Professor, Pediatrics, Medical College of Wisconsin
Pediatric Hematology & Oncology
Dr. Julie A. Panepinto, MD
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Julie Panepinto is an expert in the field of Pediatric Hematology & Oncology. Julie Panepinto has written publications. She has 62 publications published with PubMed. The lastest publication is: 'Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease.'
Publications
- Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease.
- A multi-center randomized controlled trial of intravenous magnesium for Sickle cell pain crisis in children.
- Health-related quality of life in children with sickle cell Anemia: impact of blood transfusion therapy.
- A Comparison of Pain Assessment Measures in Pediatric Sickle Cell Disease: Visual Analog Scale Versus Numeric Rating Scale.
- Comparative Effectiveness and Practice Variation in Neonatal Care.
- The Use of Neuropathic Pain Drugs in Children With Sickle Cell Disease is Associated With Older Age, Female Sex, and Longer Length of Hospital Stay.
- Controlled trial of transfusions for silent cerebral infarcts in sickle cell Anemia.
- Silent cerebral infarction, income and grade retention among students with Sickle cell.
- Clinically Meaningful Interpretation of Pediatric Health-related Quality of Life in Sickle Cell Disease.
- The Proportion of Potentially Preventable Emergency Department Visits by Patients With Sickle Cell Disease.
- Intravenous magnesium for pediatric Sickle cell vaso-occlusive crisis: Methodological issues of a randomized controlled trial.
- Clinically meaningful measurement of pain in children with Sickle cell disease.
- Neuropathic pain in patients with Sickle cell disease.
- PedsQL™ multidimensional fatigue scale in Sickle cell disease: Feasibility, reliability, and validity.
- Vitamin B12 deficiency: The great masquerader.
- Academic attainment findings in children with Sickle cell disease.
- Assessment of communication modes in patients and families with Sickle cell disease.
- Severe Thrombocytopenia in a Child Secondary to Passive Platelet Antibody Transfer from a Plasma Transfusion.
- PedsQL™ Sickle Cell Disease Module: Feasibility, Reliability, and Validity.
- Health-related quality of life in patients with hemoglobinopathies.
- Mental health Disorders influence admission rates for pain in children with sickle cell disease.
- Concentration of hospital care for acute Sickle cell disease-related visits.
- Patients with Sickle cell disease have increased sensitivity to cold and heat.
- Health-related quality of life in Sickle cell disease: Past, present, and future.
- Associated risk factors for silent cerebral infarcts in sickle cell Anemia: low baseline hemoglobin, gender and relative high systolic blood pressure.
- Monitoring toxicity, impact, and adherence of hydroxyurea in children with Sickle cell disease.
- When children with Sickle-cell disease become adults: Lack of outpatient care leads to increased use of the emergency department.
- Development of the PedsQL™ Sickle cell disease module items: qualitative methods.
- Differences in health-related quality of life in children with Sickle cell disease receiving hydroxyurea.
- The impact of a multidisciplinary pain management model on Sickle cell disease pain hospitalizations.
- Outpatient follow-up and rehospitalizations for Sickle cell disease patients.
- Silent cerebral infarcts occur despite regular blood transfusion therapy after first strokes in children with Sickle cell disease.
- The effect of parental mental health on proxy reports of health-related quality of life in children with Sickle cell disease.
- Hydroxyurea in children with Sickle cell disease: practice patterns and barriers to utilization.
- Acute care utilization and rehospitalizations for Sickle cell disease.
- The number of people with sickle-cell disease in the United States: national and State estimates.
- Vaso-occlusive painful events in Sickle cell disease: impact on child well-being.
- Dissatisfaction with hospital care for children with Sickle cell disease not due only to race and chronic disease.
- The performance of the PedsQL generic core scales in children with Sickle cell disease.
- Health-related quality of life in Sickle cell disease.
- Parental perception of quality of hospital care for children with Sickle cell disease.
- The effect of acute pain crisis on exhaled nitric oxide levels in children with Sickle cell disease.
- The effect of CYP2D6 polymorphisms on the response to pain treatment for pediatric Sickle cell pain crisis.
- 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...
- Attitudes regarding fertility preservation in female adolescent cancer patients.
- Perioperative management of Sickle cell disease children undergoing adenotonsillectomy.
- Acute idiopathic Thrombocytopenic purpura of childhood-diagnosis and therapy.
- Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in Sickle cell disease.
- The effect of magnesium on length of stay for pediatric Sickle cell pain crisis.
- Validity of the child health questionnaire for use in children with Sickle cell disease.
- Pathophysiology of stroke in Sickle cell disease.
- Hydroxyurea use in Sickle cell disease: the battle with low prescription rates, poor patient compliance and fears of toxicities.
- A psychometric evaluation of the PedsQL Family Impact Module in parents of children with Sickle cell disease.
- Impact of family income and Sickle cell disease on the health-related quality of life of children.
- Postdischarge pain, functional limitations and impact on caregivers of children with Sickle cell disease treated for painful events.
- Matched-related donor transplantation for Sickle cell disease: report from the Center for International Blood and Transplant Research.
- Health-related quality of life in children with Sickle cell disease: child and parent perception.
- Laparoscopic versus open abdominal surgery in children with Sickle cell disease is associated with a shorter hospital stay.
- Improving communication between doctors and parents after newborn screening.
- Universal versus targeted screening of infants for Sickle cell disease: a cost-effectiveness analysis.
- Clinical features of a human Rac2 mutation: a complex neutrophil dysfunction Disease.
Schools
University Of Colorado School Of Medicine
University Wisc Hospital Clin
University Of Wisconsin School Of Medicine and Public Health
University Of Colorado
Conditions Treated
- Anemia
- Antiphospholipid Syndrome (APS)
- Coagulation Disorders (incl. Hemophilia)
- Hypercoagulable State
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Doctors Specialties
- Hematology
- Pediatric Hematology
- Oncology
Accepted Insurances
Education
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University of Colorado -
University of Wisconsin
Hospital
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Children's Hospital of Wisconsin
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