Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Terianne, Lindsey"'
Autor:
Catherine R. Hoyt, Allison A. King, Terianne Lindsey, Chih Hung Chang, Regina A. Abel, Allison J. L’Hotta
Publikováno v:
Child: care, health and developmentREFERENCES. 46(5)
Background Children with sickle cell disease (SCD) are at risk for fine motor (FM) delays; however, screening for FM impairments is not common among young children with SCD. The Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371e0a1638e1922f459c0b2df34f8380
https://pubmed.ncbi.nlm.nih.gov/32599661
https://pubmed.ncbi.nlm.nih.gov/32599661
Autor:
Catherine R. Hoyt, Allison A. King, Regina A. Abel, Allison J. L’Hotta, Chih Hung Chang, Terianne Lindsey
Publikováno v:
Archives of Physical Medicine and Rehabilitation. 100:e142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2902ef6250541da46b12bc5c4a2a2c41
https://doi.org/10.1016/j.apmr.2019.08.435
https://doi.org/10.1016/j.apmr.2019.08.435
Publikováno v:
Journal of health disparities research and practice. 9(3)
Sickle cell trait (SCT) screening is required at birth in the United States; however, adults rarely know their SCT status prior to having children.Assess feasibility of a community-based SCT education and testing intervention.Participants were recrui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bcf4ee6d24f4df6f904e3652053e229
https://pubmed.ncbi.nlm.nih.gov/27774352
https://pubmed.ncbi.nlm.nih.gov/27774352
Autor:
Lisa Swinton McLaughlin, John Theus, Michael R. DeBaun, Terianne Lindsey, Mary Robbins, David Baker, Keri Jupka, Ricardo J. Wray, Brittany Covert, Dionna O. Roberts, Vincent Edwards
Publikováno v:
Immunohematology. 28:7-12
In children with sickle cell disease (SCD), primary and secondary prevention of strokes require indefinite regular blood transfusion therapy. The risks associated with repeated transfusions include alloimmunization and increased donor exposure. The C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d29c61c1c56aed74cb05b001bbe40dad
https://doi.org/10.21307/immunohematology-2019-141
https://doi.org/10.21307/immunohematology-2019-141
Publikováno v:
Immunohematology. 22:112-116
Sickle cell disease (SCD) is an inherited blood disorder which can be complicated by stroke in infancy and childhood. The primary and secondary prevention of stroke in this patient population is regular RBC transfusion therapy at least every three we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ded4e3604bbee705309bdc4b8c54baac
https://doi.org/10.21307/immunohematology-2019-366
https://doi.org/10.21307/immunohematology-2019-366
Publikováno v:
Pediatric Blood & Cancer. 55:554-556
The objective of this study is to determine the prevalence of adherence to daily medications among children with sickle cell disease (SCD). Prescription records for 12 months were obtained from participants who had insurance in a Medicaid-based singl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0ae250a1357dc04112c29d7662223d9
https://doi.org/10.1002/pbc.22605
https://doi.org/10.1002/pbc.22605
Autor:
Diane Calamaras, Michael R. DeBaun, Terianne Lindsey, Gwendolyn Lea, Melissa Phillips, Janice Beatty, Julie Routhieaux, Nutrena Watts‐Tate, Elaine Southwood, Evelyn Brown
Publikováno v:
Journal of the American Academy of Nurse Practitioners. 17(7)
Purpose To identify variations in practices used by nurses for pediatric patients with sickle cell disease (SCD) receiving chronic blood transfusion therapy for strokes. Data sources Descriptive study of a convenience sample of 11 nurses who care for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f69319c243b15ba8f79d89b2df9a775f
https://pubmed.ncbi.nlm.nih.gov/15982248
https://pubmed.ncbi.nlm.nih.gov/15982248