone, Aisling S Carr, Ben Carpenter, Arian Laurence, Satyen H Gohil, Rachel S Tattersall, Jessica J Manson, Alexis Jones
Publikováno v:
Rheumatology. 62
Background/Aims Haemophagocytic lymphohistiocytosis (HLH) is a devastating condition caused by uncontrolled activation of the immune system. If left untreated, the condition leads to multi-organ failure and death. Even with treatment, recent UK data
Publikováno v:
Rheumatology. 62
Background/Aims Haemophagocytic lymphocytosis (HLH) is a multi-system hyperinflammatory syndrome with high mortality. Early treatment and multi-disciplinary team (MDT) management improves outcomes. In 2021, NHS England released guidelines for HLH tre
Autor:
Marcela A. Ferrada, Sinisa Savic, Daniela Ospina Cardona, Jason C. Collins, Hugh Alessi, Fernanda Gutierrez-Rodrigues, Dinesh Babu Uthaya Kumar, Lorena Wilson, Wendy Goodspeed, James S. Topilow, Julie J. Paik, James A. Poulter, Tanaz A. Kermani, Matthew J. Koster, Kenneth J. Warrington, Catherine Cargo, Rachel S. Tattersall, Christopher J. A. Duncan, Anna Cantor, Patrycja Hoffmann, Elspeth M. Payne, Hanna Bonnekoh, Karoline Krause, Edward W. Cowen, Katherine R. Calvo, Bhavisha A. Patel, Amanda K. Ombrello, Daniel L. Kastner, Neal S. Young, Achim Werner, Peter C. Grayson, David B. Beck
Somatic mutations in UBA1 cause vacuoles, E1 ubiquitin-activating enzyme, X-linked, autoinflammatory somatic (VEXAS) syndrome, an adult-onset inflammatory disease with an overlap of hematologic manifestations. VEXAS syndrome is characterized by a hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af8c674df36e5d2fbb8743262ff01d7b
https://eprints.whiterose.ac.uk/191042/1/106414_1_merged_1656075092.pdf
https://eprints.whiterose.ac.uk/191042/1/106414_1_merged_1656075092.pdf
Autor:
Varvara Choida, Rachel S Tattersall, Jessica J Manson, Debajit Sen, Coziana Ciurtin, Margaret A Hall-Craggs
Publikováno v:
Rheumatology. 61
Background/Aims To assess the potential for whole-body MRI (WBMRI) to modify rheumatologists’ impression of disease activity and treatment management in adolescent patients with JIA. Methods Two rheumatology consultants experienced in managing peop
Autor:
Joe West, Tim R. Card, Mark J. Bishton, Peter Lanyon, Lu Ban, Mary Bythell, Lucy Elliss‐Brookes, Jessica J. Manson, Vasanta Nanduri, Judith Rankin, Rachel S. Tattersall, Colin J. Crooks
Publikováno v:
Journal of internal medicineReferences. 291(4)
Background: Haemophagocytic lymphohistiocytosis (HLH) is a rare hyper-inflammatory condition with poor outcomes. Objectives: Few population-based estimates of the incidence and survival in adults exist. We aimed to provide these data for England. Met
This concise guide takes a practical approach to adolescent and young adult (AYA) rheumatology, aiming to cover the needs of any healthcare professional dealing with young people aged 10-24 years. Each chapter contains key management points for read