Publications by authors named "S Haik"

Article Synopsis
  • Human prion diseases are unusual brain illnesses that can spread and cause quick changes in memory and thinking.
  • The study looked at a specific type called sporadic Creutzfeldt-Jakob disease (sCJD), examining data from over 3,700 cases to understand how long the disease lasts and at what age it starts.
  • Researchers found important genetic clues on chromosome 20 that can help understand how long people live with this disease, especially one specific genetic change that seems to have a big effect on survival time.
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Neuropathological diagnosis of Alzheimer disease (AD) relies on semiquantitative analysis of phosphorylated tau-positive neurofibrillary tangles (NFTs) and neuritic plaques (NPs), without consideration of lesion heterogeneity in individual cases. We developed a deep learning workflow for automated annotation and segmentation of NPs and NFTs from AT8-immunostained whole slide images (WSIs) of AD brain sections. Fifteen WSIs of frontal cortex from 4 biobanks with varying tissue quality, staining intensity, and scanning formats were analyzed.

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BackgroundPrion diseases are rare, fatal disorders that have repeatedly raised public health concerns since the early 1990s. An active prion disease surveillance network providing national level data was implemented in France in 1992.AimWe aimed to describe the epidemiology of sporadic, genetic and infectious forms of prion diseases in France since surveillance implementation.

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The development of assessment tools other than survival time is necessary to conduct therapeutic trials in prion diseases (also known as subacute transmissible encephalopathies). The Medical Research Council Prion Disease Rating Scale published by Thompson . (The Medical Research Council prion disease rating scale: A new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies.

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Article Synopsis
  • A study involving 20 COVID-19 cases identified cerebral microangiopathy in six patients, marked by changes in white matter and small artery diseases as seen on MRI.
  • The condition featured perivascular alterations such as vacuolization, macrophage clusters, and large axonal swellings, suggesting blood-brain barrier disruption without evidence of direct viral presence in the brain.
  • Detection of the SARS-CoV-2 spike protein in brain endothelial cells, particularly within the Golgi apparatus, indicates a unique interaction that might affect vascular permeability and contribute to long-term neurological effects of COVID-19.
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