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Review reveals evidence behind alternative immobilization methods for pediatric patients

As a parent, you want to protect your child from getting hurt; however, avoiding bumps, bruises and broken bones isn't always possible.

9 Jan 2020

Parental enforcement of bedtime yields solid results for sleep-deprived teens

Teenagers in the US simply don't get enough shut eye. The consequences of this epidemic of sleep deprivation are extensive and include increasing rates of anxiety and depression among adolescents, as well as suicidal thoughts and actions.

9 Jan 2020

One-fourth of children with autism miss diagnosis, study finds

One-fourth of children under age 8 with autism spectrum disorder - most of them black or Hispanic - are not being diagnosed, which is critical for improving quality of life.

9 Jan 2020

Missing a key protein in the brain can cause autism-like behaviors

Scientists at Rutgers University-Newark have discovered that when a key protein needed to generate new brain cells during prenatal and early childhood development is missing, part of the brain goes haywire - causing an imbalance in its circuitry that can lead to long-term cognitive and movement behaviors characteristic of autism spectrum disorder.

9 Jan 2020

UMSOM research shows even milder cases of diarrheal diseases can lead to child mortality

Diarrheal diseases are a leading cause of death for young children, accounting for nine percent of all deaths worldwide in children under five years of age, with most occurring in children under two years of age.

9 Jan 2020

First-ever genomic analysis of puberty yields insights into critical areas of human health

In the first-ever genome-scale analysis of the puberty process in humans, researchers at Huntsman Cancer Institute at the University of Utah outline distinct and critical changes to stem cells in males during adolescence.

9 Jan 2020

Scientists identify 'modifier gene' that determines severity of inherited kidney disease

Scientists have developed a new way to understand complex genetic diseases and have identified a gene that modifies the severity of inherited kidney disease, paving the way for personalised treatments.

9 Jan 2020

Addressing resilience, emotional health within families of children with chronic conditions

Be it autism, sickle cell or other life-disrupting health conditions, being the parent of a child with a chronic condition takes a psychological toll. For too many families, however, emotional and behavioral health support has been far too difficult to obtain.

9 Jan 2020

New AI system determines aggressiveness of prostate cancer better than most pathologists

Researchers at Radboud university medical center have developed a 'deep learning' system that is better than most pathologists at determining the aggressiveness of prostate cancer. The AI system, which uses tissue samples to arrive at its diagnosis, taught itself to identify prostate cancer based on data from over 1200 patients.

9 Jan 2020

Judo holds promise for reducing sedentary behavior among children with autism

Judo may be just the right sport to increase the physical activity level among children with autism spectrum disorder and holds promise for reducing sedentary behavior, which is linked to obesity and diabetes, according to a new study from the University of Central Florida.

9 Jan 2020

Kangaroo mother care increases survival of low birth weight babies

Researchers at Centre for Intervention Science in Maternal and Child Health at the University of Bergen followed 8400 low birth weight infants, from 2015 to 2018.

9 Jan 2020

Poor early life environment leaves permanent mark on adult brain

A severely deprived child may never really recover from the impact of deprivation early in life, finds a new study.

9 Jan 2020

Timing is key: preventing infant SHIV infection by PEP

Researchers tested methods to prevent development of SHIV, an infection similar to HIV, in infant macaque monkeys.

9 Jan 2020

Maternal microbiota is a source of newborn immunity, shows study

Mother's milk has been long touted for its salutary effects on the newborn and its ability to shield infants from certain infections.

9 Jan 2020

Findings may lead to potential therapeutic strategies for rare neurodevelopmental disorder

The brain undergoes dramatic change during the first years of life. Its circuits readily rewire as an infant and then child encounters new sights and sounds, taking in the world and learning to understand it.

9 Jan 2020

Study: Environment changes can impact stability landscape of the gut microbial community

Your fingerprints stay the same all your life. But what about the "fingerprint" of microbial strains that are shared in the guts of childhood twins?

9 Jan 2020

Post-mortem genetic testing used to find underlying cause of sudden deaths in Amish families

Researchers used post-mortem genetic testing to find the underlying cause of multiple sudden deaths in young people and sudden cardiac arrests in two large Amish families.

8 Jan 2020

Researchers use single cell genome sequencing to study malaria transmission

New technology employing single cell genome sequencing of the parasite that causes malaria has yielded some surprising results and helps pave the way for possible new intervention strategies for this deadly infectious disease, according to Texas Biomedical Research Institute Assistant Professor Ian Cheeseman, Ph.D. Dr. Cheeseman was Principal Investigator of a three-year study published in the January 2020 edition of Cell Host & Microbe, a high-impact peer-reviewed publication.

8 Jan 2020

Minimally invasive technique to directly measure cardiac output in newborns

The amount of blood that the heart pumps in one minute (cardiac output) can be directly measured safely in newborns by monitoring changes in blood velocity after injecting saline, indicates a paper published online Dec. 17, 2019 in the Journal of Pediatrics and Neonatal Medicine.

8 Jan 2020

Cystic fibrosis carriers have higher risk for all CF-related conditions

Conventional wisdom says that having just one mutated copy of the cystic fibrosis gene has no effects on a person's health--the disease occurs when both copies of the gene are mutated. But a new study from the University of Iowa suggests that may not be the case.

8 Jan 2020

Children News and Research

Review reveals evidence behind alternative immobilization methods for pediatric patients

Parental enforcement of bedtime yields solid results for sleep-deprived teens

One-fourth of children with autism miss diagnosis, study finds

Missing a key protein in the brain can cause autism-like behaviors

UMSOM research shows even milder cases of diarrheal diseases can lead to child mortality

First-ever genomic analysis of puberty yields insights into critical areas of human health

Scientists identify 'modifier gene' that determines severity of inherited kidney disease

Addressing resilience, emotional health within families of children with chronic conditions

New AI system determines aggressiveness of prostate cancer better than most pathologists

Judo holds promise for reducing sedentary behavior among children with autism

Kangaroo mother care increases survival of low birth weight babies

Poor early life environment leaves permanent mark on adult brain

Timing is key: preventing infant SHIV infection by PEP

Maternal microbiota is a source of newborn immunity, shows study

Findings may lead to potential therapeutic strategies for rare neurodevelopmental disorder

Study: Environment changes can impact stability landscape of the gut microbial community

Post-mortem genetic testing used to find underlying cause of sudden deaths in Amish families

Researchers use single cell genome sequencing to study malaria transmission

Minimally invasive technique to directly measure cardiac output in newborns

Cystic fibrosis carriers have higher risk for all CF-related conditions

Industry Focus eBook - Neurology/Neuroscience - 2nd edition eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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