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Ethical Issues Surrounding Newborn Screening

International journal of neonatal screening, 2021-01, Vol.7 (1), p.3

Howell, R Rodney

2021

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The Progress and Future of US Newborn Screening

International journal of neonatal screening, 2022-07, Vol.8 (3), p.41

2022

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A Visit with Dr. Louis Woolf, Recognizing His 100th Birthday and His Contributions to the Diagnosis and Treatment of Phenylketonuria

International journal of neonatal screening, 2020-06, Vol.6 (2), p.45-45

2020

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Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment

World journal of pediatrics : WJP, 2017-06, Vol.13 (3), p.197-201

2017

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We must now put in place an updated, comprehensive newborn screening program for deaf and hard-of-hearing infants

Genetics in medicine, 2019-11, Vol.21 (11), p.2439-2441

Howell, R Rodney

2019

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From a Single Child to Uniform Newborn Screening: My Lucky Life in Pediatric Medical Genetics

Annual review of genomics and human genetics, 2018-08, Vol.19 (1), p.1-14

Howell, R. Rodney

2018

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MOVR-NeuroMuscular ObserVational Research, a unified data hub for neuromuscular diseases

Genetics in medicine, 2019-03, Vol.21 (3), p.536-538

2019

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Strategies for implementing screening for critical congenital heart disease

Pediatrics (Evanston), 2011-11, Vol.128 (5), p.e1259

2011

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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

International journal of neonatal screening, 2018-03, Vol.4 (1), p.6-6

2018

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Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening

Journal of neuromuscular diseases, 2018, Vol.5 (2), p.145-158

2018

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Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2

Journal of neuromuscular diseases, 2020-01, Vol.7 (2), p.97-100

2020

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Fifty years of newborn screening

Molecular genetics and metabolism, 2014-09, Vol.113 (1-2), p.4-5

Howell, R. Rodney

2014

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Whole‐genome sequencing holds the key to the success of gene‐targeted therapies

American journal of medical genetics. Part C, Seminars in medical genetics, 2023-03, Vol.193 (1), p.19-29

2023

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Newborn Screening for Krabbe Disease: A Model of Cooperation

Pediatric neurology, 2009-04, Vol.40 (4), p.256-257

Howell, R. Rodney, MD

2009

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Pompe disease in infants and children

The Journal of pediatrics, 2004-05, Vol.144 (5), p.S35-S43

2004

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Including ELSI research questions in newborn screening pilot studies

Genetics in medicine, 2019-03, Vol.21 (3), p.525-533

2019

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Challenges in drug development for muscle disease: A stakeholders' meeting

Muscle & Nerve, 2007-01, Vol.35 (1), p.8-16

2007

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Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy

The Journal of pediatrics, 2019-01, Vol.204, p.305-313.e14

2019

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Pompe disease diagnosis and management guideline

Genetics in medicine, 2006-05, Vol.8 (5), p.267-288

2006

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CDC Grand Rounds: Newborn Screening and Improved Outcomes

MMWR. Morbidity and mortality weekly report, 2012-06, Vol.61 (21), p.390-393

2012

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Appropriateness of Newborn Screening for α1‐Antitrypsin Deficiency

Journal of pediatric gastroenterology and nutrition, 2014-02, Vol.58 (2), p.199-203

2014

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Quality improvement of newborn screening in real time

Genetics in medicine, 2011-03, Vol.13 (3), p.205-205

Howell, R Rodney

2011

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Every Child Is Priceless: Debating Effective Newborn Screening Policy

The Hastings Center report, 2009-01, Vol.39 (1), p.4-8

2009

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We need expanded newborn screening

Pediatrics (Evanston), 2006-05, Vol.117 (5), p.1800

Howell, R Rodney

2006

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

Genetics in medicine, 2010-03, Vol.12 (3), p.153-159

2010

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Ethical Issues Surrounding Newborn Screening

The Progress and Future of US Newborn Screening

A Visit with Dr. Louis Woolf, Recognizing His 100th Birthday and His Contributions to the Diagnosis and Treatment of Phenylketonuria

Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment

We must now put in place an updated, comprehensive newborn screening program for deaf and hard-of-hearing infants

From a Single Child to Uniform Newborn Screening: My Lucky Life in Pediatric Medical Genetics

MOVR-NeuroMuscular ObserVational Research, a unified data hub for neuromuscular diseases

Strategies for implementing screening for critical congenital heart disease

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

Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening

Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2

Fifty years of newborn screening

Whole‐genome sequencing holds the key to the success of gene‐targeted therapies

Newborn Screening for Krabbe Disease: A Model of Cooperation

Pompe disease in infants and children

Including ELSI research questions in newborn screening pilot studies

Challenges in drug development for muscle disease: A stakeholders' meeting

Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy

Pompe disease diagnosis and management guideline

CDC Grand Rounds: Newborn Screening and Improved Outcomes

Appropriateness of Newborn Screening for α1‐Antitrypsin Deficiency

Quality improvement of newborn screening in real time

Every Child Is Priceless: Debating Effective Newborn Screening Policy

We need expanded newborn screening

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

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