The hyperkinetic movement disorder ofFOXG1-related epileptic-dyskinetic encephalopathy

Forkhead Box G1 Gene Haploinsufficiency: An Emerging Cause of Dyskinetic Encephalopathy of Infancy

(2015) Matteo Cassina et al.   NEUROPEDIATRICS

Epilepsy and outcome inFOXG1-related disorders

(2014) Laurie E. Seltzer et al.   EPILEPSIA

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

(2013) Peter D. Stenson et al.   HUMAN GENETICS

Epilepsy in Rett syndrome, andCDKL5- andFOXG1-gene-related encephalopathies

(2012) Renzo Guerrini et al.   EPILEPSIA

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

(2011) F. Kortum et al.   JOURNAL OF MEDICAL GENETICS

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation

(2011) Aurélie Méneret et al.   MOVEMENT DISORDERS

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

(2010) L. Deprez et al.   NEUROLOGY

A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorder

(2009) MICHAEL ABSOUD et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

(2008) Francesca Ariani et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Combination of infantile spasms, non-epileptic seizures and complex movement disorder: A new case of ARX-related epilepsy

(2008) Karine Poirier et al.   EPILEPSY RESEARCH

Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

(2008) Teresa Temudo et al.   MOVEMENT DISORDERS