Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Theresa Wampler"'
Autor:
Leanne M. Mansfield, Sivia K. Lapidus, Samira Nazzar Romero, Lakshmi N. Moorthy, Felice C. Adler-Shohet, Matthew Hollander, Julie Cherian, Marinka Twilt, Geraldina Lionetti, Smriti Mohan, Patricia A. DeLaMora, Karen L. Durrant, Theresa Wampler Muskardin, Mariana Correia Marques, Karen B. Onel, Fatma Dedeoglu, Maria J. Gutierrez, Grant Schulert, the CARRA Autoinflammatory Network Consortium for the CARRA PFAPA/Autoinflammatory Working Group
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/8c2beb3253504e69afcf3364e66e6250
Autor:
Leanne M. Mansfield, Sivia K. Lapidus, Samira Nazzar Romero, Lakshmi N. Moorthy, Felice C. Adler-Shohet, Matthew Hollander, Julie Cherian, Marinka Twilt, Geraldina Lionetti, Smriti Mohan, Patricia A. DeLaMora, Karen L. Durrant, Theresa Wampler Muskardin, Mariana Correia Marques, Karen B. Onel, Fatma Dedeoglu, Maria J. Gutierrez, Grant Schulert, the CARRA Autoinflammatory Network Consortium for the CARRA PFAPA/Autoinflammatory Working Group, Shoghik Akoghlanian, Cassyanne L. Aguiar, Matthew Basiaga, Joyce Hui-Yuen, Elizabeth A. Kessler, Jamie Lai, Brian E. Nolan, Sheila Nolan, Melissa S. Oliver, Heather O Tory, Sirada Panupattanapong, Maryam Piram, Ann Szymanski, Tiphanie Vogel, Eveline Wu
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
The impact of the COVID-19 pandemic on new diagnoses of recurrent fevers and autoinflammatory diseases is largely unknown. The Childhood Arthritis and Rheumatology Research Alliance (CARRA) PFAPA/AID Working Group aimed to investigate the impact of t
Externí odkaz:
https://doaj.org/article/d9253a5419394c93882710b598d05dc8
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 4, Pp e278-e281 (2018)
ABSTRACT: Objective: To report a case of symptomatic vitamin D-mediated hypercalcemia in a girl with Blau syndrome, a rare granulomatous inflammatory disease occurring in early childhood. Methods: Clinical, laboratory, imaging, and genetic findings a
Externí odkaz:
https://doaj.org/article/3ac12460289745258d3fd10773ecf685
Autor:
Theresa Wampler Muskardin, Zhongbo Jin, Jessica M. Dorschner, Yogita Ghodke-Puranik, Timothy Niewold
Publikováno v:
Journal of Clinical and Translational Science, Vol 3, Pp 8-9 (2019)
OBJECTIVES/SPECIFIC AIMS: The cellular mechanisms that underlie the IFNβ/α ratio that predicts response are not known. Effects of IFN on single immune cells may be masked in whole blood or mixed cell populations. By studying the effect of IFNβ/α
Externí odkaz:
https://doaj.org/article/a2713f8136b949be848411cb630b5657
Publikováno v:
In AACE Clinical Case Reports July-August 2018 4(4):e278-e281
Autor:
Krause, Megan L., Zamora-Legoff, Jorge A., Crowson, Cynthia S., Muskardin, Theresa Wampler, Mason, Thomas, Matteson, Eric L.
Publikováno v:
In Seminars in Arthritis and Rheumatism February 2017 46(4):439-443
Akademický článek
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Autor:
Lauren S. Schaefer, Theresa Wampler Muskardin, Jan‐Mendelt Tillema, Carilyn Wieland, Megha M. Tollefson
Publikováno v:
Pediatric Dermatology. 39:112-114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c341a83b701d127faa73d2568bdd2bfe
https://doi.org/10.1111/pde.14878
https://doi.org/10.1111/pde.14878
Autor:
Joao Bosco Oliveira, Amanda Virginia Cavalcante, Catherine Castro, Timothy B. Niewold, Simone Appenzeller, Luciana B Paim-Marques, Theresa Wampler Muskardin
Publikováno v:
Rheumatology International. 41:219-225
Cryopyrin-associated periodic syndromes (CAPS) are a group of autoinflammatory diseases associated with NLRP3 gain of function mutations. CAPS associated mutations are found predominantly in exon 3. The objective of this study is to describe a new va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7a1f6326dac6d43ba6e9e08cd46b147
https://doi.org/10.1007/s00296-020-04683-5
https://doi.org/10.1007/s00296-020-04683-5
Publikováno v:
Mult Scler
Systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) are two common autoimmune rheumatic diseases that vary in severity, clinical presentation, and disease course between individuals. Molecular and genetic studies of both diseases have id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdc63ce0950e41e21277cbc294560570
https://doi.org/10.1177/1352458519884249
https://doi.org/10.1177/1352458519884249