Variable histopathology features of neuronal dyslamination in the cerebral neocortex adjacent to epilepsy‐associated vascular malformations suggest complex pathogenesis of focal cortical dysplasia ILAE type IIIc

Dysmorphic neurons as cellular source for phase-amplitude coupling in Focal Cortical Dysplasia Type II

(2021) Stefan Rampp et al.   CLINICAL NEUROPHYSIOLOGY

Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial

(2021) Ingmar Blümcke et al.   EPILEPSIA

Seizure-mediated iron accumulation and dysregulated iron metabolism after status epilepticus and in temporal lobe epilepsy

(2021) Till S. Zimmer et al.   ACTA NEUROPATHOLOGICA

Non–Cell Autonomous Epileptogenesis in Focal Cortical Dysplasia

(2021) Hyun Yong Koh et al.   ANNALS OF NEUROLOGY

Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours

(2021) Ingmar Blumcke et al.   LANCET NEUROLOGY

Temporal analysis of histopathology and cytokine expression in the rat cerebral cortex after insulin‐induced hypoglycemia

(2020) Nagi Tomita et al.   NEUROPATHOLOGY

Somatic mutations in intracranial arteriovenous malformations

(2020) Jeremy A. Goss et al.   PLoS One

Familial Cerebral Cavernous Malformations

(2019) Atif Zafar et al.   STROKE

Arteriovenous Malformations: Congenital or Acquired Lesions?

(2019) Anastasia Tasiou et al.   World Neurosurgery

Somatic Activating KRAS Mutations in Arteriovenous Malformations of the Brain

(2018) Sergey I. Nikolaev et al.   NEW ENGLAND JOURNAL OF MEDICINE

BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumors

(2018) Hyun Yong Koh et al.   NATURE MEDICINE

High prevalence of KRAS/BRAF somatic mutations in brain and spinal cord arteriovenous malformations

(2018) Tao Hong et al.   BRAIN

A distinct clinicopathological variant of focal cortical dysplasia IIId characterized by loss of layer 4 in the occipital lobe in 12 children with remote hypoxic-ischemic injury

(2017) Dan-Dan Wang et al.   EPILEPSIA

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery

(2017) Ingmar Blumcke et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genetic and epigenetic mechanisms in the development of arteriovenous malformations in the brain

(2016) Jaya Mary Thomas et al.   Clinical Epigenetics

Characterization of radiation-induced cavernous malformations and comparison with a nonradiation cavernous malformation cohort

(2015) Jeremy K. Cutsforth-Gregory et al.   JOURNAL OF NEUROSURGERY

Sturge-Weber Syndrome Is Associated with Cortical Dysplasia ILAE Type IIIc and Excessive Hypertrophic Pyramidal Neurons in Brain Resections for Intractable Epilepsy

(2014) Dan-Dan Wang et al.   BRAIN PATHOLOGY

Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis

(2014) David A. McDonald et al.   HUMAN MOLECULAR GENETICS

Elements of morphology: General terms for congenital anomalies

(2013) Raoul C. Hennekam et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cavernoma-related epilepsy: Review and recommendations for management-Report of the Surgical Task Force of the ILAE Commission on Therapeutic Strategies

(2013) Felix Rosenow et al.   EPILEPSIA

Focal cortical dysplasia type IIIc associates with multiple cerebral cavernomas

(2013) Pitt Niehusmann et al.   EPILEPSY RESEARCH

Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ

(2013) Matthew D. Shirley et al.   NEW ENGLAND JOURNAL OF MEDICINE

Pre- and postnatal imaging of early cerebral damage in Sturge-Weber syndrome

(2013) Maud Cagneaux et al.   PEDIATRIC RADIOLOGY

Cliniconeuropathologic correlations show astroglial albumin storage as a common factor in epileptogenic vascular lesions

(2012) Anna Raabe et al.   EPILEPSIA

The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1

(2010) Ingmar Blümcke et al.   EPILEPSIA

Familial versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype

(2009) T.A. Petersen et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

An infantile-onset, severe, yet sporadic seizure pattern is common in Sturge-Weber syndrome

(2009) Eric H. Kossoff et al.   EPILEPSIA

Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy

(2009) Bruno Maton et al.   EPILEPSIA

Temporal Lobe Sclerosis Associated With Hippocampal Sclerosis in Temporal Lobe Epilepsy: Neuropathological Features

(2009) Maria Thom et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY