OBJECTIVES: A method for training children and adults to perceive visual information without using the eyes has been developed. A study was conducted to investigate the correlation of this perceptual ...
Myotonic dystrophy 2 (DM2) is an autosomal dominant, multisystem disease, which primarily affects skeletal muscle. DM2 is caused by CCTGn expansion in the intron 1 of the ZNF9 gene. Expression of the ...
CUG triplet repeat binding protein, CUGBP1, plays a critical role in the development of skeletal muscle pathology in patients with Myotonic Dystrophy 1 (DM1). In this paper, we have characterized tran...
This brief clinical report demonstrates the necessity of supplementary examination methods for precise maxillofacial trauma diagnostics, especially in patients with combined injury. It describes the u...
The role of genetic factors in liability to schizophrenia is well established. It is supposed that different susceptibility genes produce distinct neurobiological and behavioural phenotypes that may e...