Results 71 to 80 of about 713,420 (262)
Detection of Focal Cortical Dysplasia in MRI Using Textural Features
Loyek C, Woermann FG, Nattkemper TW. Detection of Focal Cortical Dysplasia in MRI Using Textural Features. In: Tolxdorff T, ed. Proceedings of BVM 2008. Informatik aktuell. Berlin, Heidelberg: Springer Verlag; 2008: 432-436.Focal cortical dysplasia (FCD)
Nattkemper, Tim Wilhelm ; https://orcid.org/ +6 more
core +1 more source
Reflex seizures and epilepsy surgery: A network approach case‐based exploration
Abstract Context Reflex seizures (RS) are defined by their consistent provocation by specific stimuli, encompassing a broad range from elementary sensory inputs to complex cognitive tasks. While RS are often encountered in clinical practice, their surgical management remains sparsely reported and poorly systematized.
Olivier Aron +6 more
wiley +1 more source
This article reviews Malformations of Cortical Development (MCD) diagnosed by Magnetic Resonance Imaging (MRI) in a series of patients with epilepsy. This study spans a five year period. The frequency of these malformations was 7.1%.
S Carvalho +8 more
doaj +1 more source
Introduction. The cessation of epileptic seizures after surgical treatment of focal epilepsy is the main objective of the surgeon. When a neurosurgeon operates focal cortical dysplasia (FCD), he/she faces difficulties with the radical removal of ...
A. A. Sufianov +8 more
doaj +1 more source
Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia
Focal cortical dysplasia (FCD) is a major cause of the sporadic form of intractable focal epilepsies that require surgical treatment. It has recently been reported that brain somatic mutations in MTOR account for 15%–25% of FCD type II (FCDII ...
임재석, 이정호, 이준학
core
Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by refractory seizures and frequently recurring epileptic activity with neurodevelopmental delay or regression that usually begin in early life. We aimed to define the relationship between electroclinical features and etiology, as well as the genotype–phenotype ...
Burcu Yaman +7 more
wiley +1 more source
KBG syndrome: A scoping review of electroclinical features of patients with epilepsy
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini +6 more
wiley +1 more source
Surgery for Cortical Malformations Causing Epilepsy
The results of surgical treatment for malformations of cortical development (MCD) causing refractory epilepsy are reviewed from the Institute of Neurology, Queen Square, London, UK.
J Gordon Millichap
doaj +1 more source
Jia Chen,1,2 Zhaoyang Huang,1,2 Liping Li,1,2 Liankun Ren,1,2 Yuping Wang1,21Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People’s Republic of China; 2Beijing Key Laboratory of ...
Ren L, Chen J, Huang Z, Wang Y, Li L
core
Anti-seizure gene therapy for focal cortical dysplasia [PDF]
Focal cortical dysplasias are a common subtype of malformation of cortical development, which frequently presents with a spectrum of cognitive and behavioural abnormalities as well as pharmacoresistant epilepsy.
Chimonides, Christos +12 more
core +1 more source

