Fred Lorey Passed Away von Feuchtbaum, Lisa, A. Lloyd-Puryear, Michele

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Inborn errors of metabolism identified via newborn screening: Ten-year incidence data and costs of nutritional interventions for research agenda planning von Therrell, Bradford L., Lloyd-Puryear, Michele A., Camp, Kathryn M., Mann, Marie Y.

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The Progress and Future of US Newborn Screening von Watson, Michael S, Lloyd-Puryear, Michele A, Howell, R Rodney

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Nutritional treatment for inborn errors of metabolism: Indications, regulations, and availability of medical foods and dietary supplements using phenylketonuria as an example von Camp, Kathryn M., Lloyd-Puryear, Michele A., Huntington, Kathleen L.

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Newborn screening for sickle cell diseases in the United States: A review of data spanning 2 decades von Therrell, Bradford L., PhD, Lloyd-Puryear, Michele A., MD, PhD, Eckman, James R., MD, Mann, Marie Y., MD, MPH

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Newborn Screening for Six Primary Conditions in a Clinical Setting in Morocco von El Janahi, Sara, Filali, Mounir, Boudar, Zakia, Akhattab, Amina, El Jaoudi, Rachid, Al Idrissi, Najib, Dini, Nouzha, Nejjari, Chakib, Yahyaoui, Raquel, Lloyd-Puryear, Michele A, Ghazal, Hassan

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Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot von Hartnett, Michael J, Lloyd-Puryear, Michele A, Tavakoli, Norma P, Wynn, Julia, Koval-Burt, Carrie L, Gruber, Dorota, Trotter, Tracy, Caggana, Michele, Chung, Wendy K, Armstrong, Niki, Brower, Amy M

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Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations von Lloyd-Puryear, Michele, Crawford, Thomas, Brower, Amy, Stephenson, Kristin, Trotter, Tracy, Goldman, Edward, Goldenberg, Aaron, Howell, R., Kennedy, Annie, Watson, Michael

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A Public Health Framework for Rare Blood Disorders von Grosse, Scott D., PhD, James, Andra H., MD, Lloyd-Puryear, Michele A., MD, PhD, Atrash, Hani K., MD, MPH

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Models of Comprehensive Multidisciplinary Care for Individuals in the United States With Genetic Disorders von Grosse, Scott D, Schechter, Michael S, Kulkarni, Roshni, Lloyd-Puryear, Michele A, Strickland, Bonnie, Trevathan, Edwin

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Considerations for policymakers for improving health care through telegenetics: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG) von Williams, Heather E., Aiyar, Lila, Dinulos, Mary Beth, Flannery, David, McClure, Michelle L., Lloyd-Puryear, Michele A., Sanghavi, Kunal, Trotter, Tracy L., Viskochil, David

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Enhancing the Quality and Efficiency of Newborn Screening Programs Through the Use of Health Information Technology von Downing, Gregory J., DO, PhD, Zuckerman, Alan E., MD, Coon, Constanze, PhD, Lloyd-Puryear, Michele A., MD, PhD

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Newborn screening: toward a uniform screening panel and system--executive summary von Watson, Michael S., Mann, Marie Y., Lloyd-Puryear, Michele A., Rinaldo, Piero, Howell, R. Rodney

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Empowering newborn screening programs in African countries through establishment of an international collaborative effort von Therrell, Bradford L., Lloyd-Puryear, Michele A., Ohene-Frempong, Kwaku, Ware, Russell E., Padilla, Carmencita D., Ambrose, Emmanuela E., Barkat, Amina, Ghazal, Hassan, Kiyaga, Charles, Mvalo, Tisungane, Nnodu, Obiageli, Ouldim, Karim, Rahimy, Mohamed Chérif, Santos, Brígida, Tshilolo, Léon, Yusuf, Careema, Zarbalian, Guisou, Watson, Michael S.

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Sickle cell disease: the need for a public health agenda von Yusuf, Hussain R, Lloyd-Puryear, Michele A, Grant, Althea M, Parker, Christopher S, Creary, Melissa S, Atrash, Hani K

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Public health implications of sickle cell trait: a report of the CDC meeting von Grant, Althea M, Parker, Christopher S, Jordan, Lanetta B, Hulihan, Mary M, Creary, Melissa S, Lloyd-Puryear, Michele A, Goldsmith, Jonathan C, Atrash, Hani K

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Future Research Directions to Identify Causes of the Increasing Incidence Rate of Congenital Hypothyroidism in the United States von SHAPIRA, Stuart K, LLOYD-PURYEAR, Michele A, BOYLE, Coleen

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Insurance coverage of medical foods for treatment of inherited metabolic disorders von Berry, Susan A., Kenney, Mary Kay, Harris, Katharine B., Singh, Rani H., Cameron, Cynthia A., Kraszewski, Jennifer N., Levy-Fisch, Jill, Shuger, Jill F., Greene, Carol L., Lloyd-Puryear, Michele A., Boyle, Coleen A.

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Long-term follow-up in newborn screening: A systems approach for improving health outcomes von Lloyd-Puryear, Michele A., Brower, Amy

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Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism von Camp, Kathryn M., Lloyd-Puryear, Michele A., Yao, Lynne, Groft, Stephen C., Parisi, Melissa A., Mulberg, Andrew, Gopal-Srivastava, Rashmi, Cederbaum, Stephen, Enns, Gregory M., Ershow, Abby G., Frazier, Dianne M., Gohagan, John, Harding, Cary, Howell, R. Rodney, Regan, Karen, Stacpoole, Peter W., Venditti, Charles, Vockley, Jerry, Watson, Michael, Coates, Paul M.

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