Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Angela B Snyder"'
Autor:
Ashima Singh, Marci K Sontag, Mei Zhou, Mahua Dasgupta, Tessa Crume, Morgan McLemore, Najibah Galadanci, Eldrida Randall, Nicole Steiner, Amanda M Brandow, Kathryn Koch, Joshua J Field, Kathryn Hassell, Angela B Snyder, Julie Kanter
Publikováno v:
JMIR Public Health and Surveillance, Vol 9, p e42816 (2023)
BackgroundSickle cell disease (SCD) was first recognized in 1910 and identified as a genetic condition in 1949. However, there is not a universal clinical registry that can be used currently to estimate its prevalence. The Sickle Cell Data Collection
Externí odkaz:
https://doaj.org/article/51153b4dc3cd4bc1a0b470e84e02cfcf
Autor:
Amy Y. Tang, Mei Zhou, Alexander N. Maillis, Kristina W. Lai, Peter A. Lane, Angela B. Snyder
Publikováno v:
Pediatric bloodcancerREFERENCES.
There have been significant changes in clinical guidelines for sickle cell disease (SCD) over the past two decades, including updated indications for hydroxyurea, transfusions, and iron overload management. In practice however, there are few studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bc40623bc0d8d94cbab783c4477d772
https://pubmed.ncbi.nlm.nih.gov/36579749
https://pubmed.ncbi.nlm.nih.gov/36579749
Autor:
Angela B. Snyder, Sangeetha Lakshmanan, Mary M. Hulihan, Susan T. Paulukonis, Mei Zhou, Sophia S. Horiuchi, Karon Abe, Shammara N. Pope, Laura A. Schieve
Publikováno v:
Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002). 71(9)
Sickle cell disease (SCD), an inherited blood disorder affecting an estimated 100,000 persons in the United States, is associated with multiple complications and reduced life expectancy. Complications of SCD can include anemia, debilitating acute and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1519e076abd9ebb89ce23187ce745e5b
https://pubmed.ncbi.nlm.nih.gov/36201430
https://pubmed.ncbi.nlm.nih.gov/36201430
Autor:
Ashima Singh, Marci K Sontag, Mei Zhou, Mahua Dasgupta, Tessa Crume, Morgan McLemore, Najibah Galadanci, Eldrida Randall, Nicole Steiner, Amanda M Brandow, Kathryn Koch, Joshua J Field, Kathryn Hassell, Angela B Snyder, Julie Kanter
BACKGROUND Sickle cell disease (SCD) was first recognized in 1910 and identified as a genetic condition in 1949. However, there is not a universal clinical registry that can be used currently to estimate prevalence. The Sickle Cell Data Collection (S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23a59043e522ad1ef45c9a359678d893
https://doi.org/10.2196/preprints.42816
https://doi.org/10.2196/preprints.42816
Autor:
Brandon K. Attell, Allison P. Plaxco, Mei Zhou, Jhaqueline Valle, Sarah L. Reeves, Pooja N. Patel, Krista Latta, Matthew P. Smeltzer, Angela B. Snyder
Publikováno v:
BMC Emergency Medicine, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background The emergency department (ED) is a vital source of healthcare for individuals living with sickle cell disease (SCD). Prior research indicates that during the COVID-19 pandemic some individuals with SCD avoided the ED for fear of a
Externí odkaz:
https://doaj.org/article/5dfde016853e47879027052b10f25b03
Autor:
Brandon K. Attell, PhD, Patricia M. Barrett, MS, Betty S. Pace, MD, Morgan L. McLemore, MD, Blake T. McGee, PhD, Rewo Oshe, BS, Ann M. DiGirolamo, PhD, Lindsey L. Cohen, PhD, Angela B. Snyder, PhD
Publikováno v:
AJPM Focus, Vol 3, Iss 1, Pp 100158- (2024)
Introduction: Individuals living with sickle cell disease experience high levels of morbidity that result in frequent utilization of the emergency department. The objective of this study was to provide updated national estimates of emergency departme
Externí odkaz:
https://doaj.org/article/b46c336d2c8a49bc9a885fec14609a32