Hassell, Kathryn L.

Management of Sickle Cell Disease: Summary of the 2014 Evidence-Based Report by Expert Panel Members

Yawn, B. P., Buchanan, G. R., Afenyi-Annan, A. N., Ballas, S. K., Hassell, K. L., James, A. H., Jordan, L., Lanzkron, S. M., Lottenberg, R., Savage, W. J., et al. (2014) · JAMA

Hemoglobinopathies and Related DisordersHemophilia Treatment and Research

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Echocardiographic Markers of Elevated Pulmonary Pressure and Left Ventricular Diastolic Dysfunction Are Associated With Exercise Intolerance in Adults and Adolescents With Homozygous Sickle Cell Anemia in the United States and United Kingdom

Sachdev, V., Kato, G. J., Gibbs, J. S. R., Barst, R. J., Machado, R. F., Nouraie, M., Hassell, K. L., Little, J. A., Schraufnagel, D. E., Krishnamurti, L., et al. (2011) · Circulation

Hemoglobinopathies and Related DisordersPulmonary Hypertension Research and Treatments

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Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom

Gladwin, M. T., Barst, R. J., Gibbs, J. S. R., Hildesheim, M., Sachdev, V., Nouraie, M., Hassell, K. L., Little, J. A., Schraufnagel, D. E., Krishnamurti, L., et al. (2014) · PLoS ONE

Hemoglobinopathies and Related DisordersPulmonary Hypertension Research and Treatments

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Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks

Keller, S. D., Yang, M., Treadwell, M. J., Werner, E. M., & Hassell, K. L. (2014) · Health and Quality of Life Outcomes

Hemoglobinopathies and Related DisordersHealth Education and Validation

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Effects of hydroxyurea treatment for patients with hemoglobin SC disease

Luchtman‐Jones, L., Pressel, S., Hilliard, L., Brown, R. C., Smith, M. G., Thompson, A. A., Lee, M. T., Rothman, J., Rogers, Z. R., Owen, W., et al. (2016) · American Journal of Hematology

Hemoglobinopathies and Related DisordersHemophilia Treatment and Research

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