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Synaptic hyperexcitability of cytomegalic pyramidal neurons contributes to epileptogenesis in tuberous sclerosis complex

Cell reports (Cambridge), 2022-07, Vol.40 (3), p.111085-111085, Article 111085

2022

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A Mouse Model of Tuberous Sclerosis: Neuronal Loss of Tsc1 Causes Dysplastic and Ectopic Neurons, Reduced Myelination, Seizure Activity, and Limited Survival

The Journal of neuroscience, 2007-05, Vol.27 (21), p.5546-5558

2007

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Co-expression of NMDA-receptor subunits NR1, NR2A, and NR2B in dysplastic neurons of teratomas in patients with paraneoplastic NMDA-receptor-encephalitis: a retrospective clinico-pathology study of 159 patients

Acta neuropathologica communications, 2020-08, Vol.8 (1), p.1-15, Article 130

2020

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Brain overgrowth in disorders of RTK–PI3K–AKT signaling: A mosaic of malformations

Seminars in perinatology, 2015-02, Vol.39 (1), p.36-43

Hevner, Robert F., MD, PhD

2015

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Aberrant neuronal-glial differentiation in Taylor-type focal cortical dysplasia (type IIA/B)

Acta neuropathologica, 2005-05, Vol.109 (5), p.519-533

2005

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Cellular localization of metabotropic glutamate receptors in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex

Neuroscience, 2008-09, Vol.156 (1), p.203-215

2008

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Abundance of LRP12 C-rs9694676 allelic promoter variant in epilepsy-associated gangliogliomas

Life sciences (1973), 2016-06, Vol.155, p.70-75

2016

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Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex

Neuropathology, 2008-12, Vol.28 (6), p.577-590

2008

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Cellular distribution of vascular endothelial growth factor A (VEGFA) and B (VEGFB) and VEGF receptors 1 and 2 in focal cortical dysplasia type IIB

Acta neuropathologica, 2008-06, Vol.115 (6), p.683-696

2008

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Doublecortin‐like (DCL) expression in focal cortical dysplasia and cortical tubers

Epilepsia (Copenhagen), 2009-12, Vol.50 (12), p.2629-2637

2009

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Intractable epilepsy: Expression of substance P in cortical dysplastic neurons

Pediatrics international, 2009-06, Vol.51 (3), p.418-421

2009

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Expression and cellular distribution of high- and low-affinity neurotrophin receptors in malformations of cortical development

Acta neuropathologica, 2004-11, Vol.108 (5), p.422-434

2004

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Intractable epilepsy: Expression of substance P in cortical dysplastic neurons

Pediatrics International, 2009, Vol.51 (3), p.418-421

2009

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COGNITIVE DYSFUNCTION AND OTHER COMORBIDITIES | The Relationship of Epilepsy to Other Conditions/Disorders

Encyclopedia of Basic Epilepsy Research, p.181-185

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Capsaicin: Friend or Foe in Skin Cancer and Other Related Malignancies?

Nutrients, 2017-12, Vol.9 (12), p.1365

2017

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Array analysis of epilepsy-associated gangliogliomas reveals expression patterns related to aberrant development of neuronal precursors

Brain (London, England : 1878), 2008-11, Vol.131 (11), p.3034-3050

2008

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Infection with JC Virus and Possible Dysplastic Ganglion-Like Transformation of the Cerebral Cortical Neurons in a Case of Progressive Multifocal Leukoencephalopathy

Journal of neuropathology and experimental neurology, 2000-10, Vol.59 (10), p.921-929

2000

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Vascular contrast enhancement in Lhermitte-Duclos disease : case report

Neuroradiology, 1995-10, Vol.37 (7), p.545-548

1995

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Dysplastic glioneuronal lesion arising in the cerebellum: a clinicopathological, immunohistochemical and ultrastructural study

Clinical neuropathology, 2001-03, Vol.20 (2), p.73

2001

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Linear nevus sebaceous syndrome: Megalencephaly and heterotopic gray matter

Pediatric neurology, 1991, Vol.7 (1), p.45-49

1991

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Recurrent dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) presenting with subarachnoid haemorrhage

British journal of neurosurgery, 1992, Vol.6 (2), p.153-156

1992

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Lhermitte-Duclos disease

Acta neuropathologica, 1983-01, Vol.59 (2), p.88-94

1983

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Synaptic hyperexcitability of cytomegalic pyramidal neurons contributes to epileptogenesis in tuberous sclerosis complex

A Mouse Model of Tuberous Sclerosis: Neuronal Loss of Tsc1 Causes Dysplastic and Ectopic Neurons, Reduced Myelination, Seizure Activity, and Limited Survival

Co-expression of NMDA-receptor subunits NR1, NR2A, and NR2B in dysplastic neurons of teratomas in patients with paraneoplastic NMDA-receptor-encephalitis: a retrospective clinico-pathology study of 159 patients

Brain overgrowth in disorders of RTK–PI3K–AKT signaling: A mosaic of malformations

Aberrant neuronal-glial differentiation in Taylor-type focal cortical dysplasia (type IIA/B)

Cellular localization of metabotropic glutamate receptors in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex

Abundance of LRP12 C-rs9694676 allelic promoter variant in epilepsy-associated gangliogliomas

Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex

Cellular distribution of vascular endothelial growth factor A (VEGFA) and B (VEGFB) and VEGF receptors 1 and 2 in focal cortical dysplasia type IIB

Doublecortin‐like (DCL) expression in focal cortical dysplasia and cortical tubers

Intractable epilepsy: Expression of substance P in cortical dysplastic neurons

Expression and cellular distribution of high- and low-affinity neurotrophin receptors in malformations of cortical development

Intractable epilepsy: Expression of substance P in cortical dysplastic neurons

COGNITIVE DYSFUNCTION AND OTHER COMORBIDITIES | The Relationship of Epilepsy to Other Conditions/Disorders

Capsaicin: Friend or Foe in Skin Cancer and Other Related Malignancies?

Array analysis of epilepsy-associated gangliogliomas reveals expression patterns related to aberrant development of neuronal precursors

Infection with JC Virus and Possible Dysplastic Ganglion-Like Transformation of the Cerebral Cortical Neurons in a Case of Progressive Multifocal Leukoencephalopathy

Vascular contrast enhancement in Lhermitte-Duclos disease : case report

Dysplastic glioneuronal lesion arising in the cerebellum: a clinicopathological, immunohistochemical and ultrastructural study

Linear nevus sebaceous syndrome: Megalencephaly and heterotopic gray matter

Recurrent dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease) presenting with subarachnoid haemorrhage

Lhermitte-Duclos disease

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