(Q42478885)

English

X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".

scientific article published on April 2005

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scholarly article

1 reference

Europe PubMed Central

1 November 2017

X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy". (English)

1 reference

Europe PubMed Central

1 November 2017

0 references

X-linked lissencephaly with abnormal genitalia

1 reference

based on heuristic

inferred from title

intractable epilepsy

1 reference

based on heuristic

inferred from title

William B. Dobyns

2

object named as

William B Dobyns

1 reference

Europe PubMed Central

1 November 2017

author name string

Mitsuhiro Kato

1

1 reference

Europe PubMed Central

1 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 April 2005

1 reference

Europe PubMed Central

1 November 2017

Journal of Child Neurology

1 reference

Europe PubMed Central

1 November 2017

20

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Europe PubMed Central

1 November 2017

4

1 reference

Europe PubMed Central

1 November 2017

392-397

1 reference

Europe PubMed Central

1 November 2017

Modes of neuronal migration in the developing cerebral cortex

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Mode of cell migration to the superficial layers of fetal monkey neocortex

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Lissencephaly and the molecular basis of neuronal migration

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

A four-layered 'lissencephalic' cortex induced by prenatal X-irradiation in the rat.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Opposing actions of Arx and Pax4 in endocrine pancreas development

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

The biology of epilepsy genes

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Inherited disorders of ion transport in the intestine

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Diffuse pachygyria with cerebellar hypoplasia: a milder form of microlissencephaly or a new genetic syndrome?

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Characterization and classification of neonatal seizures.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Neonatal seizures: diagnosis and treatment

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Prediction of outcome based on clinical seizure type in newborn infants.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Neonatal seizures: early-onset seizure syndromes and their consequences for development

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

A case of early myoclonic encephalopathy with the congenital nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

A long, remarkable journey: tangential migration in the telencephalon.

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

New concepts in neonatal seizures

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200042001

21 January 2018

Identifiers

10.1177/08830738050200042001

1 reference

Europe PubMed Central

1 November 2017

1 reference

Europe PubMed Central

1 November 2017

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