Rett syndrome (RTT) is a neurodevelopmental disorder marked by profound cognitive,
communication, and motor impairments. Despite identified genotype/phenotype …

Rett syndrome (RTT) is a rare neurodevelopmental disorder primarily affecting females,
characterized by a spectrum of debilitating symptoms that impact neurological, cognitive …

Background Functional connectivity is scarcely studied in Rett syndrome (RTT). Explorations
revealed associations between RTT's clinical, genetic profiles, and coherence measures …

Background Despite being considered a rare disease, Rett syndrome is a leading cause of
profound cognitive impairment in females. This study explores game-based cognitive …

Scientific problem solving has recently attracted fixation in the field of cognitive
neuroscience and science education. Until now, there is very little evidence on the brain …

Rett syndrome (RTT) is considered a rare disease despite being the leading genetic
disorder to cause severe intellectual disability in women. There is no cure for RTT, so the …

Introduction. The degree of asymmetry in humans and the complication of mechanisms of
interhemispheric interaction are formed mainly in the process of learning. However, little …

Introduction. The ability to orientate oneself in space is one of the basic requirements for the
harmonious development of a person. The problem of human orientation in space is very …

Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked
MECP2 gene that mainly affects females and few males. The prevalence of RS is estimated …

תנייפואמה תיתוחתפתה-ורינ הערפה איה) ר” ת (טר תנומסת. םייתועמשמ םיירוטומו םייתרושקת, םייתבישח
םייוקילב הרמוחה תדימ, והוזש םייפיטונפ/םייפיטונגה םירשקה תורמל תא םיקלוחה הלא ברקב םג הלוחל …‎