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Can Newborn Screening for Vitamin B 12 Deficiency be Incorporated into All Newborn Screening Programs?

The Journal of pediatrics, 2020-01, Vol.216, p.9

2020

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Robert Guthrie and the Trials and Tribulations of Newborn Screening

International journal of neonatal screening, 2021-01, Vol.7 (1), p.5

Levy, Harvey L

2021

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Early Development of Newborn Screening for HCU and Current Challenges

International journal of neonatal screening, 2021-10, Vol.7 (4), p.67

Levy, Harvey L.

2021

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Ethical and Psychosocial Implications of Genomic Newborn Screening

International journal of neonatal screening, 2021-01, Vol.7 (1), p.2

Levy, Harvey L

2021

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The BabySeq project: implementing genomic sequencing in newborns

BMC pediatrics, 2018-07, Vol.18 (1), p.225-225, Article 225

2018

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Past as Prologue: Predicting Potential Psychosocial-Ethical Burdens of Positive Newborn Screens as Conditions Propagate

International journal of neonatal screening, 2024-02, Vol.10 (1), p.12

2024

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Genomics in Newborn Screening

The Journal of pediatrics, 2014, Vol.164 (1), p.14-19

2014

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Long-term outcome of expanded newborn screening at Boston children’s hospital: benefits and challenges in defining true disease

Journal of inherited metabolic disease, 2017-03, Vol.40 (2), p.209-218

2017

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Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project

Genetics in medicine, 2019-03, Vol.21 (3), p.622-630

2019

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A Life in Newborn Screening

International journal of neonatal screening, 2016-12, Vol.2 (4), p.14

Levy, Harvey

2016

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Acute Illness Protocol for Organic Acidemias: Methylmalonic Acidemia and Propionic Acidemia

Pediatric emergency care, 2017-02, Vol.33 (2), p.142-146

2017

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Acute Illness Protocol for Maple Syrup Urine Disease

Pediatric emergency care, 2018-01, Vol.34 (1), p.64-67

2018

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Newborn screening for metabolic disorders

The Journal of pediatrics, 2006-05, Vol.148 (5), p.577-584.e5

2006

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Is Melatonin Synthesis a New Biomarker for the Pathogenesis and Treatment of Phenylketonuria?

The Journal of pediatrics, 2013-05, Vol.162 (5), p.893-894

2013

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Acute Illness Protocol for Urea Cycle Disorders

Pediatric emergency care, 2018-06, Vol.34 (6), p.e115-e119

2018

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Acute Illness Protocol for Fatty Acid Oxidation and Carnitine Disorders

Pediatric emergency care, 2017-04, Vol.33 (4), p.296-301

2017

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Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn Screening

International journal of neonatal screening, 2021-09, Vol.7 (3), p.48

2021

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Historical background for the maternal PKU syndrome

Pediatrics (Evanston), 2003-12, Vol.112 (6 Pt 2), p.1516

Levy, Harvey L

2003

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Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria

Genetics in medicine, 2019-08, Vol.21 (8), p.1851-1867

2019

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Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

JAMA pediatrics, 2021-11, Vol.175 (11), p.1132

2021

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Detection of neonatal carnitine palmitoyltransferase II deficiency by expanded newborn screening with tandem mass spectrometry

Pediatrics (Evanston), 2001-06, Vol.107 (6), p.E103-e103

2001

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Krabbe Disease: Severe Neonatal Presentation With a Family History of Multiple Sclerosis

Journal of child neurology, 2005-10, Vol.20 (10), p.826-828

2005

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Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project

Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S6-S13

2019

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Pregnancy experiences in the woman with mild hyperphenylalaninemia

Pediatrics (Evanston), 2003-12, Vol.112 (6 Pt 2), p.1548

2003

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Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project

Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S37-S43

2019

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Can Newborn Screening for Vitamin B 12 Deficiency be Incorporated into All Newborn Screening Programs?

Robert Guthrie and the Trials and Tribulations of Newborn Screening

Early Development of Newborn Screening for HCU and Current Challenges

Ethical and Psychosocial Implications of Genomic Newborn Screening

The BabySeq project: implementing genomic sequencing in newborns

Past as Prologue: Predicting Potential Psychosocial-Ethical Burdens of Positive Newborn Screens as Conditions Propagate

Genomics in Newborn Screening

Long-term outcome of expanded newborn screening at Boston children’s hospital: benefits and challenges in defining true disease

Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project

A Life in Newborn Screening

Acute Illness Protocol for Organic Acidemias: Methylmalonic Acidemia and Propionic Acidemia

Acute Illness Protocol for Maple Syrup Urine Disease

Newborn screening for metabolic disorders

Is Melatonin Synthesis a New Biomarker for the Pathogenesis and Treatment of Phenylketonuria?

Acute Illness Protocol for Urea Cycle Disorders

Acute Illness Protocol for Fatty Acid Oxidation and Carnitine Disorders

Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn Screening

Historical background for the maternal PKU syndrome

Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial

Detection of neonatal carnitine palmitoyltransferase II deficiency by expanded newborn screening with tandem mass spectrometry

Krabbe Disease: Severe Neonatal Presentation With a Family History of Multiple Sclerosis

Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project

Pregnancy experiences in the woman with mild hyperphenylalaninemia

Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project

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