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Study identifies mutations in single genes that can be responsible for cerebral palsy

The causes of cerebral palsy have long been debated and often are attributed to in utero infections, premature birth, or brain injury to the baby near or during delivery, usually from a lack of oxygen. But many young children diagnosed with cerebral palsy have not experienced such events.

30 Sep 2020

New tool can employ MRI scan data to predict motor development risks for preterm infants

As many as 70% of very premature infants (born earlier than 32 weeks gestation) show signs of white matter abnormalities at birth. But only some of those infants go on to develop cognitive, language, motor, or behavioral disorders as they grow.

30 Sep 2020

Persistent-poverty counties face high risk of cancer mortality

Residents of counties that experience persistent poverty face a disproportionately high risk of cancer mortality, according to a study published in Cancer Epidemiology, Biomarkers & Prevention, a journal of the American Association for Cancer Research.

30 Sep 2020

Cancer chemotherapy changes the function of cells that repair heart injury

Cancer chemotherapy changes the function of cells that repair heart injury, researchers at The University of Texas Health Science Center at San Antonio (UT Health San Antonio) discovered.

30 Sep 2020

Oral antibiotics are effective for treating cystic fibrosis, shows new clinical trial

A major national study led by experts from Bristol and Nottingham has found that oral antibiotics are just as effective as intravenous antibiotics in killing a common germ that causes dangerous complications in cystic fibrosis (CF) patients.

30 Sep 2020

Different triggers for Kawasaki disease suggest slightly different genetic susceptibilities

Researchers at University of California San Diego report that while Kawasaki disease (KD) occurs in clusters, the traits, and thus the triggers of the inflammatory disease vary among clusters. The findings are published in the September 2020 online issue of The Journal of Pediatrics.

30 Sep 2020

Scientists identify mutations in single genes linked to certain cases of cerebral palsy

30 Sep 2020

Acid reflux drug could help newborns recover from hypoxic-ischemic encephalopathy

Researchers in China have discovered a potential way to prevent a lack of oxygen or blood flow from causing long-lasting brain damage in newborn children.

29 Sep 2020

Increased hydroxyproline levels may be associated with joint hypermobility in autistic children

A team of researchers found out that children with autistic spectrum disorder (ASD) have increased levels of the amino acid hydroxyproline.

29 Sep 2020

Australian scientists develop a nasal spray that could stop SARS-CoV-2 infection

The novel product, called INNA-051, is being developed by Ena Respiratory, and laboratory experiments have shown that it reduced viral replication by as much as 96 percent in the animal study. Spearheaded by Public Health England’s (PHE) Deputy Director, Professor Miles Carroll, the new study described the potential treatment and has been published in the open-source preprint server bioRxiv*.

29 Sep 2020

Nasal calcium-rich salts effectively eliminate airborne particles from airways

In a paper published in Molecular Frontiers Journal, researchers from Cambridge, Massachusetts have discovered a more effective way of eliminating airborne particles from airways using nasal calcium-rich salts called FEND, which have potential applications in the fight against Covid-19.

29 Sep 2020

Computer model unravels mystery behind severe inflammation in people with COVID-19

A study from the University of Pittsburgh School of Medicine and Cedars-Sinai addresses a mystery first raised in March: Why do some people with COVID-19 develop severe inflammation?

29 Sep 2020

Girls participating in sports show improved behavior, attentiveness in early adolescence

Girls - but not boys - who participate actively in school sports activities in middle childhood show improved behavior and attentiveness in early adolescence, suggests a new Canadian study published in Preventative Medicine.

29 Sep 2020

Cincinnati Children's research leads to approval of new drug for hypereosinophilic syndrome

Following two decades of research on a group of rare diseases called hypereosinophilic syndrome at Cincinnati Children's Hospital Medical Center, the U.S. Food and Drug Administration has approved the drug Nucala (mepolizumab) for use in the treatment of patients with hypereosinophilic syndrome.

28 Sep 2020

Healthy vitamin D levels could reduce COVID-19 complications

Published in the journal PLOS ONE, the study investigates the link between serum 25-hydroxyvitamin D levels and its effect on adverse clinical outcomes and parameters of immune function and mortality due to COVID-19.

28 Sep 2020

New study reveals the impacts of COVID-19 on unborn children

What are the risks to an unborn child if a woman contracts COVID-19 while pregnant, and how can doctors identify which pregnancies are at greater risk of adverse outcomes if a pregnant mother tests positive?

28 Sep 2020

One-third of parents in the U.S. won’t get flu shots for their kids during the pandemic

A survey from the National Poll on Children’s Health, however, revealed that one-third of American parents have no plans of getting their children vaccinated for the flu virus this year during the COVID-19 pandemic.

28 Sep 2020

Stanford researchers unravel how a common genetic deletion elevates schizophrenia risk

A common genetic deletion boosts the risk for schizophrenia by 30-fold. Generating nerve cells from people with the deletion has showed Stanford researchers why.

28 Sep 2020

Researchers discover specific cellular pathway involved in lung tissue regeneration

Researchers at Children's Hospital of Philadelphia and the Perelman School of Medicine at the University of Pennsylvania have identified a cellular pathway that can be targeted with a naturally occurring drug to stimulate lung tissue regeneration, which is necessary for recovery from multiple lung injuries.

28 Sep 2020

Brain wiring genes may be linked to a significant portion of cerebral palsy cases

In an article published in Nature Genetics, researchers confirm that about 14% of all cases of cerebral palsy, a disabling brain disorder for which there are no cures, may be linked to a patient's genes and suggest that many of those genes control how brain circuits become wired during early development.

28 Sep 2020

Children News and Research

Study identifies mutations in single genes that can be responsible for cerebral palsy

New tool can employ MRI scan data to predict motor development risks for preterm infants

Persistent-poverty counties face high risk of cancer mortality

Cancer chemotherapy changes the function of cells that repair heart injury

Oral antibiotics are effective for treating cystic fibrosis, shows new clinical trial

Different triggers for Kawasaki disease suggest slightly different genetic susceptibilities

Scientists identify mutations in single genes linked to certain cases of cerebral palsy

Acid reflux drug could help newborns recover from hypoxic-ischemic encephalopathy

Increased hydroxyproline levels may be associated with joint hypermobility in autistic children

Australian scientists develop a nasal spray that could stop SARS-CoV-2 infection

Nasal calcium-rich salts effectively eliminate airborne particles from airways

Computer model unravels mystery behind severe inflammation in people with COVID-19

Girls participating in sports show improved behavior, attentiveness in early adolescence

Cincinnati Children's research leads to approval of new drug for hypereosinophilic syndrome

Healthy vitamin D levels could reduce COVID-19 complications

New study reveals the impacts of COVID-19 on unborn children

One-third of parents in the U.S. won’t get flu shots for their kids during the pandemic

Stanford researchers unravel how a common genetic deletion elevates schizophrenia risk

Researchers discover specific cellular pathway involved in lung tissue regeneration

Brain wiring genes may be linked to a significant portion of cerebral palsy cases

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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