Universal screening for congenital hearing loss

Secondary biochemical and morphological consequences in lysosomal storage diseases.

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Plasma 25-hydroxyvitamin D and risk of metabolic syndrome: an ancillary analysis in the Diabetes Prevention Program.

European journal of clinical nutrition·2014

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Pediatrics·2001

Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

European journal of pediatrics·1999

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

Pediatrics·1999

Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors.

Pediatrics·1999

Centering Lived Experience: Inclusive Pediatric Care for Children Who Are Deaf and Hard of Hearing and Their Families.

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Neurodiversity and Intellectual Disability: Opportunities and Challenges for Functioning and Participation Across the Life Course.

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Action for Access: Equity for Children With Disabilities in Lowand Middle-Income Countries.

Pediatric annals·2026

Navigating Pediatric Urticaria: Diagnosis and Management for the Busy Pediatrician.

Pediatric annals·2026

A Real-World Benchmark of Monte Carlo-Assisted EKF Odometry for Online Pose Estimation in 2D LiDAR SLAM.

Sensors (Basel, Switzerland)·2026

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Healthcare (Basel, Switzerland)·2026

Multi-modal recruitment efficiency in ScreenPlus, a large-scale consented pilot NBS program.

medRxiv : the preprint server for health sciences·2026

Hybrid Code Index Modulation Based on Multi-Carrier Differential Chaos Shift Keying.

Entropy (Basel, Switzerland)·2026

Screen-Aware Reverse Tone Mapping.

Journal of imaging·2026

Frontal cortex organization supporting audiovisual processing during naturalistic viewing.

Nature communications·2026

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Universal screening for congenital hearing loss

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Secondary biochemical and morphological consequences in lysosomal storage diseases.

Plasma 25-hydroxyvitamin D and risk of metabolic syndrome: an ancillary analysis in the Diabetes Prevention Program.

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.

Glucose transporter type 1 deficiency: a study of two cases with video-EEG.

Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, Maryland.

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