Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.
about
A Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensisA dual comparative approach: integrating lines of evidence from human evolutionary neuroanatomy and neurodevelopmental disordersBridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Verbal short-term memory deficits in Down syndrome: phonological, semantic, or both?Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.Williams syndrome-specific neuroanatomical profile and its associations with behavioral featuresPeriventricular heterotopia in common microdeletion syndromesCerebellar arachnoid cyst in a firesetter: the weight of organic lesions in arson.Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder.Developmentally altered inhibition in Ts65Dn, a mouse model of Down syndromeAn aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes.Brain imaging in neurogenetic conditions: realizing the potential of behavioral neurogenetics research.Learning by observation: insights from Williams syndromeThe cerebellum in children with spina bifida and Chiari II malformation: Quantitative volumetrics by region.Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.Down's syndrome: a genetic disorder in biobehavioral perspective.Phonological grouping is specifically affected in cerebellar patients: a verbal fluency studyTrisomy 21 and early brain developmentProfiles of everyday executive functioning in young children with down syndrome.Increased excitability and altered action potential waveform in cerebellar granule neurons of the Ts65Dn mouse model of Down syndromeDown Syndrome Developmental Brain Transcriptome Reveals Defective Oligodendrocyte Differentiation and Myelination.Dissociations in Cortical Morphometry in Youth with Down Syndrome: Evidence for Reduced Surface Area but Increased ThicknessWeaker control of the electrical properties of cerebellar granule cells by tonically active GABAA receptors in the Ts65Dn mouse model of Down's syndrome.Cerebellar vermal volumes and behavioral correlates in children with autism spectrum disorderConverging evidence for abnormalities of the prefrontal cortex and evaluation of midsagittal structures in pediatric posttraumatic stress disorder: an MRI study.MRI assessment of superior temporal gyrus in Williams syndrome.Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.Copy number variants at Williams-Beuren syndrome 7q11.23 region.Generation of improved human cerebral organoids from single copy DYRK1A knockout induced pluripotent stem cells in trisomy 21: hypothetical solutions for neurodevelopmental models and therapeutic alternatives in down syndrome.Brief report: four case histories and a literature review of Williams syndrome and autistic behavior.IV. Neuroanatomy of Williams syndrome: a high-resolution MRI study.Head circumference of children with Williams-Beuren syndrome.Fetal alcohol syndrome: a case report of neuropsychological, MRI and EEG assessment of two children.Increased glia density in the caudate nucleus in williams syndrome: Implications for frontostriatal dysfunction in autism.Abnormal development of the cerebellar vermis in children prenatally exposed to alcohol: size reduction in lobules I-V.Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structure.Isolated neurodevelopmental delay in childhood: clinicoradiological correlation in 170 patients.
P2860
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P2860
Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh-hant
name
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@en
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@nl
type
label
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@en
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@nl
prefLabel
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@en
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@nl
P1433
P1476
Anomalous brain morphology on ...... ms syndrome and Down syndrome.
@en
P2093
Jernigan TL
P304
P356
10.1001/ARCHNEUR.1990.00530050049011
P577
1990-05-01T00:00:00Z