Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Anna K. Meyer"'
Autor:
Ludmila Perelygina, Raeesa Faisthalab, Emily Abernathy, Min-hsin Chen, LiJuan Hao, Lionel Bercovitch, Diana K. Bayer, Lenora M. Noroski, Michael T. Lam, Maria Pia Cicalese, Waleed Al-Herz, Arti Nanda, Joud Hajjar, Koen Vanden Driessche, Shari Schroven, Julie Leysen, Misha Rosenbach, Philipp Peters, Johannes Raedler, Michael H. Albert, Roshini S. Abraham, Hemalatha G. Rangarjan, David Buchbinder, Lisa Kobrynski, Anne Pham-Huy, Julie Dhossche, Charlotte Cunningham Rundles, Anna K. Meyer, Amy Theos, T. Prescott Atkinson, Amy Musiek, Mehdi Adeli, Ute Derichs, Christoph Walz, Renate Krüger, Horst von Bernuth, Christoph Klein, Joseph Icenogle, Fabian Hauck, Kathleen E. Sullivan
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Rubella virus (RuV) has recently been found in association with granulomatous inflammation of the skin and several internal organs in patients with inborn errors of immunity (IEI). The cellular tropism and molecular mechanisms of RuV persistence and
Externí odkaz:
https://doaj.org/article/42a46da9868e480f8c8f79db28a8fb27
Autor:
Emma Westermann-Clark, Cristina Adelia Meehan, Anna K. Meyer, Joseph F. Dasso, Devendra Amre, Maryssa Ellison, Bhumika Patel, Marisol Betensky, Charles Isaac Hauk, Jennifer Mayer, Jonathan Metts, Jennifer W. Leiding, Panida Sriaroon, Ambuj Kumar, Irmel Ayala, Jolan E. Walter
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundPrimary immunodeficiency is common among patients with autoimmune cytopenia.ObjectiveThe purpose of this study is to retrospectively identify key clinical features and biomarkers of primary immunodeficiency (PID) in pediatric patients with
Externí odkaz:
https://doaj.org/article/4d1e3fa278d5481e970bc605a7c10d21
Autor:
Anna K. Meyer, Mindy Banks, Tibor Nadasdy, Jennifer J. Clark, Rui Zheng, Erwin W. Gelfand, Jordan K. Abbott
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
A subset of patients with Ataxia-Telangiectasia (A-T) have dramatically reduced levels of IgG, IgA, and IgE with retained or elevated IgM levels. Several reports suggest that these A-T patients with a “hyper-IgM phenotype” (HIgM) suffer more clin
Externí odkaz:
https://doaj.org/article/0c90d378b24c4ed6b75b7b79b325d3a3
Autor:
Pooja Purswani, Cristina Adelia Meehan, Hye Sun Kuehn, Yenhui Chang, Joseph F. Dasso, Anna K. Meyer, Boglarka Ujhazi, Krisztian Csomos, David Lindsay, Taylor Alberdi, Sonia Joychan, Jessica Trotter, Carla Duff, Maryssa Ellison, Jack Bleesing, Attila Kumanovics, Anne M. Comeau, Jaime E. Hale, Luigi D. Notarangelo, Troy R. Torgersen, Hans D. Ochs, Panida Sriaroon, Benjamin Oshrine, Aleksandra Petrovic, Sergio D. Rosenzweig, Jennifer W. Leiding, Jolan E. Walter
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
In the era of newborn screening (NBS) for severe combined immunodeficiency (SCID) and the possibility of gene therapy (GT), it is important to link SCID phenotype to the underlying genetic disease. In western countries, X-linked interleukin 2 recepto
Externí odkaz:
https://doaj.org/article/7dff6da8b9b04db68c6c1cd6a8c8dac3
Publikováno v:
The Laryngoscope. 132:2505-2512
Assess current frenotomy practice patterns of pediatric otolaryngologists via a cross-sectional survey.Survey study.A 31-question electronic survey assessing frenotomy practice patterns was distributed to all American Society of Pediatric Otolaryngol
Autor:
Molly Eiseman, Madeleine P. Strohl, Anna K. Meyer, Dylan K. Chan, Melissa Ho, C Sayard Benvenuti, Chiara Scarpelli, Michelle M Florentine
Publikováno v:
Otolaryngology–Head and Neck Surgery. 167:170-177
To evaluate the effect of demographic disparities on language outcomes in a diverse group of children who are deaf or hard of hearing.Retrospective cohort study.UCSF Benioff Children's Hospital (a tertiary care center).Forty-four patients aged18 year
Autor:
Lisa Satterfield, Jonathan Walsh, Jeffrey P. Simons, Seth R. Schwartz, Erin M. Lambie, Richard M. Rosenfeld, Stacey L. Ishman, Sanjay R. Parikh, Cristina M. Baldassari, Anna K. Meyer, Daniel L. Wohl, David H. Darrow, Jessica R. Levi, Anna H. Messner, Scott E. Brietzke, Nira A. Goldstein
Publikováno v:
Otolaryngology–Head and Neck Surgery. 162:597-611
To identify and seek consensus on issues and controversies related to ankyloglossia and upper lip tie in children by using established methodology for American Academy of Otolaryngology-Head and Neck Surgery clinical consensus statements.An expert pa
Autor:
Michelle M Florentine, Stephanie L Rouse, Jihyun Stephans, David Conrad, Josephine Czechowicz, Ian R Matthews, Anna K Meyer, Garani S Nadaraja, Rajan Parikh, Jordan Virbalas, Jacqueline E Weinstein, Dylan K Chan
Understanding racial/ethnic disparities in diagnostic rates of genetic testing is critical for health equity. We sought to understand the extent and cause of racial/ethnic disparities in diagnostic efficacy of comprehensive genetic testing (CGT) for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c17f84b3ec4e371251872f0618d48a6
https://doi.org/10.21203/rs.3.rs-482542/v1
https://doi.org/10.21203/rs.3.rs-482542/v1
Autor:
Jordan Virbalas, Josephine A. Czechowicz, Anna K. Meyer, Dylan K. Chan, Ian R. Matthews, Jacqueline E. Weinstein, Michelle M Florentine, David E. Conrad, Jihyun Stephans, Stephanie L Rouse, Garani S. Nadaraja, Rajan Parikh
Publikováno v:
Human genetics. 141(3-4)
Understanding racial and ethnic disparities in diagnostic rates of genetic testing is critical for health equity. We sought to understand the extent and cause of racial and ethnic disparities in diagnostic efficacy of comprehensive genetic testing (C
Genetic Testing Leading to Early Identification of Childhood Ocular Manifestations of Usher Syndrome
Autor:
Dylan K. Chan, Anthony T. Moore, Anna K. Meyer, Anne Slavotinek, Jacqueline E. Weinstein, David E. Conrad, Garani S. Nadaraja, Kara D Brodie
Publikováno v:
The LaryngoscopeREFERENCES. 131(6)
OBJECTIVES Hearing-loss gene panel testing (HLGPT) is increasingly accessible as a first-line test in determining the etiology of sensorineural hearing loss (SNHL) in children. A major advantage of HLGPT is early identification of syndromic forms of