Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Regina D. Crawford"'
Autor:
Paula Tanabe, Hayden B. Bosworth, Regina D. Crawford, Jeffrey Glassberg, Christopher N. Miller, Judith A. Paice, Susan Silva
Publikováno v:
European Journal of Haematology. 110:518-526
Compare time to pain relief (minimum of a 13 mm and 30% reduction) during an Emergency Department (ED) visit among patients with sickle cell disease (SCD) experiencing severe pain associated with a vaso-occlusive episode who were randomized to receiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::320eb901eb2c9a351b7bed827c227399
https://doi.org/10.1111/ejh.13924
https://doi.org/10.1111/ejh.13924
Publikováno v:
Journal of the National Medical Association. 113(2)
Individuals with hemoglobinopathies experience complications that often require management with multiple transfusions. These chronic transfusions can lead to iron overload, which places them at increased risk of organ damage, malignancy, and even dea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f6eacb721efff950ffe89f6746ec20
https://pubmed.ncbi.nlm.nih.gov/32892996
https://pubmed.ncbi.nlm.nih.gov/32892996
Autor:
Sarah Rapisardo, Anand S. Lagoo, Endi Wang, Yue Zhao, Chad M. McCall, Jadee L. Neff, Lian-He Yang, Jake Maule, Regina D. Crawford, Yang Li
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 32(12)
Myeloid neoplasms occasionally occur in patients with sickle cell disease, and the underlying connection between the two diseases is unclear. Herein, we retrospectively analyzed four cases of sickle cell disease patients who developed myeloid neoplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55931c4bcf0eb195e82fa3d8abccb3a3
https://pubmed.ncbi.nlm.nih.gov/31371806
https://pubmed.ncbi.nlm.nih.gov/31371806
Autor:
Christopher N. Miller, LaʼKita M J Knight, Hayden B. Bosworth, Jeffrey Glassberg, Lynne D. Richardson, Regina D. Crawford, Elijah O. Onsomu, Paula Tanabe, Theresa DeMartino, Judith A. Paice
INTRODUCTION: Treatment of vaso-occlusive episodes (VOE) are the most common reason for ED treatment of sickle cell disease (SCD). We 1) compared perceptions of the usability and ability to manage VOE pain between ED nurses and other ED provider type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a599c14c10286c7927cfd245e5d4417
https://europepmc.org/articles/PMC6361535/
https://europepmc.org/articles/PMC6361535/
Publikováno v:
Journal of Advanced Nursing. 72:1409-1416
Aims This study aimed to: (1) evaluate cognitive function among adults with sickle cell disease using a computer-administered neuropsychological test; and (2) replicate previously identified differences in processing speed between patients with sickl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09e2bab4fdd1a872ef330bf867df0f0
https://doi.org/10.1111/jan.12755
https://doi.org/10.1111/jan.12755
Autor:
Susan G. Silva, Hayden B. Bosworth, Jeffrey Glassberg, Christopher N. Miller, Judith A. Paice, Paula Tanabe, Regina D. Crawford, Lynne D. Richardson
Publikováno v:
American journal of hematology. 93(2)
SCD is the most common genetic disorder in the United States and occurs primarily among African Americans. The cardinal clinical manifestation of SCD and most common reason for emergency department (ED) visits is the painful, vaso-occlusive episode (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b19687e90bd08ad43fad0fdbc443b96a
https://pubmed.ncbi.nlm.nih.gov/29047145
https://pubmed.ncbi.nlm.nih.gov/29047145
Publikováno v:
Journal of the National Medical Association. 104:459-462
Kikuchi-Fugimoto's Disease (KFD), also known as histiocytic necrotizing lymphadenitis, is most frequently seen in young women and has been associated with autoimmune disorders such as polymyositis and systemic lupus erythematosus. It is generally a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41be197bcbc43a3b043d88e9b5d1a314
https://doi.org/10.1016/s0027-9684(15)30201-7
https://doi.org/10.1016/s0027-9684(15)30201-7
Autor:
Regina D. Crawford, Christopher M. Miller, Jeffrey Glassberg, Susan G. Silva, Hayden B. Bosworth, Christopher Barczak, Adam A. Soliman, Theresa DeMartino, Paula Tanabe
Publikováno v:
Blood. 128:3674-3674
Introduction: Vaso-occlusive episodes are the most common complication experienced by individuals with sickle cell disease (SCD). Treatment in an emergency department (ED) is often required and significant variability in care exists. In 2014, NHLBI p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec02a6a59641b70a5770d4ce6bce6de2
https://doi.org/10.1182/blood.v128.22.3674.3674
https://doi.org/10.1182/blood.v128.22.3674.3674
Autor:
Regina D. Crawford, Rupa Redding-Lallinger, Valerie Jewells, April Edwards, E. Leila Jerome Clay, Stacie D Adams
Publikováno v:
Journal of Medical Case Reports
Introduction Vasculopathy of the large vessels commonly occurs in sickle cell disease, and as a result cerebral infarction is a well characterized complication of this condition. However, spinal infarction appears to be rare. Spinal infarct is infreq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e671c0ca819a7c21121887db81edc6dd
https://doi.org/10.1186/1752-1947-7-210
https://doi.org/10.1186/1752-1947-7-210