(Q30635675)

25 June 2017

1 reference

title

Malformations of cortical development and epilepsy (English)

1 reference

25 June 2017

Kuzniecky RI

1

1 reference

25 June 2017

Barkovich AJ

series ordinal

2

1 reference

25 June 2017

publication date

1 March 2001

1 reference

25 June 2017

published in

Brain and Development

1 reference

25 June 2017

volume

23

1 reference

25 June 2017

issue

1

1 reference

25 June 2017

page(s)

2-11

1 reference

A classification scheme for malformations of cortical development

25 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Lissencephaly and other malformations of cortical development: 1995 update

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Microlissencephaly: a heterogeneous malformation of cortical development

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

1 reference

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Familial lissencephaly with extreme neopallial hypoplasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Hypomelanosis of Ito (incontinentia pigmenti achromians)--a clinicopathologic study: macrocephaly and gray matter heterotopias.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Hemimegalencephaly and Intractable Epilepsy: Benefits of Hemispherectomy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Focal transmantle dysplasia: a specific malformation of cortical development.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Focal dysplasia of the cerebral cortex in epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Microdysgenesis in resected temporal neocortex: Incidence and clinical significance in focal epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Cortical dysplasia in temporal lobe epilepsy: magnetic resonance imaging correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Epilepsia partialis continua due to cortical dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Temporal lobe developmental malformations and hippocampal sclerosis: epilepsy surgical outcome.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Band heterotopia: Correlation of outcome with magnetic resonance imaging parameters

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Causal heterogeneity in isolated lissencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

X-linked malformations of neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Muscle-eye-brain disease: a neuropathological study

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Fukuyama congenital muscular dystrophy: a neuroradiologic review

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Gray matter heterotopias: MR characteristics and correlation with developmental and neurologic manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Periventricular heterotopia and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Periventricular nodular heterotopia: epileptogenic findings.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Periventricular nodular heterotopia and intractable temporal lobe epilepsy: poor outcome after temporal lobe resection.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

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%2FS0387-7604%2800%2900195-9

7 January 2021

Discordant Occurrence of Cerebral Unilateral Heterotopia and Epilepsy in Monozygotic Twins

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Bilateral parasagittal parietooccipital polymicrogyria and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

A particular type of epilepsy in children with congenital hemiparesis associated with unilateral polymicrogyria.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900195-9

7 January 2021

10.1016/S0387-7604(00)00195-9

Identifiers

DOI

1 reference

release_ak2kt5ak3jgxxje6ylfvr2rdwa

25 June 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ak2kt5ak3jgxxje6ylfvr2rdwa

24 November 2022

mapped directly with Wikidata item

1 reference