8 results match your criteria: "University and Hospital of Poitiers[Affiliation]"

Purpose: Monitoring and predicting the cognitive state of subjects with neurodegenerative disorders is crucial to provide appropriate treatment as soon as possible. In this work, we present a machine learning approach using multimodal data (brain MRI and clinical) from two early medical visits, to predict the longer-term cognitive decline of patients. Using transfer learning, our model can be successfully transferred from one neurodegenerative disease (Alzheimer's) to another (Parkinson's).

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Attention-guided neural network for early dementia detection using MRS data.

Comput Med Imaging Graph

July 2022

DACTIM-MIS, LMA, URM CNRS 7348, University of Poitiers, France; I3M, Common Laboratory CNRS-Siemens-Healthineers, University and Hospital of Poitiers, France.

Imaging bio-markers have been widely used for Computer-Aided Diagnosis (CAD) of Alzheimer's Disease (AD) with Deep Learning (DL). However, the structural brain atrophy is not detectable at an early stage of the disease (namely for Mild Cognitive Impairment (MCI) and Mild Alzheimer's Disease (MAD)). Indeed, potential biological bio-markers have been proved their ability to early detect brain abnormalities related to AD before brain structural damage and clinical manifestation.

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A Hybrid Method for 3D Reconstruction of MR Images.

J Imaging

April 2022

Common Laboratory Multi-Nuclear Multi-Organ Metabolic Imaging (I3M), CNRS-Siemens, University and Hospital of Poitiers, 86000 Poitiers, France.

Three-dimensional surface reconstruction is a well-known task in medical imaging. In procedures for intervention or radiation treatment planning, the generated models should be accurate and reflect the natural appearance. Traditional methods for this task, such as Marching Cubes, use smoothing post processing to reduce staircase artifacts from mesh generation and exhibit the natural look.

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Glioma is one of the most important central nervous system tumors, ranked 15th in the most common cancer for men and women. Magnetic Resonance Imaging (MRI) represents a common tool for medical experts to the diagnosis of glioma. A set of multi-sequences from an MRI is selected according to the severity of the pathology.

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The automatic segmentation of multiple sclerosis lesions in magnetic resonance imaging has the potential to reduce radiologists' efforts on a daily time-consuming task and to bring more reproducibility. Almost all new segmentation techniques make use of convolutional neural networks with their own different architecture. Architectural choices are rarely explained.

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Article Synopsis
  • Familial Mediterranean fever (FMF) is a genetic autoinflammatory disorder linked to an imbalance between the cytokine IL-1β and its antagonist IL-1RA.
  • A study genotyped 42 FMF patients and 42 controls to investigate genetic polymorphisms in IL-1β and IL-1RA genes, finding associations with disease occurrence and severity.
  • Results showed that specific IL-1β gene polymorphisms (CC genotype at -31 and +3954) were more common in FMF patients and correlated with increased IL-1β secretion and higher disease severity.
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In order to clarify the inflammatory mechanism underlying familial Mediterranean fever (FMF), we aimed to evaluate the ex vivo cytokine profile of FMF patients during acute attacks and attack-free periods, and compare it with that of healthy controls. The study included 34 FMF patients, of whom 9 were studied during attack and remission and 24 healthy controls. Cytokine levels were evaluated by Luminex technology in serum and supernatants of PBMC (Peripheral Blood Mononuclear Cells) cultures with and without 24h stimulation of monocytes by LPS and T lymphocytes by anti-CD3/CD28 beads.

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Article Synopsis
  • - The Atlas of Genetics and Cytogenetics in Oncology and Haematology is a peer-reviewed online resource that focuses on genes related to cancer and hereditary diseases, offering a wealth of information, including review articles and extensive iconography.
  • - It integrates various types of data such as genetic abnormalities, histopathology, and clinical diagnoses, evolving from traditional methods to advanced techniques like massive sequencing for more comprehensive insights.
  • - This resource serves as a valuable tool for researchers and clinicians, aiding in cytogenetic diagnosis and informing treatment decisions, especially for rare diseases.
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