Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Wendy S Darlington"'
Autor:
Mary Dang, Noel Cercizi, Lena Elmuti, Josephine Jung, Christine Timmer, Wendy S Darlington, Diana Kinn, Kumar Madan, Radhika Peddinti, Marie-Ellen Sarvida, Gabrielle Lapping-Carr
Publikováno v:
Blood. 140:2584-2585
Area of Residence As a Screening Tool for Sickle Cell Disease Outcomes in Chicago Pediatric Patients
Autor:
Sharjeel Syed, Kristen Wroblewski, Radhika Peddinti, Gabrielle Lapping-Carr, Wendy S Darlington
Publikováno v:
Blood. 140:8218-8219
Autor:
Wendy S Darlington, Adam L. Green
Publikováno v:
CancerReferences. 127(19)
Autor:
Radhika Peddinti, Gabrielle Lapping-Carr, Kristen Wroblewski, Sharjeel Syed, Wendy S Darlington
Publikováno v:
Blood. 138:972-972
Sickle cell disease (SCD) is a chronic, debilitating condition that negatively impacts patient quality of life (QOL). In addition to causing frequent crises that lead patients to seek medical attention, it can also exacerbate socioeconomic inequities
Publikováno v:
Pediatric Blood & Cancer. 62:2232-2234
Children undergoing intense cancer treatment frequently require total parenteral nutrition (TPN). Rarely, vitamins are removed due to hypersensitivity to the carrier vehicle in the formulation. We present the case of a 5-year-old patient with stage 4
Autor:
Stephanie M. Rangel, David Gozal, Abdelnaby Khalyfa, Wendy S Darlington, Eric C. Beyer, Radhika Peddinti, John M. Cunningham, Gabrielle Lapping-Carr
Publikováno v:
Pediatric pulmonology. 52(11)
Background Acute Chest Syndrome (ACS) is one of the leading causes of death among children with Sickle Cell Disease (SCD). Disruption of microvascular integrity is critical to the pathophysiology of ACS, but the factors governing its phenotypic varia
Autor:
Tanisha Jones, Wendy S Darlington, Shelby Gruntorad, Radhika Peddinti, Gabrielle Lapping-Carr
Publikováno v:
Blood. 132:2283-2283
Introduction: Sickle cell disease (SCD) is a genetic disorder affecting approximately 100,000 individuals in the United States. This autosomal recessive condition can result in numerous acute and chronic complications. Current research is ongoing to
Publikováno v:
Blood. 132:2385-2385
Introduction: Sickle cell disease (SCD) is a genetic disorder diagnosed at birth, characterized by repeated acute complications leading to significant morbidity and mortality. Patients subjectively state extreme temperatures trigger sickle cell compl
Autor:
Gabrielle Lapping-Carr, Shelby Gruntorad, Joanna Gemel, Rebecca Sturey, Radhika Peddinti, Margaret Harrington, Eric C. Beyer, Gianna Sparks, Wendy S Darlington, Yifan Mao
Publikováno v:
Blood. 132:2363-2363
Introduction: Acute chest syndrome (ACS) is a leading cause of morbidity and death among children with sickle cell disease (SCD). Aberrant cell-cell interactions involving the endothelium are central to the pathophysiology of ACS. Endothelial integri
Publikováno v:
Pediatric bloodcancer. 62(12)
Children undergoing intense cancer treatment frequently require total parenteral nutrition (TPN). Rarely, vitamins are removed due to hypersensitivity to the carrier vehicle in the formulation. We present the case of a 5-year-old patient with stage 4