Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills
about
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsA new look at an old drug: neuroprotective effects and therapeutic potentials of lithium saltsUsing Sibling Designs to Understand Neurodevelopmental Disorders: From Genes and Environments to Prevention ProgrammingPhelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoringPhelan-McDermid Syndrome and SHANK3: Implications for Treatment.The spectrum of epilepsy and electroencephalographic abnormalities due to SHANK3 loss-of-function mutationsA pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndromeDNA methylation profiling in the thalamus and hippocampus of postnatal malnourished mice, including effects related to long-term potentiation.Lithium as a rescue therapy for regression and catatonia features in two SHANK3 patients with autism spectrum disorder: case reports.Case report: an unexpected link between partial deletion of the SHANK3 gene and Heller's dementia infantilis, a rare subtype of autism spectrum disorder.Post-transcriptional regulation of SHANK3 expression by microRNAs related to multiple neuropsychiatric disordersDevelopmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children.Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.Modeling autism by SHANK gene mutations in mice.Phelan McDermid Syndrome: From Genetic Discoveries to Animal Models and Treatment.SHANK Mutations May Disorder Brain Development.Loss of skills and onset patterns in neurodevelopmental disorders: Understanding the neurobiological mechanisms.Identification of 22q13 genes most likely to contribute to Phelan McDermid syndrome.Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers.Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome).nArgBP2-SAPAP-SHANK, the core postsynaptic triad associated with psychiatric disorders.Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
P2860
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P2860
Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills
description
2012 nî lūn-bûn
@nan
2012 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@ast
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@en
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@nl
type
label
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@ast
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@en
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@nl
prefLabel
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@ast
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@en
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@nl
P2093
P2860
P3181
P356
P1476
Neuropsychopathology in 7 Pati ...... and Progressive Loss of Skills
@en
P2093
G Van Buggenhout
H Van Esch
J Geutjens
J-P Frijns
K Devriendt
T de Ravel
P2860
P3181
P356
10.1159/000339119
P407
P577
2012-06-01T00:00:00Z