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

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

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http://www.wikidata.org/entity/Q57949908
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalitiesMeCP2 controls BDNF expression and cocaine intake through homeostatic interactions with microRNA-212.Perspectives on hand function in girls and women with Rett syndrome.Variations of stereotypies in individuals with Rett syndrome: A nationwide cross-sectional study in Taiwan.The Incidence and Evolution of Parkinsonian Rigidity in Rett Syndrome: A Pilot Study.The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.Developmental Profile and Diagnoses in Children Presenting with Motor Stereotypies.Clinical approach to motor stereotypies in autistic children.Trihexyphenidyl for acute life-threatening episodes due to a dystonic movement disorder in Rett syndrome.Stereotypical hand movements in 144 subjects with Rett syndrome from the population-based Australian database.MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome.Using a large international sample to investigate epilepsy in Rett syndrome.Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome.Comparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life.Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective.Loss of Causes Atypical Synaptic and Molecular Plasticity of Parvalbumin-Expressing Interneurons Reflecting Rett Syndrome-Like Sensorimotor Defects
P2860

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

Item
http://www.wikidata.org/entity/Q57949908
description
article
@en
im Juli 2008 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в липні 2008
@uk
name
Movement disorders in Rett syn ...... correlation with mutation type
@en
Movement disorders in Rett syn ...... correlation with mutation type
@nl
type
label
Movement disorders in Rett syn ...... correlation with mutation type
@en
Movement disorders in Rett syn ...... correlation with mutation type
@nl
prefLabel
Movement disorders in Rett syn ...... correlation with mutation type
@en
Movement disorders in Rett syn ...... correlation with mutation type
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Movement disorders in Rett syn ...... correlation with mutation type
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698