(Q58417213)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

title

Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference

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14 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

Y Z Ekşioğlu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

P Cardenas

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

J Knoll

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

F DiMario

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

G Ramsby

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

M Berg

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

K Kamuro

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

G M Duyk

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

J Parisi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

P R Huttenlocher

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

C A Walsh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

language of work or name

English

0 references

publication date

1 January 1996

1 reference

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14 October 2019

1 reference

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14 October 2019

volume

1 reference

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14 October 2019

issue

1 reference

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14 October 2019

page(s)

77-87

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

Epileptic syndromes in childhood

14 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

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

1 reference

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7 January 2021

X-linked pachygyria and agenesis of the corpus callosum: evidence for an X chromosome lissencephaly locus

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Progress in mapping human epilepsy genes

1 reference

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7 January 2021

Familial band heterotopias simulating tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Causal heterogeneity in isolated lissencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

A linkage map of microsatellite markers on the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Identification and characterization of the tuberous sclerosis gene on chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

A 2D crossover-based map of the human X chromosome as a model for map integration

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

The GDB Human Genome Data Base anno 1994

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Identification of a second pseudoautosomal region near the Xq and Yq telomeres

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Dinucleotide repeat polymorphism in the human X-linked GABAA receptor alpha 3-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Periventricular heterotopia and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Familial periventricular nodular heterotopia

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Radial and horizontal deployment of clonally related cells in the primate neocortex: Relationship to distinct mitotic lineages

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

L1 mono- and polyclonal antibodies modify cell migration in early postnatal mouse cerebellum

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Neurons, astrocytes, and oligodendrocytes of the rat cerebral cortex originate from separate progenitor cells: an ultrastructural analysis of clonally related cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Neuropathological findings in primary generalized epilepsy: a study of eight cases

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Hereditary nodular heterotopia accompanied by mega cisterna magna

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Localization of a gene for partial epilepsy to chromosome 10q

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Separate Progenitor Cells Give Rise to Pyramidal and Nonpyramidal Neurons in the Rat Telencephalon

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Systematic widespread clonal organization in cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Partial epilepsy: chinks in the armour

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Widespread Dispersion of Neuronal Clones Across Functional Regions of the Cerebral Cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Integration of gene maps: chromosome X

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

A second generation linkage map of the human genome based on highly informative microsatellite loci

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980025-2

7 January 2021

10.1016/S0896-6273(00)80025-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8562093%20AND%20SRC:MED&resulttype=core&format=json