(Q35615140)

9 August 2017

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title

Malformations of cortical development: burdens and insights from important causes of human epilepsy (English)

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9 August 2017

Sanjay M Sisodiya

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9 August 2017

publication date

1 January 2004

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9 August 2017

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9 August 2017

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9 August 2017

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9 August 2017

page(s)

29-38

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Classification system for malformations of cortical development: update 2001.

9 August 2017

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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

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Surgery for malformations of cortical development causing epilepsy

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7 January 2021

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7 January 2021

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7 January 2021

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Focal cortical dysplasia of Taylor's balloon cell type: mutational analysis of the TSC1 gene indicates a pathogenic relationship to tuberous sclerosis.

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Internexin, MAP1B, and nestin in cortical dysplasia as markers of developmental maturity

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Enhanced expression of microtubule-associated protein 2 in large neurons of cortical dysplasia

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Expression and cell distribution of group I and group II metabotropic glutamate receptor subtypes in taylor-type focal cortical dysplasia

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7 January 2021

Cajal-Retzius cells, inhibitory interneuronal populations and neuropeptide Y expression in focal cortical dysplasia and microdysgenesis

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7 January 2021

Immunocytochemical investigation on dysplastic human tissue from epileptic patients

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7 January 2021

Induced expression of NMDAR2 proteins and differential expression of NMDAR1 splice variants in dysplastic neurons of human epileptic neocortex

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7 January 2021

Decreased calmodulin-NR1 co-assembly as a mechanism for focal epilepsy in cortical dysplasia

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7 January 2021

NMDA-receptors 1 and 2A/B coassembly increased in human epileptic focal cortical dysplasia

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7 January 2021

Functional organization of the brain with malformations of cortical development

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7 January 2021

Focal cortical dysplasia: neuropathological subtypes, EEG, neuroimaging and surgical outcome

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7 January 2021

Classification issues in malformations caused by abnormalities of cortical development

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7 January 2021

Focal neuronal migration disorders and intractable partial epilepsy: results of surgical treatment

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7 January 2021

Focal transmantle dysplasia: A specific malformation of cortical development

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7 January 2021

Malformations of cortical development with balloon cells: clinical and radiologic correlates

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7 January 2021

Occipital epilepsies: identification of specific and newly recognized syndromes

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7 January 2021

Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results

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7 January 2021

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7 January 2021

Life-threatening focal status epilepticus due to occult cortical dysplasia

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7 January 2021

Surgery for catastrophic localization-related epilepsy in infants

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7 January 2021

Seizure outcome after epilepsy surgery in children and adolescents

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7 January 2021

Clinical spectrum of cortical dysplasia in childhood: diagnosis and treatment issues

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7 January 2021

Histopathological correlates of epileptogenicity as expressed by electrocorticographic spiking and seizure frequency

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7 January 2021

Prediction of surgical outcome by interictal epileptiform abnormalities during intracranial EEG monitoring in patients with extrahippocampal seizures

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7 January 2021

Surgical treatment of epilepsy due to cortical dysplasia: clinical and EEG findings

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7 January 2021

Seizure outcome after surgery for epilepsy due to malformation of cortical development

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7 January 2021

Cortical dysplasia: electroclinical, imaging, and neuropathologic study of 13 patients

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7 January 2021

Outcome of epilepsy surgery in focal cortical dysplasia

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7 January 2021

Epilepsy surgery in children with focal cortical dysplasia (FCD): results of long-term seizure outcome

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7 January 2021

Focal cortical dysplasia of Taylor's balloon cell type: a clinicopathological entity with characteristic neuroimaging and histopathological features, and favorable postsurgical outcome.

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7 January 2021

Gray matter heterotopia

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7 January 2021

Familial band heterotopias simulating tuberous sclerosis

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7 January 2021

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

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7 January 2021

Periventricular heterotopia and epilepsy.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females

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7 January 2021

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

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7 January 2021

Periventricular heterotopia associated with chromosome 5p anomalies

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7 January 2021

Autosomal recessive form of periventricular heterotopia

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7 January 2021

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation

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7 January 2021

Outcome of bilateral periventricular nodular heterotopia in monozygotic twins with megalencephaly

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7 January 2021

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7 January 2021

Multiple pterygium syndrome, bilateral periventricular nodular heterotopia and epileptic seizures--a syndrome?

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7 January 2021

Characterization of nodular neuronal heterotopia in children

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7 January 2021

Periventricular and subcortical nodular heterotopia. A study of 33 patients.

