(Q41925927)

14 October 2017

Familial epilepsy with unilateral and bilateral malformations of cortical development (English)

1 reference

14 October 2017

Bartolomei F

1

1 reference

14 October 2017

Gavaret M

series ordinal

2

1 reference

14 October 2017

Dravet C

series ordinal

3

1 reference

14 October 2017

Guerrini R

series ordinal

4

1 reference

14 October 2017

1 January 1999

1 reference

14 October 2017

1 reference

14 October 2017

40

1 reference

14 October 2017

1

1 reference

14 October 2017

47-51

1 reference

X-linked malformations of neuronal migration

14 October 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Congenital bilateral perisylvian syndrome: study of 31 patients. The CBPS Multicenter Collaborative Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Posterior agyria-pachygyria with polymicrogyria: evidence for an inherited neuronal migration disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Familial diffuse cortical dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Pachygyriclike changes: topographic appearance at MR imaging and CT and correlation with neurologic status

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Familial schizencephaly associated with EMX2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1999.TB01987.X

10.1111/J.1528-1157.1999.TB01987.X

21 January 2018

Identifiers

DOI

1 reference

14 October 2017

1 reference