Dislexias evolutivas: qué pueden decirnos la neurología y la genética al respecto (Q58227234)

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A major susceptibility locus for specific language impairment is located on 13q21.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Different origin of auditory and phonological processing problems in children with language impairment: evidence from a twin study

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Incorporating language phenotypes strengthens evidence of linkage to autism

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Effective brain connectivity in children with reading difficulties during phonological processing

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Are specific language impairment and dyslexia distinct disorders?

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Functional roles of protein interactions with AMPA and kainate receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Evidence for a genetic aetiology in reading disability of twins.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Children's reading performance is correlated with white matter structure measured by diffusion tensor imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Tangled webs: tracing the connections between genes and cognition

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Deciphering the genetic basis of speech and language disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The genetic basis of dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Developmental dyslexia: four consecutive patients with cortical anomalies

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

From genes to behavior in developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The human lexinome: genes of language and reading

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Psychiatric endophenotypes and the development of valid animal models.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Functional genomics of neural and behavioral plasticity

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Functional connectivity of the angular gyrus in normal reading and dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Developmental dyslexia in women: neuropathological findings in three patients

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Microstructure of temporo-parietal white matter as a basis for reading ability: evidence from diffusion tensor magnetic resonance imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A transcription map of the 6p22.3 reading disability locus identifying candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Specific reading disability: differences in contrast sensitivity as a function of spatial frequency.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The relation of phoneme discrimination, lexical access, and short-term memory: A case study and interactive activation account.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD).

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Breakthroughs in the search for dyslexia candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

DCDC2 is associated with reading disability and modulates neuronal development in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Genetic influences on language impairment and phonological short-term memory.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A dominant gene for developmental dyslexia on chromosome 3

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Dyslexia: cultural diversity and biological unity

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Evidence for major gene transmission of developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The genetic basis of complex human behaviors

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Neurobiological studies of reading and reading disability

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Development of neural systems for reading

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Association of DRD4 with attention problems in normal childhood development

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Evidence That Dyslexia May Represent the Lower Tail of a Normal Distribution of Reading Ability

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Functional disruption in the organization of the brain for reading in dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Disruption of posterior brain systems for reading in children with developmental dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Neural systems for compensation and persistence: young adult outcome of childhood reading disability

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The education of dyslexic children from childhood to young adulthood

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Prevalence of speech delay in 6-year-old children and comorbidity with language impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

To see but not to read; the magnocellular theory of dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Reading disabilities: the case of Chinese, Japanese, and English

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A twin study of genetic influences on reading and spelling ability and disability.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Do different components of working memory underlie different subgroups of reading disabilities?

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Disruption of the neural response to rapid acoustic stimuli in dyslexia: evidence from functional MRI

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Neural deficits in children with dyslexia ameliorated by behavioral remediation: evidence from functional MRI.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Evidence that GRIP, a PDZ-domain protein which is expressed in the embryonic forebrain, co-activates transcription with DLX homeodomain proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

1 reference

https://api.crossref.org/works/10.1016%2FS0214-4603%2809%2970148-2

7 January 2021