Magnetic resonance imaging: role in the understanding of cerebral malformations (Q30667222)

26 June 2017

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title

Magnetic resonance imaging: role in the understanding of cerebral malformations (English)

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26 June 2017

A James Barkovich

1

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26 June 2017

1 January 2002

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26 June 2017

Brain and Development

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26 June 2017

24

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26 June 2017

1

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26 June 2017

2-12

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The molecular biology of axon guidance

26 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Development of the corpus callosum and cavum septi in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Holoprosencephaly: a paradigm for the complex genetics of brain development.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Focal transmantle dysplasia: a specific malformation of cortical development.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Microlissencephaly: a heterogeneous malformation of cortical development

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

7 January 2021

Frontal and central lobe focal dysplasia: clinical, EEG and imaging features.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

A classification scheme for malformations of cortical development

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Cerebrospinal fluid cleft with cortical dimple: MR imaging marker for focal cortical dysgenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Focal cortical dysplasia: comparison of MRI and FDG-PET.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

EEG, PET, SPET and MRI in intractable childhood epilepsies: possible surgical correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Improved sensitivity of 18FDG-positron emission tomography scans in frontal and "frontal plus" epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

1 reference

7 January 2021

Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Causal heterogeneity in isolated lissencephaly

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2FS0387-7604%2801%2900327-8

7 January 2021

Band heterotopia: Correlation of outcome with magnetic resonance imaging parameters

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Genetic and neuroradiological heterogeneity of double cortex syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

7 January 2021

The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

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%2801%2900327-8

7 January 2021

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Pneumographic demonstration of subependymal heterotopic cortical gray matter in children.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Callosal agenesis with cyst: a better understanding and new classification

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Gray matter heterotopia

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Periventricular heterotopia and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

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%2801%2900327-8

7 January 2021

Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

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%2801%2900327-8

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%2801%2900327-8

7 January 2021

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

The small GTPase RalA targets filamin to induce filopodia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

A tension-based theory of morphogenesis and compact wiring in the central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

A genetic animal model of human neocortical heterotopia associated with seizures

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Heterotopic neurogenesis in a rat with cortical heterotopia.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Early vascularization of the embryonic cerebral cortex: Golgi and electron microscopic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

1 reference

7 January 2021

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Bilateral parasagittal parietooccipital polymicrogyria and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Bilateral perisylvian polymicrogyria in three generations.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Bilateral central macrogyria: epilepsy, pseudobulbar palsy, and mental retardation--a recognizable neuronal migration disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Microgyria in the distribution of the middle cerebral artery in a patient with DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Bilateral opercular polymicrogyria

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Towards a greater understanding of the pathogenesis of holoprosencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Macroscopic susceptibility in ultra high field MRI. II: acquisition of spin echo images from the human head

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

High resolution MRI of the brainstem at 8 T.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Phased array detectors and an automated intensity-correction algorithm for high-resolution MR imaging of the human brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: application to white matter fiber tract mapping in the human brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Visualizing and characterizing white matter fiber structure and architecture in the human pyramidal tract using diffusion tensor MRI.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

In vivo fiber tractography using DT-MRI data

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

Fiber crossing in human brain depicted with diffusion tensor MR imaging.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900327-8

7 January 2021

10.1016/S0387-7604(01)00327-8

Identifiers

DOI

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26 June 2017

1 reference

PubMed ID

11751019