Results 101 to 110 of about 55,381 (288)
Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley +1 more source
Frontiers in Neuroscience, 2019 Diabetes affects the morphology and plasticity of the hippocampus, and leads to learning and memory deficits. Caffeine has been proposed to prevent memory impairment upon multiple chronic disorders with neurological involvement.
João M. N. Duarte +12 more
doaj +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain +6 more
wiley +1 more source
ID02 Post Papilledema Gliosis [PDF]
Post papilledema milky gliosis with arteriolar constriction and atrophy, 1982, left eye, pair with ID_1. Anatomy: Optic disc. Pathology: Post papilledema atrophy and gliosis due to huge anterior communicating artery aneurysm. Disease/ Diagnosis: Elevated
William F. Hoyt, MD
core
Frontiers in Neuroscience, 2018 Intracerebral hemorrhage (ICH) is a fatal stroke subtype with significant public health impact. Although neuroinflammation is a leading cause of neurological deficits after ICH, no imaging tool is currently available to monitor brain inflammation in ICH ...
Frederick Bonsack +5 more
doaj +1 more source
Annals of Neurology, EarlyView.Objective Drug‐resistant epilepsy (DRE) remains a clinical challenge, as therapies modifying disease trajectory are lacking. Increasing evidence implicates gut microbiota dysbiosis in epilepsy pathophysiology, with short‐chain fatty acids (SCFAs) emerging as key microbial metabolites with neuroprotective and anti‐inflammatory properties.
Akash A. Bera +16 more
wiley +1 more source
ID01 Post Papilledema Gliosis [PDF]
Post papilledema milky gliosis with arteriolar constriction, 1982, right eye, pair with ID_2. Anatomy: Optic disc. Pathology: Post papilledema atrophy and gliosis due to huge anterior communicating artery aneurysm.
William F. Hoyt, MD
core
Reactive gliosis in the injured brain: The effect of cell communication and Nrf2-mediated cellular defence [PDF]
, 2011 Stroke and other brain injuries trigger an extensive glial cell response referred to as reactive gliosis. Reactive gliosis is characterized by hypertrophic and proliferating astrocytes, proliferating microglia and NG2-positive cells, which eventually ...
Andersson, Heléne, Bergström, Petra
core +1 more source
Annals of the Child Neurology Society, EarlyView.ABSTRACT Objective Seizures represent a significant source of morbidity for children with brain tumors. The objective of our study was to establish consensus guidelines for managing children with tumor‐related epilepsy. Methods The study team assembled a panel of 18 child neurologists specializing in neurological complications of brain tumors including
Stephanie N. Brosius +4 more
wiley +1 more source
Massive retinal gliosis: An unusual case with immunohistochemical study [PDF]
, 2011 Massive retinal gliosis (MRG) is a rare, benign intraocular condition that results from the proliferation of well-differentiated glial cells. Immunohistochemically, these cells show positivity for glial fibrillary acid protein (GFAP), neuron specific ...
Amrut V Ashturkar +9 more
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