Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Robert I, Liem"'
Autor:
Robert I. Liem, Sophie Lanzkron, Thomas D. Coates, Laura DeCastro, Ankit A. Desai, Kenneth I. Ataga, Robyn T. Cohen, Johnson Haynes, Jr, Ifeyinwa Osunkwo, Jeffrey D. Lebensburger, James P. Lash, Theodore Wun, Madeleine Verhovsek, Elodie Ontala, Rae Blaylark, Fares Alahdab, Abdulrahman Katabi, Reem A. Mustafa
Publikováno v:
Blood Advances, Vol 3, Iss 23, Pp 3867-3897 (2019)
Abstract: Background: Prevention and management of end-organ disease represent major challenges facing providers of children and adults with sickle cell disease (SCD). Uncertainty and variability in the screening, diagnosis, and management of cardiop
Externí odkaz:
https://doaj.org/article/103e3c28d1ea4d3a8494c2017edd08e9
Autor:
M. Hassan Murad, Robert I. Liem, Eddy S. Lang, Elie A. Akl, Joerg J. Meerpohl, Michael R. DeBaun, John F. Tisdale, Amanda M. Brandow, Sophie M. Lanzkron, Stella T. Chou, Starr Webb, Reem A. Mustafa
Publikováno v:
Blood Advances, Vol 3, Iss 23, Pp 3945-3950 (2019)
Abstract: The American Society of Hematology (ASH) convened 5 guideline panels to develop clinical practice recommendations addressing 5 management areas of highest importance to individuals living with sickle cell disease: pain, cerebrovascular comp
Externí odkaz:
https://doaj.org/article/4e444d45665b485eb92c3039cd8de264
Autor:
Sophie Lanzkron, Gregory S. Sawicki, Kathryn L. Hassell, Michael W. Konstan, Robert I. Liem, Susanna A. McColley
Publikováno v:
Journal of Clinical and Translational Science, Vol 2, Pp 334-342 (2018)
AbstractIntroductionA growing population of adults living with severe, chronic childhood-onset health conditions has created a need for specialized health care delivered by providers who have expertise both in adult medicine and in those conditions.
Externí odkaz:
https://doaj.org/article/9df7239eaa9e4b1283fb0be6a33db9be
Autor:
Sherif M. Badawy, Alexis A. Thompson, Jin-Shei Lai, Frank J. Penedo, Karen Rychlik, Robert I. Liem
Publikováno v:
Health and Quality of Life Outcomes, Vol 15, Iss 1, Pp 1-10 (2017)
Abstract Background Sickle cell disease (SCD) patients have impaired domains of health-related quality of life (HRQOL). Hydroxyurea is safe and efficacious in SCD; however, adherence is suboptimal, and patients’ perceptions are poorly understood am
Externí odkaz:
https://doaj.org/article/5a283c8e870f469c9ebc3cd1be0b92a5
Autor:
Julie A. Panepinto, J. Paul Scott, Oluwakemi Badaki-Makun, Deepika S. Darbari, Corrie E. Chumpitazi, Gladstone E. Airewele, Angela M. Ellison, Kim Smith-Whitley, Prashant Mahajan, Sharada A. Sarnaik, T Charles Casper, Larry J. Cook, Julie Leonard, Monica L. Hulbert, Elizabeth C. Powell, Robert I. Liem, Robert Hickey, Lakshmanan Krishnamurti, Cheryl A. Hillery, David C. Brousseau, for the Pediatric Emergency Care Applied Research Network (PECARN)
Publikováno v:
Health and Quality of Life Outcomes, Vol 15, Iss 1, Pp 1-12 (2017)
Abstract Background Detecting change in health status over time and ascertaining meaningful changes are critical elements when using health-related quality of life (HRQL) instruments to measure patient-centered outcomes. The PedsQL™ Sickle Cell Dis
Externí odkaz:
https://doaj.org/article/b1d79058e9f547768a11be8524b05535
Publikováno v:
Pediatric Cardiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ec3790ccdbd0328c1867ec19f1bb121
https://doi.org/10.1007/s00246-023-03112-1
https://doi.org/10.1007/s00246-023-03112-1
Autor:
F. Bernaudin, Damiano Rondelli, Julie Kanter, Teonna L Woolford, Julie A. Panepinto, Courtney D. Fitzhugh, John F. Tisdale, Javier Bolaños-Meade, Shalini Shenoy, Jane S. Hankins, John E. Wagner, Robert I. Liem, Mark C. Walters, Joerg J Meerpohl, M. Hassan Murad
Publikováno v:
Blood Adv
Background: Sickle cell disease (SCD) is a life-limiting inherited hemoglobinopathy that results in significant complications and affects quality of life. Hematopoietic stem cell transplantation (HSCT) is currently the only curative intervention for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac3d919db2b6834a23ec1ae56e76ad3
https://doi.org/10.1182/bloodadvances.2021004394c
https://doi.org/10.1182/bloodadvances.2021004394c
Heart rate variability associated with acute exercise challenge in children with sickle cell anaemia
Publikováno v:
Br J Haematol
We examined heart rate variability (HRV) during exercise testing in 20 children with sickle cell anaemia (SCA) and 12 controls. Subjects achieved lower median HRV at peak exercise [standard deviation of R-wave to R-wave intervals (SDNN), 2·3 vs 2·9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a143270f4e832c2f1894daa77648a531
https://doi.org/10.1111/bjh.17834
https://doi.org/10.1111/bjh.17834
Autor:
Christina M. Barriteau, Joe Feinglass, Mariam Kayle, Paige VonAchen, Robert I. Liem, Sherif M. Badawy, Kristin Kan
Publikováno v:
Pediatric hematology and oncology.
Sickle cell disease (SCD) state level surveillance data are limited. We performed a retrospective review of emergency department (ED) visits and hospitalizations from individuals with SCD in Illinois (2016-2020) using the Illinois Health and Hospital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11db696878468bd0ad8e76a445a45e43
https://pubmed.ncbi.nlm.nih.gov/35612367
https://pubmed.ncbi.nlm.nih.gov/35612367
Autor:
Susan E. Creary, Chase Beeman, Joseph Stanek, Kathryn King, Patrick T. McGann, Sarah H. O'Brien, Robert I. Liem, Jane Holl, Sherif M. Badawy
Publikováno v:
Pediatr Blood Cancer
BACKGROUND: Hydroxyurea is the primary treatment for sickle cell anemia (SCA), yet real-world implementation in high-income settings is suboptimal. Variation in prescribed hydroxyurea dose and patient adherence in these settings can both affect actua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3296dab07b0c5bbdc97fdc0419575b4a
https://doi.org/10.1002/pbc.29607
https://doi.org/10.1002/pbc.29607