Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anjelica C. Saulsberry"'
Publikováno v:
Neurobiology of Disease, Vol 100, Iss , Pp 87-98 (2017)
This study assessed the extent to which high fat diet (HFD)-induced β-amyloid accumulation and cognitive decline in APP/PSEN1 mice are reversible through control of fat intake. Ten months of HFD (60% calories from fat) led to significant deficits in
Externí odkaz:
https://doaj.org/article/7b2ad48787404dca81ac929785226bd1
Publikováno v:
Hematology Am Soc Hematol Educ Program
Most children with sickle cell disease (SCD) today survive into adulthood. Among emerging adults, there is a marked increase in acute care utilization and a rise in mortality, which can be exacerbated by not establishing or remaining in adult care. H
Autor:
Sheila Anderson, Jason R. Hodges, Jerlym S. Porter, Jane S. Hankins, Kristen E. Howell, Anjelica C. Saulsberry-Abate, Vikki G. Nolan, Joacy G. Mathias, Kenneth I. Ataga
Publikováno v:
Pediatr Blood Cancer
BACKGROUND/OBJECTIVES: Care continuity prevents increased health care utilization and mortality during transition from pediatric to adult care. Our program employs a co-located care delivery model, in which pediatric provider involvement continues du
Autor:
Jerlym S. Porter, Lisa M. Jacola, Jane E. Schreiber, Winfred C. Wang, Allison A. King, Guolian Kang, Pradeep S. B. Podila, Anjelica C. Saulsberry-Abate, Xiwen Zhao, Jane S. Hankins, Marita Partanen, Jason R. Hodges
Publikováno v:
Br J Haematol
Neurocognitive deficits in sickle cell disease (SCD) may impair adult care engagement. We investigated the relationship between neurocognitive functioning and socio-environmental factors with healthcare transition outcomes. Adolescents aged 15-18 yea
Publikováno v:
JMIR Pediatrics and Parenting
JMIR Pediatrics and Parenting, Vol 3, Iss 1, p e15093 (2020)
JMIR Pediatrics and Parenting, Vol 3, Iss 1, p e15093 (2020)
Background Advancements in treatment have contributed to increased survivorship among children with sickle cell disease (SCD). Increased transition readiness, encompassing disease knowledge and self-management skills before transfer to adult care, is
Publikováno v:
Neurobiology of Disease, Vol 100, Iss, Pp 87-98 (2017)
This study assessed the extent to which high fat diet (HFD)-induced β-amyloid accumulation and cognitive decline in APP/PSEN1 mice are reversible through control of fat intake. Ten months of HFD (60% calories from fat) led to significant deficits in
BACKGROUND Advancements in treatment have contributed to increased survivorship among children with sickle cell disease (SCD). Increased transition readiness, encompassing disease knowledge and self-management skills before transfer to adult care, is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51603c4e505dcfd37b8b9562a310d4fd
https://doi.org/10.2196/preprints.15093
https://doi.org/10.2196/preprints.15093
Autor:
Jason R. Hodges, Lisa M. Jacola, Guolian Kang, Winfred C. Wang, Allison A. King, Jane S. Hankins, Xiwen Zhao, Jerlym S. Porter, Marita Partanen, Pradeep S. B. Podila, Anjelica C. Saulsberry
Publikováno v:
Blood. 134:519-519
Introduction: In the United States, most children with sickle cell disease (SCD) survive into adulthood and transfer from pediatric to adult-centered care. Cognitive deficits begin during childhood and are highly prevalent among individuals with SCD,
Autor:
Vikki G. Nolan, Sheila Anderson, Kristen E. Howell, Kenneth I. Ataga, Jane S. Hankins, Joacy G. Mathias, Jason R. Hodges, Jerlym S. Porter, Anjelica C. Saulsberry
Publikováno v:
Blood. 134:4676-4676
Introduction: During transition from pediatric to adult care, young adults with sickle cell disease (SCD) experience increased acute healthcare utilization and mortality. Functional transitional programs maintain care quality; however, there is a dea
Autor:
Jerlym S. Porter, Anjelica C. Saulsberry, Jason R. Hodges, Pradeep S. B. Podila, Shiela Anderson, Jane S. Hankins
Publikováno v:
Blood. 132:5820-5820
Introduction: Unsuccessful transition from pediatric to adult care among youth with sickle cell disease (SCD) contributes to frequent disease complications and early death. The literature is sparse on longitudinal SCD transition program outcomes. The