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Author/Creator Warner, Barbara B.

2. Antibiotic-driven intestinal dysbiosis in pediatric short bowel syndrome is associated with persistently altered microbiome functions and gut-derived bloodstream infections. (1st January 2021)

Authors:
Thänert, Robert; Thänert, Anna; Ou, Jocelyn; Bajinting, Adam; Burnham, Carey-Ann D.; Engelstad, Holly J.; Tecos, Maria E.; Ndao, I. Malick; Hall-Moore, Carla; Rouggly-Nickless, Colleen; Carl, Mike A.; Rubin, Deborah C.; Davidson, Nicholas O.; Tarr, Phillip I.; Warner, Barbara B.; Dantas, Gautam; ...
Journal:
Gut microbes
Issue:
Volume 13:Isuse 1(2021)
Page Start:
Record Type:
Journal Article
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4. Care Levels for Fetal Therapy Centers. Issue 6 (2nd June 2022)

Authors:
Baschat, Ahmet A.; Blackwell, Sean B.; Chatterjee, Debnath; Cummings, James J.; Emery, Stephen P.; Hirose, Shinjiro; Hollier, Lisa M.; Johnson, Anthony; Kilpatrick, Sarah J.; Luks, Francois I.; Menard, M. Kathryn; McCullough, Lawrence B.; Moldenhauer, Julie S.; Moon-Grady, Anita J.; Mychaliska, G...
Journal:
Obstetrics and gynecology
Issue:
Volume 139:Issue 6(2022)
Page Start:
1027
Record Type:
Journal Article
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6. Impact of Neonatal Intensive Care Bed Configuration on Rates of Late-Onset Bacterial Sepsis and Methicillin-Resistant Staphylococcus aureus Colonization. (25th June 2015)

Authors:
Julian, Samuel; Burnham, Carey-Ann D.; Sellenriek, Patricia; Shannon, William D.; Hamvas, Aaron; Tarr, Phillip I.; Warner, Barbara B.
Journal:
Infection control and hospital epidemiology
Issue:
Volume 36:Number 10(2015)
Page Start:
1173
Record Type:
Journal Article
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10. Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN). Issue 11 (17th August 2017)

Authors:
Wambach, Jennifer A.; Stettner, Georg M.; Haack, Tobias B.; Writzl, Karin; Škofljanec, Andreja; Maver, Aleš; Munell, Francina; Ossowski, Stephan; Bosio, Mattia; Wegner, Daniel J.; Shinawi, Marwan; Baldridge, Dustin; Alhaddad, Bader; Strom, Tim M.; Grange, Dorothy K.; Wilichowski, Ekkehard; Troxel...
Journal:
Human mutation
Issue:
Volume 38:Issue 11(2017)
Page Start:
1477
Record Type:
Journal Article
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