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Rett’s Syndrome and full inclusionSíndrome de Rett e inclusão
(Universidade Federal de Santa Maria, 2008)
Síndrome de Rett: estudo retrospectivo e prospectivo de 28 pacientesRett syndrome: retrospective and prospective study of 28 patients
(Academia Brasileira de Neurologia - ABNEURO, 2001)
Un caso de síndrome de RettA case of Rett syndrome
(SABER ULA, 2005)
Un caso de síndrome de RettA case of Rett syndrome
(SABER ULA, 2005)
The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome
(W.B. Saunders Ltd, 2019)
Rett syndrome (RTT) is an early-onset neurodevelopmental disorder that is caused by mutations in the MECP2 gene; however, defects in other genes (CDKL5 and FOXG1) can lead to presentations that resemble classic RTT, although ...
Quantification of functional abilities in Rett syndrome: a comparison between stages III and IV
(Dove Medical Press Ltd, 2014-01-01)
We aimed to evaluate the functional abilities of persons with Rett syndrome (RTT) in stages III and IV. The group consisted of 60 females who had been diagnosed with RTT: 38 in stage III, mean age (years) of 9.14, with a ...