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7 January 2021

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

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7 January 2021

Seizure onset from periventricular nodular heterotopias: depth-electrode study

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7 January 2021

Stereo-EEG of interictal and ictal electrical activity of a histologically proved heterotopic gray matter associated with partial epilepsy

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7 January 2021

Function and organization in dysgenic cortex. Case report.

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7 January 2021

Bilateral parasagittal parietooccipital polymicrogyria and epilepsy

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7 January 2021

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome

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7 January 2021

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment

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7 January 2021

MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings

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7 January 2021

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

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7 January 2021

Bilateral frontal polymicrogyria and epilepsy in a patient with Turner mosaicism: a case report

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7 January 2021

A locus for bilateral perisylvian polymicrogyria maps to Xq28

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7 January 2021

Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked trait

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7 January 2021

Polymicrogyria and absence of pineal gland due to PAX6 mutation

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7 January 2021

Focal epileptogenesis in a rat model of polymicrogyria

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7 January 2021

Differential downregulation of GABAA receptor subunits in widespread brain regions in the freeze-lesion model of focal cortical malformations.

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7 January 2021

Polymicrogyria without porencephaly/schizencephaly. MRI analysis of the spectrum and the prevalence of macroscopic findings in the clinical population

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7 January 2021

Genetics of neuronal migration in the cerebral cortex

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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

Band heterotopia: Correlation of outcome with magnetic resonance imaging parameters

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7 January 2021

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

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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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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis

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7 January 2021

Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX.

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7 January 2021

Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females

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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

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7 January 2021

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome

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7 January 2021

Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations

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7 January 2021

A neuropathological, stereo-EEG, and MRI study of subcortical band heterotopia

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7 January 2021

Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate results

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7 January 2021

Dysembryoplastic neuroepithelial tumor: a surgically curable tumor of young patients with intractable partial seizures. Report of thirty-nine cases

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7 January 2021

Dysembryoplastic neuroepithelial tumor. Features in 16 patients

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7 January 2021

Radiologic appearance of the dysembryoplastic neuroepithelial tumor

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7 January 2021

Dysembryoplastic neuroepithelial tumors: nonspecific histological forms -- a study of 40 cases.

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7 January 2021

A case of dysembryoplastic neuroepithelial tumor of the parietal lobe with characteristic magnetic resonance imaging.

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7 January 2021

Dysembryoplastic neuroepithelial tumor of the cerebellum and brainstem. Case report

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7 January 2021

Dysembryoplastic neuroepithelial tumors located in the caudate nucleus area: report of four cases

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7 January 2021

Dysembryoplastic neuroepithelial tumor-like neoplasm of the septum pellucidum: a lesion often misdiagnosed as glioma: report of 10 cases

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7 January 2021

Dysembryoplastic neuroepithelial tumour of the cerebellum

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7 January 2021

Histological heterogeneity of dysembryoplastic neuroepithelial tumour: identification and differential diagnosis in a series of 74 cases

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7 January 2021

Mixed dysembryoplastic neuroepithelial tumor and ganglioglioma

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7 January 2021

Dysembryoplastic neuroepithelial tumors in two children with neurofibromatosis type 1.

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7 January 2021

Dysembryoplastic neuroepithelial tumor: radiological findings (including PET, SPECT, and MRS) and surgical strategy

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7 January 2021

Autistic spectrum disorders in childhood epilepsy surgery candidates

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7 January 2021

Malignant transformation of a dysembryoplastic neuroepithelial tumor. Case report.

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7 January 2021

Spontaneous intralesional haemorrhage in dysembryoplastic neuroepithelial tumours: a series of five cases

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7 January 2021

Dendritic development in neocortex of children with mental defect and infantile spasms

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7 January 2021

Sunrise at the synapse: the FMRP mRNP shaping the synaptic interface

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7 January 2021

Dendritic overgrowth and alterations in laminar phenotypes of neocortical neurons in the newborn with semilobar holoprosencephaly

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Microdysgenesis in surgical specimens from patients with epilepsy: occurrence and clinical correlations

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7 January 2021

Microdysgenesis in temporal lobe epilepsy. A quantitative and immunohistochemical study of white matter neurones

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7 January 2021

Temporal lobe microdysgenesis in epilepsy versus control brains

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7 January 2021

How clinicians add to knowledge of development

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7 January 2021

10.1016/S1474-4422(03)00620-3

Identifiers

DOI

1 reference

9 August 2017

1 reference