Longitudinal MRI brain findings in the R1349Q pathogenic variant of CACNA1A
Pathogenic CACNA1A gene variants are associated with a spectrum of disorders including migraine with or without hemiplegia, ataxia, epilepsy, and developmental disability.
Chang Y. Ho, MD +3 more
doaj +1 more source
The prevalence of seizures and epilepsy and the occurrence of other brain malformations or structural abnormalities were examined in 81 children with meningomyelocele followed at the multidisciplinary Children’s Clinics for Rehabilitative Services ...
J Gordon Millichap
doaj +1 more source
Memory Performance is Related to Language Dominance as Determined by the intracarotid amobarbital procedure [PDF]
Objective The goal of this study was to explore the relationship between language and memory lateralization in patients with epilepsy undergoing the intracarotid amobarbital procedure.
Alexopoulosa, A. V. +7 more
core +2 more sources
Afasia e herpes vírus: estudo de caso [PDF]
CONTEXT: Meningoencephalitis early in life, of any etiology, is a risk factor for development of subsequent sequelae, which may be of physical, psychiatric, behavioral or cognitive origin.
Cera, Maysa Luchesi +3 more
core +1 more source
Factor XIII deficiency in a neonate presenting as subpial haemorrhage
Subpial haemorrhage is a rare cause of seizures in term neonates. A 3-day-old male infant, born at term with no history of perinatal hypoxia, presented with seizures and unremarkable physical examination in the interictal state. Imaging demonstrated left
Monish G. Karthikeyan +2 more
doaj +1 more source
Exploration of gray matter correlates of cognitive training benefit in adolescents with chronic traumatic brain injury [PDF]
Sustaining a traumatic brain injury (FBI) during adolescence has a profound effect on brain development and can result in persistent executive functioning deficits in daily life.
Caeyenberghs, Karen +5 more
core +2 more sources
Large midline persistent parietal foramina with occipital encephalocele and abnormal venous drainage
Enlarged persistent parietal foramen is rare congenital skull defect and associated anomalies like underlying encephalomalacia, and venous malformations are known.
Parag Agarwal +3 more
doaj +1 more source
Complex pattern of interaction between in utero hypoxia-ischemia and intra-amniotic inflammation disrupts brain development and motor function [PDF]
Background: Infants born preterm commonly suffer from a combination of hypoxia-ischemia (HI) and infectious perinatal inflammatory insults that lead to cerebral palsy, cognitive delay, behavioral issues and epilepsy.
Berglass, Jacqueline +6 more
core +1 more source
Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina +11 more
wiley +1 more source
Pancreatic Encephalopathy- A Rare Complication of Severe Acute Biliary Pancreatitis [PDF]
Background. Pancreatic encephalopathy is a rare complication of severe acute pancreatitis, with high mortality, being difficult to diagnose and treat, thus requiring continuous research regarding its management. Materials and Methods.
Bobic, Simona +3 more
core +2 more sources

