Professor, Pediatrics, University of Missouri, Kansas City School of Medicine Division Director, Children's Mercy Hospital, Kansas City, Missouri
Pediatric Hematology & Oncology
Dr. Gerald M. Woods, MD
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Gerald Woods works in the field of Pediatric Hematology & Oncology. He attended Duke University School of Medicine. Duke University School of Medicine is one of the top medical schools in the US. Duke University School of Medicine has a rank of 8 in research and a 29 in primary care He over the years received 3 awards: "Regional Top Doctor", "Fellow (FAAP)" and "Super Doctor". Gerald Woods has written publications. He has 40 publications published with PubMed. The lastest paper is: 'Influence of penicillin prophylaxis on antimicrobial resistance in nasopharyngeal S. pneumoniae among children with sickle cell anemia. The Ancillary Nasopharyngeal Cu...'
Publications
- Controlled trial of transfusions for silent cerebral infarcts in sickle cell Anemia.
- Silent cerebral infarction, income and grade retention among students with Sickle cell.
- Practice Patterns of Stroke Screening and Hydroxyurea Use in Children With Sickle Cell Disease: A Survey of Health Care Providers.
- Associated risk factors for silent cerebral infarcts in sickle cell Anemia: low baseline hemoglobin, gender and relative high systolic blood pressure.
- Oxidant-mediated modification of the Cellular thiols is sufficient for arginase activation in cultured Cells.
- Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with Sickle cell disease.
- Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic Anemia mouse model.
- Serum ferritin level changes in children with Sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
- A colorimetric microplate assay method for high-throughput analysis of arginase activity in vitro.
- Cysteine-iron promotes arginase activity by driving the Fenton reaction.
- Severe pulmonary hypertension in an adolescent with Sickle cell disease.
- Disseminated nontuberculous mycobacterial infections in sickle cell Anemia patients.
- Quality of life among children with Sickle cell disease receiving chronic transfusion therapy.
- Risk of recurrent stroke in children with Sickle cell disease receiving blood transfusion therapy for at least five years after initial stroke.
- Modification of the Shandon Southern apparatus MK II for SDS preparative polyacrylamide gel electrophoresis.
- Lennert''s Lymphoma: response to 2''-deoxycoformycin.
- X;6 translocation in a child with congenital Acute lymphocytic leukemia.
- Diffuse bony metastases at presentation in a child with glioblastoma multiforme. A case report.
- Pancreatoduodenectomy for neonatal myofibromatosis of the pancreas.
- Alpha-streptococcal septicemia in leukemic children treated with continuous or large dosage intermittent cytosine arabinoside.
- Ketorolac-induced irreversible Renal failure in sickle cell disease: a case report.
- Absence of one component of spectrin adenosine triphosphatase in hereditary spherocytosis.
- Functional asplenia in hemoglobin SC Disease.
- Fatal pneumococcal septicemia in hemoglobin SC Disease.
- A chronology of pain and comfort in children with Sickle cell disease.
- Efficacy of nalbuphine as a parenteral analgesic for the treatment of painful episodes in children with Sickle cell disease.
- Exchange blood transfusion compared with simple transfusion for first overt stroke is associated with a lower risk of subsequent stroke: a retrospective cohort study o...
- Growth inhibitory and differentiation effects of chloroquine and its analogue on human leukemic Cells potentiate fetal hemoglobin production by targeting the polyamine...
- Dysfunctional eating patterns and symptoms of pica in children and adolescents with Sickle cell disease.
- Serotype-specific immunoglobulin G antibody responses to pneumococcal polysaccharide vaccine in children with sickle cell Anemia: effects of continued penicillin proph...
- Can peak systolic velocities be used for prediction of stroke in sickle cell Anemia?
- Discontinuing penicillin prophylaxis in children with sickle cell Anemia. Prophylactic Penicillin Study II.
- Influence of penicillin prophylaxis on antimicrobial resistance in nasopharyngeal S. pneumoniae among children with sickle cell Anemia. The Ancillary Nasopharyngeal Cu...
- Magnetic resonance angiography in children with Sickle cell disease and abnormal transcranial Doppler ultrasonography findings enrolled in the STOP study.
- Modulation of erythrocyte arginase activity in Sickle cell disease patients during hydroxyurea therapy.
- Alpha Thalassemia is associated with decreased risk of abnormal transcranial Doppler ultrasonography in children with sickle cell Anemia.
- Stroke and conversion to high risk in children screened with transcranial Doppler ultrasound during the STOP study.
- The impact of parenteral narcotic choice in the development of Acute chest syndrome in sickle cell disease.
- In vitro evidence of the inhibitory capacity of chloroquine on arginase activity in Sickle erythrocytes.
Schools
Duke University
Chldns Mercy Hospital
Duke University Med Center
Conditions Treated
- Acute Leukemia
- Anemia
- Brain and Nervous System Cancer (incl. Gliomas, Astrocytoma, Schwannoma, Medulloblastoma, Chordoma)
- Brain Cancer
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Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
Awards
- Regional Top Doctor
- Fellow (FAAP)
- Super Doctor
Education
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Duke University Hospital -
Duke University School of Medicine
Hospital
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Children's Mercy Hospitals and Clinics
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