Propranolol, a drug that is efficacious against infantile haemangiomas ("strawberry naevi," resembling birthmarks), can also be used to treat cerebral cavernous malformations, a condition characterized by misshapen blood ...
Feb 23, 2021
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Research carried out by scientists at the Centro Nacional de Investigaciones Cardiovasculares (CNIC) advances the understanding of the biology of blood vessels, and points the way to the design of new therapeutic strategies ...
Dec 9, 2020
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A study led by researchers at the Centenary Institute has identified a drug currently used to treat cancer patients, as a potential treatment option for a leading cause of stroke in young people.
Nov 7, 2018
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About 1 in 750 babies born in the United States has some kind of craniofacial malformation, accounting for about one-third of all birth defects.
Jan 25, 2018
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Bacteria in the gut microbiome drive the formation of cerebral cavernous malformations (CCMs), clusters of dilated, thin-walled blood vessels in the brain that can cause stroke and seizures, according to new research published ...
May 10, 2017
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Cerebral cavernous malformations (CCMs) are clusters of dilated, thin-walled blood vessels in the brain that can cause stroke and seizures, yet exactly how they form is somewhat of a mystery. Now, a team from the Perelman ...
Mar 30, 2016
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(Medical Xpress)—Researchers have pinpointed the role of a gene known as Arl13b in guiding the formation and proper placement of neurons in the early stages of brain development. Mutations in the gene could help explain ...
Jul 2, 2013
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(Medical Xpress)—A new gene associated with a form of congenital heart disease in newborn babies – known as "a hole in the heart" has been discovered by researchers.
May 27, 2013
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Maternal use of valproate (a drug used for the treatment of epilepsy and other neuropsychological disorders) during pregnancy was associated with a significantly increased risk of autism in offspring, according to a study ...
Apr 23, 2013
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Researchers at the University of California, San Francisco and in Michigan, North Carolina and Spain have discovered how genetic mutations cause a number of rare human diseases, which include Meckel syndrome, Joubert syndrome ...
Jul 8, 2011
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