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Adult phenylketonuria

The American journal of medicine, 2004-10, Vol.117 (8), p.590-595

Hanley, W.B.

2004

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Non-PKU mild hyperphenylalaninemia (MHP) — The dilemma

Molecular genetics and metabolism, 2011-09, Vol.104 (1-2), p.23-26

Hanley, W.B.

2011

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False-positive results in expanded newborn screening

Pediatrics (Evanston), 2007-02, Vol.119 (2), p.414

Hanley, W B

2007

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Congenital heart disease in Maternal phenylketonuria: Report from the Maternal PKU Collaborative study

Pediatric research, 2001-05, Vol.49 (5), p.636-642

2001

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The International Study of Pregnancy Outcome in Women with Maternal Phenylketonuria: Report of a 12-year study

American journal of obstetrics and gynecology, 2000-02, Vol.182 (2), p.326-333

2000

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Phenylalanine hydroxylase gene mutations in the United States : Report from the maternal PKU collaborative study

American journal of human genetics, 1996-07, Vol.59 (1), p.84-94

1996

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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

1999

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Maternal Phenylketonuria Collaborative Study (MPKUCS)—The 'outliers'

Journal of inherited metabolic disease, 2004-01, Vol.27 (6), p.711-723

2004

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The efficacy of stethoscope placement when not in use: traditional versus "cool"

Canadian Medical Association journal, 2000-12, Vol.163 (12), p.1562

2000

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“Hypotyrosinemia” in Phenylketonuria

Molecular genetics and metabolism, 2000-04, Vol.69 (4), p.286-294

2000

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Phenylketonuria: questioning the gospel

Expert Review of Endocrinology & Metabolism, 2007-11, Vol.2 (6), p.809-816

Hanley, W B

2007

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Randomised controlled trial of tyrosine supplementation on neuropsychological performance in phenylketonuria

Archives of disease in childhood, 1998-02, Vol.78 (2), p.116-121

1998

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Undiagnosed maternal phenylketonuria: The need for prenatal selective screening or case finding

American journal of obstetrics and gynecology, 1999-04, Vol.180 (4), p.986-994

1999

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Newborn phenylketonuria (PKU) Guthrie (BIA) screening and early hospital discharge

Early human development, 1997-01, Vol.47 (1), p.87-96

1997

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Maternal phenylketonuria collaborative study, obstetric aspects and outcome: The first 6 years

American journal of obstetrics and gynecology, 1992-04, Vol.166 (4), p.1150-1162

1992

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Feto-maternal plasma phenylalanine concentration gradient from 19 weeks gestation to term

Clinica chimica acta, 1994-03, Vol.225 (2), p.165-169

1994

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Low iron stores in infants and children with treated phenylketonuria : a population at risk for iron-deficiency anaemia and associated cognitive deficits

European journal of pediatrics, 1993-02, Vol.152 (2), p.140-143

1993

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Maternal PKU Collaborative Study: Pregnancy outcome and postnatal head growth

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.353-355

1994

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The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary report

European journal of pediatrics, 1996-07, Vol.155 Suppl 1 (S1), p.S169-S172

1996

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Maternal phenylketonuria (PKU) — A review

Clinical biochemistry, 1987-06, Vol.20 (3), p.149-156

1987

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Maternal non-phenylketonuric mild hyperphenylalaninemia

European journal of pediatrics, 1996-07, Vol.155 Suppl 1 (S1), p.S20-S25

1996

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Biopterin synthesis defect: treatment with L-dopa and 5-hydroxytryptophan compared with therapy with a tetrahydropterin

The Journal of clinical investigation, 1984-02, Vol.73 (2), p.458-469

1984

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Undiagnosed phenylketonuria in adult women: a hidden public health problem

Canadian Medical Association journal (CMAJ), 1990-09, Vol.143 (6), p.513

1990

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Phenylketonuria and its variants: observations on intellectual functioning

Canadian Medical Association journal, 1984-10, Vol.131 (7), p.751-755

1984

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A test of the frontal-specificity hypothesis in the cognitive performance of adults with phenylketonuria

Developmental neuropsychology, 1996-01, Vol.12 (3), p.327-341

1996

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Adult phenylketonuria

Non-PKU mild hyperphenylalaninemia (MHP) — The dilemma

False-positive results in expanded newborn screening

Congenital heart disease in Maternal phenylketonuria: Report from the Maternal PKU Collaborative study

The International Study of Pregnancy Outcome in Women with Maternal Phenylketonuria: Report of a 12-year study

Phenylalanine hydroxylase gene mutations in the United States : Report from the maternal PKU collaborative study

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

Maternal Phenylketonuria Collaborative Study (MPKUCS)—The 'outliers'

The efficacy of stethoscope placement when not in use: traditional versus "cool"

“Hypotyrosinemia” in Phenylketonuria

Phenylketonuria: questioning the gospel

Randomised controlled trial of tyrosine supplementation on neuropsychological performance in phenylketonuria

Undiagnosed maternal phenylketonuria: The need for prenatal selective screening or case finding

Newborn phenylketonuria (PKU) Guthrie (BIA) screening and early hospital discharge

Maternal phenylketonuria collaborative study, obstetric aspects and outcome: The first 6 years

Feto-maternal plasma phenylalanine concentration gradient from 19 weeks gestation to term

Low iron stores in infants and children with treated phenylketonuria : a population at risk for iron-deficiency anaemia and associated cognitive deficits

Maternal PKU Collaborative Study: Pregnancy outcome and postnatal head growth

The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary report

Maternal phenylketonuria (PKU) — A review

Maternal non-phenylketonuric mild hyperphenylalaninemia

Biopterin synthesis defect: treatment with L-dopa and 5-hydroxytryptophan compared with therapy with a tetrahydropterin

Undiagnosed phenylketonuria in adult women: a hidden public health problem

Phenylketonuria and its variants: observations on intellectual functioning

A test of the frontal-specificity hypothesis in the cognitive performance of adults with phenylketonuria

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