Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Stephanie O Ibemere"'
Autor:
Tolu O Oyesanya, Stephanie O Ibemere, HyunBin You, Maralis Mercado Emerson, Wei Pan, Anushka Palipana, Melissa Kandel, Darius Ingram, Mayra Soto, Anne Pioppo, Brittany Albert, Tamia Walker-Atwater, Jodi Hawes, Jordan Komisarow, Katherine Ramos, Lindsey Byom, Rosa Gonzalez-Guarda, Courtney H Van Houtven, Suresh Agarwal, Janet Prvu Bettger
Publikováno v:
PLoS ONE, Vol 19, Iss 2, p e0296083 (2024)
ObjectiveThe purpose of this study is to examine the efficacy of BETTER (Brain Injury, Education, Training, and Therapy to Enhance Recovery) vs. usual transitional care management among diverse adults with traumatic brain injury (TBI) discharged home
Externí odkaz:
https://doaj.org/article/7e97fdc526554f6ebb0dac1558c91238
Autor:
Stephanie O. Ibemere, Paula Tanabe, Emily Bonnabeau, Gary Rains, Kern Eason, Marian F. Earls, Nirmish Shah
Publikováno v:
Journal of Primary Care & Community Health, Vol 12 (2021)
Background Sickle cell disease (SCD) is a complex chronic blood disorder characterized by severe disease complications ideally managed by both hematologists and primary care providers (PCP’s). PCP’s report knowledge gaps and discomfort with SCD m
Externí odkaz:
https://doaj.org/article/44c5499d24e34fd0834b2ed8f6723577
Autor:
Tolu O. Oyesanya, Stephanie O. Ibemere, Callan Loflin, Victoria McReynolds, Brian Anaya, Michelle Huang, Rosa Gonzalez-Guarda, Timothy J. Strauman, Janet Prvu Bettger
Publikováno v:
Brain Injury. :1-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a507969eb6b2b3a11651a769565e758
https://doi.org/10.1080/02699052.2023.2208881
https://doi.org/10.1080/02699052.2023.2208881
Autor:
Stephanie O, Ibemere, Charity I, Oyedeji, Liliana, Preiss, Laura E, Van Althuis, Jane S, Hankins, Melissa, Azul, Ebony N, Burns, Jeffrey, Glassberg, Ward, Hagar, Faiz, Hussain, Allison, King, Cathy, Melvin, John, Myers, Angela, Snyder, Nirmish, Shah, Paula, Tanabe
Publikováno v:
British Journal of Haematology. 200:633-642
Individuals with sickle cell disease (SCD) have historically been considered underweight. Despite increasing body mass index (BMI) in the general population, the prevalence of overweight and obese status remains unclear in the adult SCD population. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ae2413e53550300bab34a7022b0148
https://doi.org/10.1111/bjh.18548
https://doi.org/10.1111/bjh.18548
Autor:
Marian Earls, Emily Bonnabeau, Kern Eason, Nirmish Shah, Gary Rains, Stephanie O Ibemere, Paula Tanabe
Publikováno v:
Journal of Primary Care & Community Health
Journal of Primary Care & Community Health, Vol 12 (2021)
Journal of Primary Care & Community Health, Vol 12 (2021)
Background Sickle cell disease (SCD) is a complex chronic blood disorder characterized by severe disease complications ideally managed by both hematologists and primary care providers (PCP’s). PCP’s report knowledge gaps and discomfort with SCD m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab7fabb20e2dcf490a3a882224b4804
http://europepmc.org/articles/PMC8512219
http://europepmc.org/articles/PMC8512219
Publikováno v:
Qualitative health research. 31(8)
Sickle cell disease (SCD) is a chronic genetic disease that causes life-threatening complications and requires robust comprehensive management. Developing comprehensive SCD programs in sub-Saharan African countries requires knowledge of the cultural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e59f1fd4dc56cbc8827cb365d754da8c
https://pubmed.ncbi.nlm.nih.gov/34018867
https://pubmed.ncbi.nlm.nih.gov/34018867
Autor:
Charity I Oyedeji, Allison A. King, Angela Snyder, Liliana Preiss, Ebony Burns, Cathy L. Melvin, John Myers, Jane S. Hankins, Stephanie O Ibemere, Nirmish Shah, Jeffrey Glassberg, Melissa Azul, Robert Ward Hagar, Paula Tanabe, Faiz Ahmed Hussain, Laura E. Niederer
Publikováno v:
Blood. 138:2039-2039
Introduction Emerging literature suggests body mass index (BMI) may be increasing in individuals with sickle cell disease (SCD), a condition historically associated with underweight status. However, the current prevalence of overweight and obese adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c4713ff2e739847e6340856687362da
https://doi.org/10.1182/blood-2021-146265
https://doi.org/10.1182/blood-2021-146265
Autor:
Caroline E Freiermuth, Stephanie O Ibemere, Sarah B. Dubbs, Huiman X. Barnhart, Paula Tanabe, John J. Strouse, R. Gentry Wilkerson, Jacqueline L Brown, Judith A. Paice, Patricia L. Kavanagh, Compare-Voe study investigators
Publikováno v:
Contemp Clin Trials
Objectives Painful vaso-occlusive episodes (VOE) are the most common reason for emergency department (ED) visits experienced by patients with sickle cell disease (SCD). The National Heart, Lung and Blood Institute (NHLBI) evidence-based recommendatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5810bf0e502e363dc2efaee2d3638219
https://doi.org/10.1016/j.cct.2020.106252
https://doi.org/10.1016/j.cct.2020.106252