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Algorithms and complexity concerning the preemptive scheduling of periodic, real-time tasks on one processor
We investigate the preemptive scheduling of periodic, real-time task systems on one processor. Expand
Pompe disease diagnosis and management guideline
Disclaimer: ACMG standards and guidelines are designed primarily as an educational resource for physicians and other health care providers to help them provide quality medical genetic services.… Expand
Strategies for Implementing Screening for Critical Congenital Heart Disease
BACKGROUND: Although newborn screening for critical congenital heart disease (CCHD) was recommended by the US Health and Human Services Secretary's Advisory Committee on Heritable Disorders in… Expand
Background: States vary widely in their use of newborn screening tests, with some mandating screening for as few as three conditions and others mandating as many as 43 conditions, including varying… Expand
Newborn Screening: Toward a Uniform Screening Panel and System—Executive Summary
The Maternal and Child Health Bureau commissioned the American College of Medical Genetics to outline a process of standardization of outcomes and guidelines for state newborn screening programs and… Expand
Phenylketonuria Scientific Review Conference: state of the science and future research needs.
New developments in the treatment and management of phenylketonuria (PKU) as well as advances in molecular testing have emerged since the National Institutes of Health 2000 PKU Consensus Statement… Expand
Pompe disease in infants and children.
Pompe disease, also referred to as glycogen storage disease type II and acid maltase deficiency, is a genetic muscle disorder caused by a deficiency of acid α-glucosidase (GAA, also referred to as… Expand
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
- Jacqueline J. Glascock, Jacinda B. Sampson, +12 authors Jill Jarecki
- Journal of neuromuscular diseases
- 26 March 2018
Background: Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by the degeneration of alpha motor neurons in the spinal cord, leading to muscular atrophy. SMA is caused by… Expand
On Asymptotic Notation with Multiple Variables
- R. Howell
We show that it is impossible to define big-O notation for functions on more than one variable in a way that implies the properties commonly used in algorithm analysis. We also demonstrate that… Expand
Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children
Abstract: The Secretary's Advisory Committee on Heritable Disorders in Newborns and Children is charged with evaluating conditions nominated for addition to the uniform screening panel and… Expand