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Search Results

Showing results 21 to 40 of 304.

Article

Evaluation of x-linked adrenoleukodystrophy newborn screening in North Carolina

January 31, 2020
Article

North Carolina newborn exome sequencing for universal screening (NC nexus) detects molecular etiologies underlying inborn errors of metabolism and hearing loss

November 01, 2019
Article

Supporting informed clinical trial decisions: Results from a randomized controlled trial evaluating a digital decision support tool for those with intellectual disability

October 23, 2019
Article

The North Carolina experience with mucopolysaccharidosis type I newborn screening

August 01, 2019
Article

Early check: Translational science at the intersection of public health and newborn screening

July 17, 2019
Article

Early check: Studying the benefits of early detection and intervention

July 01, 2019
Article

The future of newborn screening: Why and how partnerships will be needed for success

January 10, 2019
Article

Early check: A North Carolina research partnership

January 10, 2019
Article

Early identification of fragile X syndrome through expanded newborn screening

January 03, 2019
Article

A digital health app to assess decisional capacity to provide informed consent: Protocol for a randomized controlled trial

November 19, 2018
Article

Developmental trajectories of executive functions in young males with fragile X syndrome

October 01, 2018
Article

Skills attained by infants with congenital Zika syndrome: Pilot data from Brazil

July 26, 2018
Article

A comparison of functional academic and daily living skills in males with fragile X syndrome with and without autism

July 01, 2018
Article

Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: A randomized controlled trial protocol

June 28, 2018
Article

A digital decision support tool to enhance decisional capacity for clinical trial consent: Design and development

June 06, 2018
Article

Early check: A voluntary newborn screening program and research registry to facilitate clinical trials in pre-symptomatic infants with rare diseases

May 01, 2018
Article

Values clarification exercises improved parental decision making about newborn genomic sequencing

April 01, 2018
Article

Decision making in couples offered genomic sequencing for newborn screening: Outcomes of a surrogate, joint decision

April 01, 2018
Article

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: A discrete-choice experiment

February 01, 2018
Article

The likely impact of congenital zika syndrome on families: Considerations for family supports and services

February 01, 2018