Neurology News

‘MARRVEL’ new way to compile big data in human-centric wayMay 11, 2017
A group of researchers at Baylor created MARRVEL to help researchers everywhere search databases all at once and in a matter of minutes.
‘Silent seizures’ found in patients with Alzheimer’s diseaseMay 1, 2017
Discovery of ‘Silent seizures’ provides a better understanding of Alzheimer’s disease and can potentially lead to new treatments.
Zoghbi honored with Canada International Gairdner Award Mar 28, 2017
Dr. Huda Zoghbi is being honored by the Gairdner Foundation with the 2017 Canada Gairdner International Award for seminal discoveries and contributions to biomedical science.
Mouse study helps find causes of human behavioral disordersMar 13, 2017
Research of a mouse model led to the discovery of the genetic cause of the human neurological condition of five patients who, until now, had not received a genetic diagnosis.
Algorithm gives insight into auditory/visual illusionFeb 16, 2017
Neuroscience researchers have created an algorithm to reveal key insight into why the brain can sometimes muddle up one of the most fundamental aspects of the human experience.
Vital links between brain tumors, epileptic seizures foundFeb 7, 2017
Research suggests detecting brain tumors at the earliest possible stage and eliminating them before seizures begin might be possible one day.
Monthly Evenings with Genetics seminar to focus on Parkinson’s in JanuaryJan 18, 2017
The next installment of Evenings with Genetics will focus on Parkinson’s disease, with expert speakers providing an overview of treatment for the disease, along with future directions in care.
Bipolar disorder and epilepsy linked to turning down an inhibitory switch in brain circuits Jan 3, 2017
Researchers have shown a link between epilepsy and how a gene associated with bipolar disorder controls the balance between brain excitation and inhibition.
Genes Nardilysin and OGDHL linked to human neurological conditionsDec 22, 2016
An international team of scientists has discovered that the gene, OGDHL, a key protein required for normal function of the mitochondria and its chaperone, nardilysin are linked to progressive loss of neurological function in humans.
Genetic cause identified for previously unrecognized developmental disorderDec 22, 2016
Baylor scientists are part of an international team that has identified variants of the gene EBF3, which causes a developmental disorder with features in common with autism.