Neural basis of an inherited speech and language disorder. - Wikidata - awgldk - TriplyDB

Neural basis of an inherited speech and language disorder.

Neural basis of an inherited speech and language disorder.

http://www.wikidata.org/entity/Q24643907

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Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder Functional and structural brain abnormalities associated with a genetic disorder of speech and language.FOXP2 is not a major susceptibility gene for autism or specific language impairment FOXP2 Human brain evolution: from gene discovery to phenotype discovery The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders The role of the basal ganglia and cerebellum in language processing Neural Correlates of Developmental Speech and Language Disorders: Evidence from Neuroimaging Human mutant huntingtin disrupts vocal learning in transgenic songbirds FOXP2 and the neuroanatomy of speech and language Voxel-based analysis of MRI reveals anterior cingulate gray-matter volume reduction in posttraumatic stress disorder due to terrorism Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders Differential FoxP2 and FoxP1 expression in a vocal learning nucleus of the developing budgerigar.Behavior-linked FoxP2 regulation enables zebra finch vocal learning Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance Left brain, right brain: facts and fantasies Shining a light on CNTNAP2: complex functions to complex disorders.Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.miR-9 and miR-140-5p target FoxP2 and are regulated as a function of the social context of singing behavior in zebra finches Expression analysis of the speech-related genes FoxP1 and FoxP2 and their relation to singing behavior in two songbird species An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning Colloquium paper: the cognitive niche: coevolution of intelligence, sociality, and language Neural representations and mechanisms for the performance of simple speech sequences.Birdsong decreases protein levels of FoxP2, a molecule required for human speech.Brain mechanisms of acoustic communication in humans and nonhuman primates: an evolutionary perspective.Abnormal functional lateralization and activity of language brain areas in typical specific language impairment (developmental dysphasia).The Role of Rhythm in Speech and Language Rehabilitation: The SEP Hypothesis Singing abilities in children with Specific Language Impairment (SLI)What developmental disorders can tell us about the nature and origins of language.Innovations in phenotyping of mouse models in the German Mouse Clinic.Early neuroimaging markers of FOXP2 intragenic deletion.Evaluation and proposal for optimization of neurophysiological tests in migraine: part 2--neuroimaging and the nitroglycerin test.Over-expression of either MECP2_e1 or MECP2_e2 in neuronally differentiated cells results in different patterns of gene expression Talking Heads Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading.Broca's area and the language instinct.A neurocognitive perspective on language: the declarative/procedural model.Monogenic and chromosomal causes of isolated speech and language impairment.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

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P2860

Neural basis of an inherited speech and language disorder.

http://www.wikidata.org/entity/Q24643907

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1998 nî lūn-bûn

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1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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1998 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年论文

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Neural basis of an inherited speech and language disorder

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Neural basis of an inherited speech and language disorder

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Neural basis of an inherited speech and language disorder

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Neural basis of an inherited speech and language disorder

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P2860

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder

Localisation of a gene implicated in a severe speech and language disorder

Feature-blind grammar and dysphagia

Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex

Prevalence of specific language impairment in kindergarten children.

Three-dimensional magnetization-prepared rapid gradient-echo imaging (3D MP RAGE).

Syndrome of acquired aphasia with convulsive disorder in children.

A new brain region for coordinating speech articulation.

Cerebral structure on magnetic resonance imaging in language- and learning-impaired children.

Noun and verb retrieval by normal subjects. Studies with PET.

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