List of works - Eric E Smeets

Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study.

scientific article published on 2 January 2018

Communication in Individuals with Rett Syndrome: an Assessment of Forms and Functions.

scientific article

De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

scientific article

Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability

scientific article published on 07 December 2018

Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands

scientific article published on 19 October 2015

Incontinence in Individuals with Rett Syndrome: A Comparative Study ⬇️

scientific article published on February 23, 2012

Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes

article

Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes

scientific article published on 25 March 2019

MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients

scientific article

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

scientific journal article

Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. ⬇️

scientific article

New insights in Rett syndrome using pathway analysis for transcriptomics data

scientific article

Oculomotor Function in Individuals With Rett Syndrome

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

scientific article published on 2 November 2017

Rett Syndrome as a Rare Disease: A European Perspective

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes

scientific article (publication date: 25 November 2016)

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes

Rett syndrome and developmental regression

scientific article published on 05 July 2019

Rett syndrome: A study of the face ⬇️

scientific article published on May 27, 2011

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.

scientific article

List of works by Eric E Smeets

Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study.

Communication in Individuals with Rett Syndrome: an Assessment of Forms and Functions.

De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability

Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands

Incontinence in Individuals with Rett Syndrome: A Comparative Study ⬇️

Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes

Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes

MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. ⬇️

New insights in Rett syndrome using pathway analysis for transcriptomics data

Oculomotor Function in Individuals With Rett Syndrome

Oculomotor Function in Individuals With Rett Syndrome

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

Rett Syndrome as a Rare Disease: A European Perspective

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes

Rett syndrome and developmental regression

Rett syndrome: A study of the face ⬇️

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.