Search Results - "Dulman, Robin"
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A randomized trial of the effectiveness of the neutropenic diet versus food safety guidelines on infection rate in pediatric oncology patients
Published in Pediatric blood & cancer (01-01-2018)“…Background The neutropenic diet (ND) is prescribed to avoid introduction of bacteria into a host's gastrointestinal tract and reduce infection. Due to a lack…”
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LNK/ SH2B3 as a novel driver in juvenile myelomonocytic leukemia
Published in Haematologica (Roma) (28-12-2023)“…Mutations in five canonical Ras pathway genes (NF1, NRAS, KRAS, PTPN11 and CBL) are detected in nearly 90% of patients with juvenile myelomonocytic leukemia…”
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3
Lung Opacification
Published in JAMA : the journal of the American Medical Association (18-06-2014)“…Teo et al talks about a case of a 16-year-old girl, who presents with acute left shoulder pain, left-sided chest pain, and shortness of breath, with a history…”
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High Hydroxyurea Usage in Sickle Cell Anemia Regardless of Patient Demographic
Published in Blood (02-11-2023)“…Introduction/Background: Hydroxyurea is highly effective in sickle cell disease, yet it is still underutilized. The Pediatric Sickle Cell Program of Northern…”
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High hydroxyurea usage in sickle cell anemia regardless of patient demographics
Published in Pediatric blood & cancer (01-02-2024)“…Hydroxyurea is highly effective in sickle cell disease, but it is still underutilized. Reports of hydroxyurea utilization largely use Medicaid data, and…”
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Prospective longitudinal follow‐up of children with sickle cell disease treated with hydroxyurea since infancy
Published in Pediatric blood & cancer (01-09-2019)“…Background Hydroxyurea (HU) increases fetal hemoglobin (HgbF) and ameliorates sickle cell disease (SCD) symptoms. Studies have demonstrated the safety and…”
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Ten‐year longitudinal analysis of hydroxyurea implementation in a pediatric sickle cell program
Published in European journal of haematology (01-11-2022)“…Hydroxyurea (HU) has proven benefit in sickle cell anemia (SCA), but HU is still underutilized. The Pediatric Sickle Cell Program of Northern Virginia…”
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Outcome of Initiating Hydroxyurea in Infancy for Patients with Sickle Cell Disease 2011-2018
Published in Blood (29-11-2018)“…Introduction Approximately 2000 babies are born with sickle cell disease annually in the US. Children with severe forms of sickle cell disease (SCD), such as…”
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LNK/SH2B3 As a Novel Driver in Juvenile Myelomonocytic Leukemia
Published in Blood (15-11-2022)Get full text
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Effect of voxelotor on cardiopulmonary testing in youths with sickle cell anemia in a pilot study
Published in Pediatric blood & cancer (01-08-2023)“…Background Individuals with sickle cell anemia (SCA) exhibit decreased exercise capacity. Anemia limits oxygen‐carrying capacity and affects cardiopulmonary…”
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The Effect of Voxelotor on Exercise Capacity of Youths with Sickle Cell Anemia
Published in Blood (23-11-2021)“…Background/Hypothesis: Children and adults with sickle cell anemia (SCA) exhibit decreased cardiopulmonary fitness. Anemia is directly related to oxygen…”
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Robust immune responses to SARS-CoV-2 in a pediatric patient with B-Cell ALL receiving tisagenlecleucel
Published in Pediatric hematology and oncology (18-08-2022)“…Recipients of anti-CD19 targeted therapies such as chimeric antigen receptor (CAR)-T cell are considered at high risk for complicated Severe Acute Respiratory…”
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Discontinuation of Folic Acid Supplementation in Young Patients With Sickle Cell Anemia
Published in Journal of pediatric hematology/oncology (01-08-2017)“…Folic acid (FA) is commonly prescribed for patients with sickle cell anemia, but evidence for the efficacy of this practice is lacking. We stopped FA…”
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Wild type N-ras displays anti-malignant properties, in part by downregulating decorin
Published in Journal of cellular physiology (01-06-2012)“…Previously, we have shown that wild type N‐ras (wt N‐ras) harbors an anti‐malignant effect against mutated Ras and in tumors without Ras mutations. To…”
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Splenic infarction due to concomitant hereditary spherocytosis and sickle cell trait
Published in Journal of pediatric surgery (01-12-2007)“…Abstract Concomitant hereditary spherocytosis and sickle cell trait, although extremely rare, could potentially lead to splenic sequestration or infarction. We…”
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