Results 1 to 10 of about 41,599 (208)
Hippocampal Sclerosis: Causes and Prevention [PDF]
Hippocampal sclerosis is the commonest cause of drug-resistant epilepsy in adults, and is associated with alterations to structures and networks beyond the hippocampus.In addition to being a cause of epilepsy, the hippocampus is vulnerable to damage from seizure activity.
Matthew C Walker
exaly +3 more sources
Hippocampal Malformations Do Not Necessarily Evolve into Hippocampal Sclerosis [PDF]
Summary: Purpose:Hippocampal malformations have been proposed to underlie or evolve into hippocampal sclerosis, a common cause of refractory partial epilepsy. We report two patients with chronic epilepsy and developmental abnormalities of the hippocampus and cortex.
Arjune Sen +2 more
exaly +3 more sources
Longitudinal hippocampal atrophy in hippocampal sclerosis of aging
Hippocampal sclerosis of aging (HS-A) is a common degenerative neuropathology in older individuals and is associated with dementia. HS-A is characterized by disproportionate hippocampal atrophy at autopsy but cannot be diagnosed during life. Therefore, little is known about the onset and progression of hippocampal atrophy in individuals with HS-A.
Li, Janice X +5 more
openaire +5 more sources
Deregulation of cdk5 in Hippocampal Sclerosis [PDF]
Hippocampal sclerosis (HS) is the most common cause of chronic medically refractory epilepsy in adults. Histologically, HS is characterized by segmental neuronal loss and gliosis. Although neuronal loss is important to the pathophysiology of HS, the molecular mechanisms underlying the neuronal loss remain uncertain.
Sen, A +5 more
openaire +3 more sources
Hippocampal sclerosis dementia: a reappraisal [PDF]
Hippocampal sclerosis (HpScl) is characterized by neuronal loss and gliosis in CA1 and subiculum of the hippocampus, and may be one contributing factor to dementia in old age. The term hippocampal sclerosis dementia (HpSclD) designates the presence of both hippocampal sclerotic lesions and a dementia syndrome.
Probst A, Taylor KI, Tolnay M
openaire +3 more sources
Cardiovascular Regulation and Hippocampal Sclerosis [PDF]
Summary: Purpose:Cardiovascular dysregulation has been detected in patients with temporal lobe epilepsy (TLE) by using cardiovascular reflex tests and analysis of heart rate variability (HRV). The two methods have not previously been used in the same study to compare them in the assessment of cardioregulatory function.
Hanna, Ansakorpi +8 more
openaire +2 more sources
Corpora amylacea in hippocampal sclerosis [PDF]
Corpora amylacea have been reported in around 60% of hippocampal sclerosis specimens. The aim was to determine whether there are clinical and quantitative hippocampal MRI differences between hippocampal sclerosis with and without corpora amylacea. Corpora amylacea density was determined in 46 resected hippocampi of patients with temporal lobe epilepsy,
W, Van Paesschen, T, Revesz, J S, Duncan
openaire +2 more sources
Texture Analysis of Hippocampal Sclerosis [PDF]
Summary: Mesial temporal lobe epilepsy (MTLE) is frequently associated with refractory seizures and pathologic features of hippocampal sclerosis (HS). Quantitative magnetic resonance imaging (MRI) techniques can improve the detection and quantification of HS.
Leonardo, Bonilha +6 more
openaire +2 more sources
Cytoarchitectural Abnormalities in Hippocampal Sclerosis [PDF]
Hippocampal sclerosis (HS) is the most common pathological substrate for temporal lobe epilepsy with a characteristic pattern of loss of principle neurons primarily in CA1 and hilar subfields. Other cytoarchitectural abnormalities have been identified in human HS specimens, including dispersion of dentate granule cells and cytoskeletal abnormalities in
Maria, Thom +9 more
openaire +2 more sources
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

