(Q34216765)

31 July 2017

1 reference

title

Cell migration and cerebral cortical development (English)

1 reference

31 July 2017

1 reference

Golden JA

1

1 reference

PubMed ID

11298998

31 July 2017

language of work or name

1 reference

1 February 2001

1 reference

Neuropathology and Applied Neurobiology

31 July 2017

1 reference

31 July 2017

27

1 reference

31 July 2017

22-28

1 reference

31 July 2017

1

1 reference

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

31 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Diagnostic criteria for Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Lissencephaly and other malformations of cortical development: 1995 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.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/10.1046%2FJ.0305-1846.2001.00307.X

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Lissencephaly-pachygyria associated with congenital cytomegalovirus infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Norman-Roberts syndrome: clinical and molecular studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Lissencephaly associated with congenital hypomyelinating and axonal neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.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/10.1046%2FJ.0305-1846.2001.00307.X

Development of the cortical dysplasia of type II lissencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

Genetic malformations of the human cerebral cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0305-1846.2001.00307.X

10.1046/J.0305-1846.2001.00307.X

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference

PubMed ID

11298998