Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elizabeth Mannino Avila"'
Autor:
Sarah Gray, Begem Lee, Michael Levy, Tiranun Rungvivatjarus, Aarti Patel, Elizabeth Mannino Avila, Erin Fisher, Kyung E. Rhee
Publikováno v:
Hospital Pediatrics. 13:159-167
OBJECTIVE Oral feeding by children with bronchiolitis on high-flow nasal cannula (HFNC) is questioned, resulting in high practice variability. Our objective was to determine the incidence of aspiration pneumonia and adverse feeding events in otherwis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b5dcebc87989efdd1da7edd302de89e
https://doi.org/10.1542/hpeds.2022-006740
https://doi.org/10.1542/hpeds.2022-006740
Publikováno v:
Pediatrics. 147:16-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a27c4fa8f59d409f6ac3938ce7b9876a
https://doi.org/10.1542/peds.147.3ma1.16
https://doi.org/10.1542/peds.147.3ma1.16
Publikováno v:
Pediatric emergency care. 37(6)
OBJECTIVE The objective of this study was to examine patient history as well as clinical and laboratory features associated with true bacteremia versus false bacteremia in previously healthy febrile children ages 0 to 36 months in the era of polyvale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a75c8f765be4ea13614779c43d38145
https://pubmed.ncbi.nlm.nih.gov/30106869
https://pubmed.ncbi.nlm.nih.gov/30106869
Autor:
Pamela Welch, Elizabeth Mannino Avila, Colleen Hadigan, Alexandra F. Freeman, Pamela A. Shaw, Joie Davis, Jatin R. Matta, Amy P. Hsu, Steven M. Holland, Ahmed M. Gharib, Roderic I. Pettigrew
Publikováno v:
Journal of Clinical Immunology. 31:338-345
Hyper-IgE syndrome (HIES) is a rare primary immunodeficiency caused by autosomal dominant STAT3 mutations resulting in recurrent infections and connective tissue abnormalities. Coronary artery abnormalities have been reported infrequently. We aimed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79181000d0c451e62c1e575ed271e971
https://doi.org/10.1007/s10875-011-9515-9
https://doi.org/10.1007/s10875-011-9515-9
Publikováno v:
Annals of Allergy, Asthma & Immunology. 115:157-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f7ffe1aefa6cac55e1af834a6f7f7f5
https://doi.org/10.1016/j.anai.2015.05.022
https://doi.org/10.1016/j.anai.2015.05.022
Autor:
Alexandra F. Freeman, Joshua D. Milner, Gulbu Uzel, Maria L. Turner, Elizabeth Mannino Avila, Steven M. Holland, Amy P. Hsu, Stefania Pittaluga
Publikováno v:
Pediatrics. 126(5)
Hypomorphic mutations that lead to “leaky” severe combined immunodeficiency presentation with partial protein function are increasingly being identified. Mutations in recombination-activating genes (RAGs) 1 and 2 cause immunodeficiency and dysreg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c064cc7a03541df3bfbb22a0b3cc3aa
https://pubmed.ncbi.nlm.nih.gov/20956421
https://pubmed.ncbi.nlm.nih.gov/20956421