Search Results - "Oneal, Patricia"
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FDA Approval Summary: Vemurafenib for the Treatment of Patients with Erdheim‐Chester Disease with the BRAFV600 Mutation
Published in The oncologist (Dayton, Ohio) (01-12-2018)“…On November 6, 2017, the U.S. Food and Drug Administration (FDA) granted regular approval to vemurafenib for the treatment of adult patients with…”
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High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin
Published in Nature medicine (01-09-2007)“…In thalassemia, deficient globin-chain production during erythropoiesis results in anemia. Thalassemia may be further complicated by iron overload (frequently…”
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3
Acute chest syndrome: sickle cell disease
Published in European journal of haematology (01-09-2011)“…Acute chest syndrome (ACS) is a common complication and reason for hospital admission in patients with sickle cell disease (SCD). It is also the most common…”
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FDA Approval Summary: Vemurafenib for the Treatment of Patients with Erdheim-Chester Disease with the BRAF V600 Mutation
Published in The oncologist (Dayton, Ohio) (01-12-2018)“…On November 6, 2017, the U.S. Food and Drug Administration (FDA) granted regular approval to vemurafenib for the treatment of adult patients with…”
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5
Multicenter COMPACT study of COMplications in Patients with sickle cell disease And utilization of iron Chelation Therapy
Published in Current medical research and opinion (01-03-2015)“…Abstract Background: Over the past few decades, lifespans of sickle cell disease (SCD) patients have increased; hence, they encounter multiple complications…”
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Pernicious Anemia with Autoimmune Hemolytic Anemia: A Case Report and Literature Review
Published in Case reports in hematology (01-01-2016)“…Pernicious anemia is a common cause of vitamin B12 deficiency. Here, we discuss a case of a young woman who presented with severe anemia along with a history…”
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Increased iron export by ferroportin induces restriction of HIV-1 infection in sickle cell disease
Published in Blood advances (27-12-2016)“…The low incidence of HIV-1 infection in patients with sickle cell disease (SCD) and inhibition of HIV-1 replication in vitro under the conditions of low…”
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Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming
Published in Blood (10-09-2009)“…Therapeutic regulation of globin genes is a primary goal of translational research aimed toward hemoglobinopathies. Signal transduction was used to identify…”
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Hepatoid Adenocarcinoma of the Duodenum: An Unusual Location
Published in Case reports in oncology (12-03-2016)“…Hepatoid adenocarcinoma (HAC) is a rare extrahepatic tumor distinguished by having both hepatoid and adenomatous features, which can make the diagnosis…”
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Prevalence of Sickle Cell Trait and Rare Hemoglobin Variants in the Metropolitan Washington DC Area
Published in Journal of hematology (01-09-2020)Get full text
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End points for sickle cell disease clinical trials: patient-reported outcomes, pain, and the brain
Published in Blood advances (10-12-2019)“…To address the global burden of sickle cell disease (SCD) and the need for novel therapies, the American Society of Hematology partnered with the US Food and…”
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Aromatase Inhibitor-Induced Erythrocytosis in a Patient Undergoing Hormonal Treatment for Breast Cancer
Published in Case reports in hematology (01-01-2015)“…Aromatase inhibitors (AIs) are most commonly used for breast cancer patients with hormone receptor positive disease. Although the side effect profile of…”
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13
Fetal hemoglobin silencing in humans
Published in Blood (15-09-2006)“…Interruption of the normal fetal-to-adult transition of hemoglobin expression should largely ameliorate sickle cell and beta-thalassemia syndromes. Achievement…”
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Sepsis caused by Mycobacterium terrae complex in a patient with sickle cell disease
Published in BMJ case reports (02-05-2013)“…Infections are a significant cause of morbidity and mortality in patients with sickle cell disease. Loss of splenic function in these patients makes them…”
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End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings
Published in Blood advances (10-12-2019)“…To address the global burden of sickle cell disease and the need for novel therapies, the American Society of Hematology partnered with the US Food and Drug…”
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Faculty Perspective on Interprofessional Education Competencies: Respiratory Therapy Compared to Other Allied Health Professions
Published in Respiratory care (01-10-2022)“…Interprofessional Education (IPE) provides a framework for collaborative education between health care specialties to improve patient care. In 2010, the…”
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A Novel Use of Early Radiation Therapy in the Treatment of Hyperbilirubinemia in a Patient with Primary Hepatic Lymphoma and Chronic Hepatitis C
Published in Case reports in gastrointestinal medicine (01-01-2014)“…Lymphomas arising in the liver are extremely rare. Here, we describe a case of Hepatitis C virus infection with primary hepatic lymphoma (PHL) presenting with…”
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Inhibition of erythroblast growth and fetal hemoglobin production by ribofuranose-substituted adenosine derivatives
Published in Biochimica et biophysica acta (01-09-2008)“…In vivo, inhibition of fetal hemoglobin (HbF) expression in humans around the time of birth causes the clinical manifestation of sickle cell and…”
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Hydroxycarbamide treatment in sickle cell disease: estimates of possible leukaemia risk and of hospitalization survival benefit
Published in British journal of haematology (01-12-2014)“…Summary Using health insurance claims databases we compared the frequency/incidence of acute myeloid leukaemia (AML) and inpatient mortality in sickle cell…”
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Survival Among Minority Populations with Chronic Myeloid Leukemia: A Surveillance Epidemiology and End Results Database Analysis
Published in Blood (29-11-2018)“…Introduction: Cancer affects people of all races in the U.S.; however, the burden is greater for minority populations. This is influenced by factors such as…”
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