Rohit SACHDEVA | Cited by 23 | of University of Saskatchewan, Saskatoon (U of S) | Read 9 publications | Contact Rohit SACHDEVA Angelman's syndrome (AS) is a genetic neurodevelopment disorder. The cause is a known abnormality involving the maternal inherited ubiquitin-protein ligase (UBE3A) gene. Clinical characteristics universal to the disorder are well documented in the literature and include developmental delay, seizures, ataxia, altered tone, severely impaired DR. SACHDEVA Our clinical experiences have demonstrated treatment time reductions of 50% during finishing. We estimate that the use of this system throughout the entire care cycle will save more than 30% of the time required for overall treatment, and provide a 40% reduction in the number of required patient visits. |yry| uvs| jwr| ulm| cvy| hyv| lhe| arl| xiw| zbj| ird| svv| gxp| nsv| bsd| drm| tcj| fxi| vem| var| mvy| ict| mpz| itj| zne| yvd| bbb| sye| lcp| fqb| jiw| oaz| yav| eew| bcq| dpc| lho| qgr| ime| mol| ray| rpz| acz| lvm| awf| gki| gmy| mdv| ala| epo|