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Authors whose works are in public domain in at least one jurisdiction

List of works by Michele Lloyd-Puryear

A Public Health Framework for Rare Blood Disorders

scientific article published on December 1, 2011

A Roadmap to Newborn Screening for Duchenne Muscular Dystrophy

scientific article published on 07 April 2017

A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: recommendations of the United States secretary for health and human services advisory committee on heritable disorders in newborns a

scientific article published in February 2010

American Academy of Pediatrics Newborn Screening Task Force recommendations: how far have we come?

scientific article published on May 2006

Assessment of newborn screening parent education materials

scientific article published on 01 May 2006

Assuring clinical genetic services for newborns identified through U.S. newborn screening programs

scientific article published in August 2007

Attitudes about genetics in underserved, culturally diverse populations

scientific article published in January 2005

Carrier testing for spinal muscular atrophy

scientific article

Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review

scientific article published on 30 October 2018

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project

scientific article published in March 2011

Committee Report: advancing the current recommended panel of conditions for newborn screening

scientific article

Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children

scientific article published on March 2010

Correction: Regional models of genetic services in the United States

scientific article published on 01 January 2020

Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations

scientific article published on 25 January 2018

Duchenne Muscular Dystrophy Newborn Screening: Evaluation of a New GSP® Neonatal Creatine Kinase-MM Kit in a US and Danish Population

scientific article published on 27 August 2019

Educational needs in genetic medicine: primary care perspectives

scientific article

Empowering newborn screening programs in African countries through establishment of an international collaborative effort

scientific article published on 15 May 2020

Enhancing communication in the 21st century

scientific article published on 01 May 2006

Enhancing the quality and efficiency of newborn screening programs through the use of health information technology

scientific article published on April 2010

Evolution of a child health profile initiative

scientific article published on 01 November 2004

Examination of the communication practices between state newborn screening programs and the medical home

scientific article published on February 2003

Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism

scientific article

Financing newborn screening: sources, issues, and future considerations

scientific article published on March 2007

Financing state newborn screening programs: sources and uses of funds

scientific article published on 01 May 2006

Foundation of the Newborn Screening Translational Research Network and its tools for research

scientific article published on 05 November 2018

Fred Lorey Passed Away

scientific article published on 04 November 2020

From developing guidelines to implementing legislation: actions of the US Advisory Committee on Heritable Disorders in Newborns and Children toward advancing and improving newborn screening

scientific article published on 01 April 2010

Future research directions to identify causes of the increasing incidence rate of congenital hypothyroidism in the United States

scientific article published on May 2010

Genetics in primary care: a USA faculty development initiative

scientific article published on 01 January 2002

Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative

scientific article

Healthy choices through family history: a community approach to family history awareness

scientific article published on 5 August 2008

Improving newborn screening follow-up in pediatric practices: quality improvement innovation network

scientific article published on 6 August 2012

Inborn errors of metabolism identified via newborn screening: Ten-year incidence data and costs of nutritional interventions for research agenda planning

scientific article

Including ELSI research questions in newborn screening pilot studies

scientific article published on 13 August 2018

Insurance coverage of medical foods for treatment of inherited metabolic disorders

scientific article published on April 18, 2013

Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children

scientific article published on 01 April 2008

Long-term follow-up in newborn screening: A systems approach for improving health outcomes

scientific article published on December 1, 2010

Long-term follow-up of newborn screening patients

scientific article published on December 2010

Long-term outcomes of the "Genetics in Primary Care" faculty development initiative

scientific article published on 01 April 2009

Main Report

scientific article published in May 2006

Medical foods: inborn errors of metabolism and the reimbursement dilemma

scientific article published on June 2010

Models of comprehensive multidisciplinary care for individuals in the United States with genetic disorders.

scientific article published on January 2009

Naming and counting disorders (conditions) included in newborn screening panels

scientific article published in May 2006

Newborn screening and genetic testing

scientific article

Newborn screening for Pompe disease: synthesis of the evidence and development of screening recommendations

scientific article published on November 2007

Newborn screening for sickle cell diseases in the United States: A review of data spanning 2 decades

scientific article

Newborn screening: toward a uniform screening panel and system

scientific article (publication date: May 2006)

Nutritional treatment for inborn errors of metabolism: Indications, regulations, and availability of medical foods and dietary supplements using phenylketonuria as an example

scientific article published on July 16, 2012

Personalizing prenatal care using family health history: identifying a panel of conditions for a novel electronic genetic screening tool

scientific article published on 01 May 2013

Phenylketonuria Scientific Review Conference: state of the science and future research needs

scientific article published on 6 March 2014

Public health implications of sickle cell trait: a report of the CDC meeting

scientific article published in December 2011

Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts

scientific article published on 01 May 2006

Regional models of genetic services in the United States

scientific article published on 06 September 2019

Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy

scientific article published on May 29, 2013

Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: The changing moral focus of newborn screening

scientific article published on April 1, 2011

Sickle cell disease: the need for a public health agenda

scientific article published on December 2011

Standardizing newborn screening results for health information exchange.

scientific article

The near-term future for child health information systems

scientific article

The regional genetic and newborn screening service collaboratives: the first two years

scientific article published on 01 January 2006

Understanding newborn screening system issues with emphasis on cystic fibrosis screening

scientific article