Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Tiphanie P, Vogel"'
Autor:
Stephanie Wood, Justin Branch, Priscilla Vasquez, Marietta M. DeGuzman, Amanda Brown, Anna Carmela Sagcal-Gironella, Saimun Singla, Andrea Ramirez, Tiphanie P. Vogel
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-11 (2024)
Abstract Background A better understanding of the pathogenesis of polyarticular juvenile idiopathic arthritis (polyJIA) is needed to aide in the development of data-driven approaches to guide selection between therapeutic options. One inflammatory pa
Externí odkaz:
https://doaj.org/article/e561e45c25344ecc838810ae86e2df58
Autor:
Alejandro Nieto-Patlán, Natalia S. Fernández Dávila, Yuqing Wang, Michelle Zelnick, Eyal Muscal, Martha Curry, James R. Lupski, Steven M. Holland, Bo Yuan, Douglas B. Kuhns, Tiphanie P. Vogel, Ivan K. Chinn
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionSystemic lupus erythematosus is a multi-faceted autoimmune disorder of complex etiology. Pre-pubertal onset of pediatric systemic lupus erythematosus (pSLE) is uncommon and should raise suspicion for a genetic driver of disease. Autosomal
Externí odkaz:
https://doaj.org/article/5926a4b411d84bacae707c1d876e5f92
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
STAT3 gain-of-function (GOF) syndrome is a multi-organ primary immune regulatory disorder characterized by early onset autoimmunity. Patients present early in life, most commonly with lymphoproliferation, autoimmune cytopenias, and growth delay. Howe
Externí odkaz:
https://doaj.org/article/902795234b104a8994c3da97f3fada3a
Autor:
Erica G. Schmitt, Kelsey A. Toth, Samuel I. Risma, Ana Kolicheski, Nermina Saucier, Rafael J. Feliciano Berríos, Zev J. Greenberg, Jennifer W. Leiding, Jack J. Bleesing, Akaluck Thatayatikom, Laura G. Schuettpelz, John R. Edwards, Tiphanie P. Vogel, Megan A. Cooper
Publikováno v:
JCI Insight, Vol 7, Iss 21 (2022)
Primary immune regulatory disorders (PIRD) represent a group of disorders characterized by immune dysregulation, presenting with a wide range of clinical disease, including autoimmunity, autoinflammation, or lymphoproliferation. Autosomal dominant ge
Externí odkaz:
https://doaj.org/article/d12a4668e30f4d379c2f85598786cc63
Autor:
Prasanna Venkatesh Ramachandran, C. Mary Healy, Elton M. Lambert, Deyanara Guerra, Choladda V. Curry, Tiphanie P. Vogel
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Elevated immunoglobulin E (IgE) levels can be associated with infectious, allergic and inflammatory disorders, and rarely as a manifestation of an inborn error of immunity. Here we report the case of an adolescent female who presented with a graduall
Externí odkaz:
https://doaj.org/article/7c077358d0064b83aac11705f1e5cb44
Autor:
Josefina Longeri Contreras, Mabel A. Ladino, Katherine Aránguiz, Gonzalo P. Mendez, Zeynep Coban-Akdemir, Bo Yuan, Richard A. Gibbs, Lindsay C. Burrage, James R. Lupski, Ivan K. Chinn, Tiphanie P. Vogel, Jordan S. Orange, M. Cecilia Poli
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Lysinuric protein intolerance (LPI) is an inborn error of metabolism caused by defective transport of cationic amino acids in epithelial cells of intestines, kidneys and other tissues as well as non-epithelial cells including macrophages. LPI is caus
Externí odkaz:
https://doaj.org/article/7f674538bee04d729f9bb565e0c6aa14
Autor:
HaiThuy N. Nguyen, Rida Salman, Tiphanie P. Vogel, Manuel Silva-Carmona, Marietta DeGuzman, R. Paul Guillerman
Publikováno v:
Pediatric Radiology. 53:844-853
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c44bde2c5a34b69635b5a3ce0233664
https://doi.org/10.1007/s00247-023-05600-1
https://doi.org/10.1007/s00247-023-05600-1
Autor:
Bahar K. Force, Tiphanie P. Vogel, Dang M. Nguyen, Kent A. Heck, Sherly Sebastian, Mas Takashima, Daniel Yoshor, Susan L. Samson
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Background: Hypophysitis is primary or idiopathic or secondary to another disease process. The histologic subtypes of hypophysitis are lymphocytic, granulomatous, xanthomatous, xanthogranulomatous, or IgG4-related. Granulomatous hypophysitis is the s
Externí odkaz:
https://doaj.org/article/191bda5723dc4f99a6d2135758fad685
Autor:
Yike Jiang, Mihail Firan, Sarada L. Nandiwada, Anaid Reyes, Rebecca A. Marsh, Tiphanie P. Vogel, Joud Hajjar
Publikováno v:
Case Reports in Immunology, Vol 2020 (2020)
X-linked lymphoproliferative disease (XLP1) is a rare primary immunodeficiency characterized by EBV-triggered immune dysregulation, lymphoproliferation, dysgammaglobulinemia, and lymphoma. Early childhood mortality from overwhelming inflammation is e
Externí odkaz:
https://doaj.org/article/75d608f4b3514744aae87f2e0f0e2b73
Autor:
Natalia S. Chaimowitz, Justin Branch, Anaid Reyes, Alexander Vargas-Hernández, Jordan S. Orange, Lisa R. Forbes, Mohammed Ehlayel, Saleema C. Purayil, Maryam Ali Al-Nesf, Tiphanie P. Vogel
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Autosomal dominant hyper-IgE syndrome caused by mutations in the transcription factor STAT3 (AD-HIES) is characterized by a collection of immunologic and non-immune features including eczema, recurrent infections, elevated IgE levels, and connective
Externí odkaz:
https://doaj.org/article/636fc4e955c54f929bec846ffd1f8034