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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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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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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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Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study

Pediatrics (Evanston), 1999-08, Vol.104 (2 Pt 1), p.258-262

1999

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Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome

Pediatrics (Evanston), 2003-12, Vol.112 (6 Pt 2), p.1530

2003

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Challenging the Current Recommendations for Carrier Testing in Children

Pediatrics (Evanston), 2019-01, Vol.143 (Suppl 1), p.S27-S32

2019

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Newborn screening: toward a uniform screening panel and system--executive summary

Pediatrics (Evanston), 2006-05, Vol.117 (5 Pt 2), p.S296-S307

2006

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The Maternal Phenylketonuria International Study: 1984-2002

Pediatrics (Evanston), 2003-12, Vol.112 (6 Pt 2), p.1523

2003

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Historical Background for the Maternal PKU Syndrome

Pediatrics (Evanston), 2003-12, Vol.112 (Supplement_4), p.1516-1518

Levy, Harvey L.

2003

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One more thought on sudden infant death syndrome

Pediatrics (Evanston), 2001-04, Vol.107 (4), p.809-809

2001

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Research design, organization, and sample characteristics of the Maternal PKU Collaborative Study

Pediatrics (Evanston), 2003-12, Vol.112 (6 Pt 2), p.1519

2003

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Impact of the Phenylalanine Hydroxylase Gene on Maternal Phenylketonuria Outcome

Pediatrics (Evanston), 2003-12, Vol.112 (Supplement_4), p.1530-1533

2003

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Pregnancy Experiences in the Woman With Mild Hyperphenylalaninemia

Pediatrics (Evanston), 2003-12, Vol.112 (Supplement_4), p.1548-1552

2003

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Research Design, Organization, and Sample Characteristics of the Maternal PKU Collaborative Study

Pediatrics (Evanston), 2003-12, Vol.112 (Supplement_4), p.1519-1522

2003

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The Maternal Phenylketonuria International Study: 1984–2002

Pediatrics (Evanston), 2003-12, Vol.112 (Supplement_4), p.1523-1529

2003

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Massachusetts Metabolic Disorders Screening Program: III. Sarcosinemia

Pediatrics (Evanston), 1984-10, Vol.74 (4), p.509-513

1984

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Detection of phenylketonuria in the very early newborn blood specimen

Pediatrics (Evanston), 1991-02, Vol.87 (2), p.240-244

1991

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Predictors of intelligence quotient and intelligence quotient change in persons treated for phenylketonuria early in life

Pediatrics (Evanston), 1987-03, Vol.79 (3), p.351-355

1987

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Parental response to repeat testing of infants with 'false-positive' results in a newborn screening program

Pediatrics (Evanston), 1984-02, Vol.73 (2), p.183-187

1984

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Regulation of Amino Acid Metabolism in Mammals, by Bernard Schepartz, Ph.D. Philadelphia/London/Toronto: W. B. Saunders Company, 1973, 205 pp., $9.50

Pediatrics (Evanston), 1974-07, Vol.54 (1), p.128-128

Levy, Harvey L.

1974

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Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria

Pediatrics (Evanston), 1981-01, Vol.67 (1), p.26-31

1981

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Regional newborn screening for hypothyroidism

Pediatrics (Evanston), 1979-02, Vol.63 (2), p.340-342

1979

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Massachusetts metabolic disorders screening program. I. Technics and results of urine screening

Pediatrics (Evanston), 1972-06, Vol.49 (6), p.825-836

1972

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Historical background for the maternal PKU syndrome

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

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

Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study

Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome

Challenging the Current Recommendations for Carrier Testing in Children

Newborn screening: toward a uniform screening panel and system--executive summary

The Maternal Phenylketonuria International Study: 1984-2002

Historical Background for the Maternal PKU Syndrome

One more thought on sudden infant death syndrome

Research design, organization, and sample characteristics of the Maternal PKU Collaborative Study

Impact of the Phenylalanine Hydroxylase Gene on Maternal Phenylketonuria Outcome

Pregnancy Experiences in the Woman With Mild Hyperphenylalaninemia

Research Design, Organization, and Sample Characteristics of the Maternal PKU Collaborative Study

The Maternal Phenylketonuria International Study: 1984–2002

Massachusetts Metabolic Disorders Screening Program: III. Sarcosinemia

Detection of phenylketonuria in the very early newborn blood specimen

Predictors of intelligence quotient and intelligence quotient change in persons treated for phenylketonuria early in life

Parental response to repeat testing of infants with 'false-positive' results in a newborn screening program

Regulation of Amino Acid Metabolism in Mammals, by Bernard Schepartz, Ph.D. Philadelphia/London/Toronto: W. B. Saunders Company, 1973, 205 pp., $9.50

Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria

Regional newborn screening for hypothyroidism

Massachusetts metabolic disorders screening program. I. Technics and results of urine screening

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