Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kimberly M. Thornton"'
Publikováno v:
International Journal of Pediatrics, Vol 2014 (2014)
Objective. This retrospective cohort study evaluated the effects of whole body therapeutic hypothermia (WBTH) on gastrointestinal (GI) morbidity and feeding tolerance in infants with moderate-to-severe hypoxic ischemic encephalopathy (HIE). Study Des
Externí odkaz:
https://doaj.org/article/e4c76d2ce5584bc687cb0843a2a2ea65
Autor:
Kimberly M. Thornton, Timothy Bennett, Vivekanand Singh, Neil Mardis, Jennifer Linebarger, Howard Kilbride, Kristin Voos
Publikováno v:
Case Reports in Pediatrics, Vol 2014 (2014)
Diprosopus is a rare congenital malformation associated with high mortality. Here, we describe a patient with diprosopus, multiple life-threatening anomalies, and genetic mutations. Prenatal diagnosis and counseling made a beneficial impact on the fa
Externí odkaz:
https://doaj.org/article/c7fc30a25dc345b4810c7c9e337f17e5
Autor:
Kimberly M. Thornton, Michael F. Nyp, Lejla Music Aplenc, Gary L. Jones, Shannon L. Carpenter, Erin M. Guest, Steven M. Shapiro, Winston M. Manimtim
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
We present an unusual case of hyperbilirubinemia with rapid early progression leading to bilirubin encephalopathy in a term neonate. Despite early recognition and intervention, the total serum bilirubin reached a maximum level of 39 mg/dL at 32 hours
Externí odkaz:
https://doaj.org/article/127c372db9424569a2aea96c847c7320
Autor:
Winston M Manimtim, Lejla Music Aplenc, Gary L. Jones, Shannon L. Carpenter, Kimberly M. Thornton, Michael F. Nyp, Steven M. Shapiro, Erin M. Guest
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2013 (2013)
Case Reports in Pediatrics, Vol 2013 (2013)
We present an unusual case of hyperbilirubinemia with rapid early progression leading to bilirubin encephalopathy in a term neonate. Despite early recognition and intervention, the total serum bilirubin reached a maximum level of 39 mg/dL at 32 hours
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5aaa5c72ecf0e4cd1021fba9a3b4326
https://doi.org/10.1155/2013/284029
https://doi.org/10.1155/2013/284029
Autor:
Kristin Voos, Neil J. Mardis, Kimberly M. Thornton, Timothy L. Bennett, Jennifer Linebarger, Vivekanand Singh, Howard W. Kilbride
Publikováno v:
Case Reports in Pediatrics, Vol 2014 (2014)
Case Reports in Pediatrics
Case Reports in Pediatrics
Diprosopus is a rare congenital malformation associated with high mortality. Here, we describe a patient with diprosopus, multiple life-threatening anomalies, and genetic mutations. Prenatal diagnosis and counseling made a beneficial impact on the fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a7cfe84128e3888bc85db4c5dc06ab
https://doaj.org/article/c7fc30a25dc345b4810c7c9e337f17e5
https://doaj.org/article/c7fc30a25dc345b4810c7c9e337f17e5