Researchers at the Francis Crick Institute have pieced together genetic and molecular changes that lead to a rare progressive neurodegenerative condition called ataxia with oculomotor apraxia 2.
Jan 20, 2022
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151
A genomic architectural discovery made deep inside neurons of the brain's movement control center reveals how DNA packaging may contribute to neurodegenerative diseases. St. Jude Children's Research Hospital scientists led ...
Dec 15, 2021
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52
An international study led by Melbourne researchers has discovered nine new genes linked to the most severe type of childhood speech disorder, apraxia.
Apr 29, 2020
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An international study led by the Murdoch Children's Research Institute has made a breakthrough in identifying a potential cause of the most severe child speech impediment – apraxia.
Feb 25, 2019
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A new study indicates that children with Down syndrome who have motor speech deficits have been inadequately diagnosed, which could have a major impact on the interventions used by speech pathologists when treating patients.
Feb 4, 2016
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Some children with autism should undergo ongoing screenings for apraxia, a rare neurological speech disorder, because the two conditions often go hand-in-hand, according to Penn State College of Medicine researchers.
May 27, 2015
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Researchers from McMaster University and the Icahn School of Medicine at Mount Sinai, New York have discovered that a protein associated with neurodegenerative diseases like ALS also plays an important role in the body's ...
Mar 30, 2015
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100
Within the CogWatch European project, coordinated by the University of Birmingham, researchers at the Higher Technical School of Telecommunications Engineering and the Higher Technical School of Industrial Engineering of ...
Jul 1, 2013
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