(Q35846477)

10 August 2017

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title

The classification of cortical dysplasias through molecular genetics (English)

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10 August 2017

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Gary D Clark

1

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10 August 2017

publication date

1 September 2004

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10 August 2017

published in

Brain and Development

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10 August 2017

volume

26

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10 August 2017

issue

6

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10 August 2017

page(s)

351-362

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The place of neuronal migration abnormalities in child neurology.

10 August 2017

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The syndrome of absence of the septum pellucidum with porencephalies and other developmental defects

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Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse.

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7 January 2021

Holoprosencephaly in infants of diabetic mothers

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7 January 2021

Disorders of neuronal migration

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7 January 2021

Developmental biology. Reading the retinoid signals.

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7 January 2021

Epilepsy and anomalies of neuronal migration: MRI and clinical aspects

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7 January 2021

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

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7 January 2021

Proliferative events in the cerebral ventricular zone

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7 January 2021

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

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7 January 2021

Developmental cell death: morphological diversity and multiple mechanisms

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7 January 2021

Syndromes with cephaloceles

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7 January 2021

Retinoic acid and pattern formation in vertebrates

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7 January 2021

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7 January 2021

Detection of the reelin breakpoint in reeler mice.

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7 January 2021

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

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7 January 2021

Megalencephaly in children: Clinical syndromes, genetic patterns, and differential diagnosis from other causes of megalocephaly

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7 January 2021

Megalencephaly: types, clinical syndromes, and management

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7 January 2021

Neuropathologic findings in surgically treated hemimegalencephaly: immunohistochemical, morphometric, and ultrastructural study

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7 January 2021

Miller-Dieker syndrome: lissencephaly and monosomy 17p.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Closure of the neural tube in the cephalic region of the mouse embryo

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Genetic and neuroradiological heterogeneity of double cortex syndrome

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https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Linear nevus sebaceous syndrome: megalencephaly and heterotopic gray matter

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https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Autosomal dominant microcephaly

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https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Extreme variability of expression of a Sonic Hedgehog mutation: attention difficulties and holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Familial schizencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

The reeler gene encodes a protein with an EGF–like motif expressed by pioneer neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Magnetic resonance imaging in developmental disorders of the cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Retinoic acid embryopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Midline telencephalic dysgenesis: report of three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).

1 reference

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7 January 2021

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis

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7 January 2021

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

1 reference

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7 January 2021

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

1 reference

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7 January 2021

D-type cyclin-dependent kinase activity in mammalian cells

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7 January 2021

Identification of G1 kinase activity for cdk6, a novel cyclin D partner

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Optic nerve hypoplasia: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

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%2803%2900093-7

7 January 2021

G1 events and regulation of cell proliferation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Optic nerve hypoplasia with hypopituitarism. Septo-optic dysplasia with hypopituitarism

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

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%2803%2900093-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

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%2803%2900093-7

7 January 2021

Unusual magnetic resonance and neuropathological findings in hemimegalencephaly: report of a case following hemispherectomy.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Hemimegalencephaly: evaluation with positron emission tomography

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Letter: Hypothalamo-pituitary dysfunction in siblings of patients with holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Cell division and the nervous system: regulating the cycle from neural differentiation to death

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Do all programmed cell deaths occur via apoptosis?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Transcription factors in early development of the central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Miller-Dieker syndrome with ring chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

G1 phase progression: cycling on cue

1 reference

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7 January 2021

Neuronal migration, with special reference to developing human brain: a review

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7 January 2021

Hedgehog, the floor plate, and the zone of polarizing activity

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

An anatomic comparison of cebocephaly and ethmocephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

The tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

A Golgi study of the cerebral cortex in Fukuyama-type congenital muscular dystrophy, Walker-type "lissencephaly," and classical lissencephaly.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Isolation of 3,4-didehydroretinoic acid, a novel morphogenetic signal in the chick wing bud.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

A locus for bilateral perisylvian polymicrogyria maps to Xq28

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

Mutations in holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

22q11 deletion and polymicrogyria--cause or coincidence?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2803%2900093-7

7 January 2021

10.1016/S0387-7604(03)00093-7

Identifiers

DOI

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10 August 2017

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