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Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia

Pediatrics (Evanston), 1998-04, Vol.101 (4 Pt 1), p.583-590

1998

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Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

Genetics in medicine, 2011-07, Vol.13 (7), p.621-624

2011

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Newborn screening in the developing countries

Current opinion in pediatrics, 2018-12, Vol.30 (6), p.734-739

2018

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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

Molecular genetics and metabolism, 2014-09, Vol.113 (1-2), p.14-26

2014

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

Seminars in perinatology, 2015-04, Vol.39 (3), p.238-251

2015

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Newborn Screening for Congenital Hypothyroidism in India: Let's Just Do It

Indian pediatrics, 2019-04, Vol.56 (4), p.275-276

Therrell, Jr, Bradford L

2019

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History and Current Status of Newborn Screening for Hemoglobinopathies

Seminars in perinatology, 2010-04, Vol.34 (2), p.134-144

2010

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Immunoreactive trypsinogen (IRT) as a biomarker for cystic fibrosis: Challenges in newborn dried blood spot screening

Molecular genetics and metabolism, 2012-05, Vol.106 (1), p.1-6

2012

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

Journal of community genetics, 2020-07, Vol.11 (3), p.253-268

2020

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Newborn dried blood spot screening: residual specimen storage issues

Pediatrics (Evanston), 2012-02, Vol.129 (2), p.365-366

2012

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Consolidating newborn screening efforts in the Asia Pacific region: Networking and shared education

Journal of community genetics, 2012, Vol.3 (1), p.35-45

2012

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Newborn Screening Progress in Developing Countries—Overcoming Internal Barriers

Seminars in perinatology, 2010-04, Vol.34 (2), p.145-155

2010

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Successful Implementation of Expanded Newborn Screening in the Philippines Using Tandem Mass Spectrometry

International journal of neonatal screening, 2022-01, Vol.8 (1), p.8

2022

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Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines

International journal of neonatal screening, 2021-06, Vol.7 (2), p.30

2021

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Newborn Screening System Performance Evaluation Assessment Scheme (PEAS)

Seminars in perinatology, 2010-04, Vol.34 (2), p.105-120

2010

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Considerations in choosing screening conditions: one (US) approach

Annals of the Academy of Medicine, Singapore, 2008-12, Vol.37 (12 Suppl), p.22-25

Therrell, Jr, Bradford L

2008

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Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study

Journal of genetic counseling, 2013-02, Vol.22 (1), p.108-117

2013

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Financing newborn screening systems: US experience

Annals of the Academy of Medicine, Singapore, 2008-12, Vol.37 (12 Suppl), p.97-94

Therrell, Jr, Bradford L

2008

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Newborn screening: rationale for a comprehensive, fully integrated public health system

Molecular Genetics and Metabolism, 2002-12, Vol.77 (4), p.267-273

2002

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An update on public health newborn screening activities. Introduction

Seminars in perinatology, 2010-04, Vol.34 (2), p.103-104

Therrell, Jr, Bradford L

2010

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Newborn screening for all identifiable disorders with tandem mass spectrometry is cost effective: supporting arguments

Annals of the Academy of Medicine, Singapore, 2008-12, Vol.37 (12 Suppl), p.32-34

2008

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

Genetics in medicine, 2007-08, Vol.9 (8), p.518-527

2007

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Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States—lessons learned

Journal of community genetics, 2011-12, Vol.2 (4), p.191-200

2011

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Data integration and warehousing: coordination between newborn screening and related public health programs

Southeast Asian journal of tropical medicine and public health, 2003, Vol.34 Suppl 3, p.63-68

Therrell, Jr, Bradford L

2003

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Ethical, legal and social issues in newborn screening in the United States

Southeast Asian journal of tropical medicine and public health, 2003, Vol.34 Suppl 3, p.52-58

Therrell, Jr, Bradford L

2003

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Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia

Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening

Newborn screening in the developing countries

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

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

Newborn Screening for Congenital Hypothyroidism in India: Let's Just Do It

History and Current Status of Newborn Screening for Hemoglobinopathies

Immunoreactive trypsinogen (IRT) as a biomarker for cystic fibrosis: Challenges in newborn dried blood spot screening

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

Newborn dried blood spot screening: residual specimen storage issues

Consolidating newborn screening efforts in the Asia Pacific region: Networking and shared education

Newborn Screening Progress in Developing Countries—Overcoming Internal Barriers

Successful Implementation of Expanded Newborn Screening in the Philippines Using Tandem Mass Spectrometry

Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines

Newborn Screening System Performance Evaluation Assessment Scheme (PEAS)

Considerations in choosing screening conditions: one (US) approach

Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study

Financing newborn screening systems: US experience

Newborn screening: rationale for a comprehensive, fully integrated public health system

An update on public health newborn screening activities. Introduction

Newborn screening for all identifiable disorders with tandem mass spectrometry is cost effective: supporting arguments

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

Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States—lessons learned

Data integration and warehousing: coordination between newborn screening and related public health programs

Ethical, legal and social issues in newborn screening in the United States

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