Every pediatrician a geneticist (1983): (with an evolutionary view of disease)

A Commentary on Multiple Screening for Aminoacidopathies in the Newborn Infant.

Canadian Medical Association journal·2010

What we know that could influence future treatment of phenylketonuria.

Journal of inherited metabolic disease·2008

The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East England.

Annals of human genetics·2008

Recommendations for locus-specific databases and their curation.

Human mutation·2007

CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene.

Human mutation·2006

After the genome--the phenome?

Journal of inherited metabolic disease·2004

Diagnosis and management of childhood food allergy.

Current problems in pediatrics·2001

Spina bifida and other neural tube defects.

Current problems in pediatrics·2001

Lead poisoning: a disease for the next millennium.

Current problems in pediatrics·2000

Attention deficit-hyperactivity disorder and its deceivers.

Current problems in pediatrics·2000

Emergency medical services for children: a general pediatrician's perspective.

Current problems in pediatrics·1999

Diarrheogenic Escherichia coli.

Current problems in pediatrics·1999

Paediatric proteomic signatures of cardiometabolic disease-associated traits predict adult disease outcomes.

Nature metabolism·2026

Equitable access to cerebral palsy assessments and diagnosis through an early detection Hub: a feasibility study.

Pediatric research·2026

Paediatric Peripheral Facial Nerve Palsy-The Role of Ear Pathology.

Journal of paediatrics and child health·2026

Preschool Childhood Obesity: The Role of Parental Awareness and Nutrition Practices.

Journal of paediatrics and child health·2026

Predictive value of early treatment response for long-term outcomes after seven years on low-dose atropine.

BMJ open ophthalmology·2026

Evolving landscape of paediatric sepsis: progress, gaps and the next generation of tools.

Archives of disease in childhood·2026

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Every pediatrician a geneticist (1983): (with an evolutionary view of disease)

Related Concept Videos

A Commentary on Multiple Screening for Aminoacidopathies in the Newborn Infant.

What we know that could influence future treatment of phenylketonuria.

The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East England.

Recommendations for locus-specific databases and their curation.

CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene.

After the genome--the phenome?

Diagnosis and management of childhood food allergy.

Spina bifida and other neural tube defects.

Lead poisoning: a disease for the next millennium.

Attention deficit-hyperactivity disorder and its deceivers.

Emergency medical services for children: a general pediatrician's perspective.

Diarrheogenic Escherichia coli.

Paediatric proteomic signatures of cardiometabolic disease-associated traits predict adult disease outcomes.

Equitable access to cerebral palsy assessments and diagnosis through an early detection Hub: a feasibility study.

Paediatric Peripheral Facial Nerve Palsy-The Role of Ear Pathology.

Preschool Childhood Obesity: The Role of Parental Awareness and Nutrition Practices.

Predictive value of early treatment response for long-term outcomes after seven years on low-dose atropine.

Evolving landscape of paediatric sepsis: progress, gaps and the next generation of tools.

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Every pediatrician a geneticist (1983): (with an evolutionary view of disease)

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