Zobrazeno 1 - 7
of 7
pro vyhledávání: '"S. Barron Frazier"'
Publikováno v:
JEM Reports, Vol 2, Iss 1, Pp 100011- (2023)
Background: Croup encounters substantially decreased when the pandemic first began, specifically between March and September 2020, before croup cases dramatically spiked again with the Omicron variant. There is a dearth of information concerning chil
Externí odkaz:
https://doaj.org/article/f6d9e66fd75d442ba9373446d452ebe5
Autor:
Kathleen Doherty, S. Barron Frazier, Matthew Clark, Anna Childers, Sumit Pruthi, David A. Wenger, Jessica Duis
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 19, Iss , Pp - (2019)
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease mainly caused by a deficiency of arylsulfatase A activity. The typical clinical course of patients with the late infantile form includes a regression in motor skil
Externí odkaz:
https://doaj.org/article/1e6234d8bbac4e01a18b31c831e9365a
Autor:
S Barron, Frazier, Michele, Walsh, Glory, Beveridge, Clark, Thornton, Jaime Kaye, Otillio, Emily, Fain, Barron, Patterson
Publikováno v:
Hospital Pediatrics. 12:726-734
BACKGROUND Clinician documentation is highly variable, and awareness of documentation requirements remains low despite post-training experience. At our hospital, critical care (CC) documentation was inconsistent. Our aim was to increase appropriate C
External validation of a clinical prediction rule for very low risk pediatric blunt abdominal trauma
Publikováno v:
The American Journal of Emergency Medicine. 37:1643-1648
Background Computed tomography (CT) is frequently used to identify intra-abdominal injuries in children with blunt abdominal trauma (BAT). The Pediatric Emergency Care Applied Research Network (PECARN) proposed a prediction rule to identify children
Autor:
S. Barron Frazier, James C. Gay, Shari Barkin, Michelle Graham, Michele Walsh, Kathryn Carlson
Publikováno v:
Healthcare (Amsterdam, Netherlands). 10(3)
Previous interventions to reduce emergency department (ED) overutilization from non-urgent visits have shown little success. At our hospital, we created an ED to primary care clinic (PCC) transfer protocol for non-urgent ED visits of established pati
Autor:
Matthew Clark, S. Barron Frazier, Jessica Duis, Sumit Pruthi, David A. Wenger, Kathleen M. Doherty, Anna Childers
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 19, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports, Vol 19, Iss, Pp-(2019)
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease mainly caused by a deficiency of arylsulfatase A activity. The typical clinical course of patients with the late infantile form includes a regression in motor skil
Publikováno v:
Clinical Pediatrics. 57:1120-1122