Publications by authors named "Chartier S"

Breast magnetic resonance imaging (MRI) has the highest sensitivity for breast cancer detection compared to other breast imaging modalities such as mammography and ultrasound. As a functional modality, it captures the increased angiogenic activity of breast cancer through gadolinium-based contrast enhancement. Normal breast tissue also enhances, albeit in distinct patterns termed background parenchymal enhancement (BPE).

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Introduction: In recent years, caesarean section (CS) rate has risen worldwide. Complications associated with CS scars have risen too, such as scar dehiscences and uterine ruptures. Uterine healing is a complex phenomenon still poorly understood.

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Article Synopsis
  • * A study from a tertiary care center between 2010 and 2022 revealed a significant increase in cases (3.3-fold) during the SARS-CoV-2 pandemic compared to pre-pandemic years, though liver characteristics remained similar across both periods.
  • * Early initiation of immunosuppressive therapy was noted during the pandemic, and conducting liver biopsies is recommended for undetermined acute hepatitis cases, even if autoimmune antibodies are negative.
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The decision of when to add a new hidden unit or layer is a fundamental challenge for constructive algorithms. It becomes even more complex in the context of multiple hidden layers. Growing both network width and depth offers a robust framework for leveraging the ability to capture more information from the data and model more complex representations.

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A multilayered bidirectional associative memory neural network is proposed to account for learning nonlinear types of association. The model (denoted as the MF-BAM) is composed of two modules, the Multi-Feature extracting bidirectional associative memory (MF), which contains various unsupervised network layers, and a modified Bidirectional Associative Memory (BAM), which consists of a single supervised network layer. The MF generates successive feature patterns from the original inputs.

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Between 1983 and 2002, the incidence of solid renal tumors increased from 7.1 to 10.8 cases per 100,000.

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Cytomegalovirus (CMV) reactivation is frequent after autologous stem cell transplantation (ASCT), but generalized CMV lymphadenitis is rare. We report a CMV lymphadenitis after an ASCT mimicking a relapse of a diffuse large B-cell lymphoma. After histopathological documentation, CMV lymphadenitis should be treated to avoid systemic progression.

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Aims: High-grade metaplastic breast carcinoma (HG-MBC) is a rare subtype of invasive breast carcinoma, mostly triple-negative. Metaplastic carcinomas are less responsive to neoadjuvant chemotherapy and are associated with a worse outcome than invasive carcinomas of no special type.

Methods: Clinicopathological characteristics and immunophenotype were retrospectively assessed in a series of 65 patients diagnosed with HG-MBC between 2005 and 2017 at the Curie Institute (antibody panel: oestrogen receptor [ER], progesterone receptor [PR], androgen receptor [AR], human epidermal growth factor receptor 2 [HER2], programmed death ligand-1 [PD-L1], and trophoblast cell surface antigen 2 [TROP2]).

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Background & Aims: Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is a rare primary liver cancer (PLC) associated with a poor prognosis. Given the challenges in its identification and its clinical implications, biomarkers are critically needed. We aimed to investigate the diagnostic and prognostic value of the immunohistochemical expression of Nestin, a progenitor cell marker, in a large multicentric series of PLCs.

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Invasive fungal infections remain an important cause of complication and morbidity in the management of acute leukemias. Here we report the case of a 27-year-old patient from French Polynesia who was diagnosed with Philadelphia chromosome-negative B-cell acute lymphoblastic leukemia. After induction chemotherapy, she developed rhinosinusitis with extensive bone lysis.

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Background: Selective internal radiation therapy (SIRT) with yttrium-90 (Y) resin microspheres is an established locoregional treatment option for unresectable hepatocellular carcinoma (HCC), which delivers a lethal dose of radiation to hepatic tumors, while sparing surrounding healthy tissue. DOORwaY90 is a prospective, multicenter, open-label, single arm study, designed to evaluate the safety and effectiveness of Y resin microspheres as first-line treatment in patients with unresectable/unablatable HCC. It is unique in that it is the first study with resin microspheres to utilize a personalized Y dosimetry approach, and independent review for treatment planning and response assessment.

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Article Synopsis
  • Neuronal ceroid lipofuscinoses (NCLs) are inherited neurodegenerative disorders, primarily affecting children, caused mostly by mutations in the CTSD gene, leading to severe symptoms like microcephaly and seizures.
  • In a study of two siblings, a novel homozygous CTSD variant was identified; the first sibling experienced rapid neurological decline and died by age 24 months, while the second sibling had significant brain abnormalities observed after termination of the pregnancy.
  • This case highlights that congenital NCL related to CTSD mutations results in serious neurodegeneration and white matter atrophy, causing fast-developing microcephaly that can be fatal early in life.
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The objective of this study was to measure, via an online survey, the peritraumatic impact of COVID-19-related lockdown measures on parents and their sense of parental competence, as well as the link with their children's peritraumatic distress. We investigated the links between the distress felt by the parent and the distress felt by the child in the lockdown from March to May 2020. Participants were 287 parents and 161 children.

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Protein function is regulated by posttranslational modifications (PTMs), among which reversible oxidation of cysteine residues has emerged as a key regulatory mechanism of cellular responses. Given the redox regulation of virus-host interactions, the identification of oxidized cysteine sites in cells is essential to understand the underlying mechanisms involved. Here, we present a proteome-wide identification of reversibly oxidized cysteine sites in oxidant-treated cells using a maleimide-based bioswitch method coupled to mass spectrometry analysis.

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Sensory stimuli endow animals with the ability to generate an internal representation. This representation can be maintained for a certain duration in the absence of previously elicited inputs. The reliance on an internal representation rather than purely on the basis of external stimuli is a hallmark feature of higher-order functions such as working memory.

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Pyoderma gangrenosum is often associated with a systemic disease. Cocaine-induced pyoderma gangrenosum, most probably caused by levamisole, has been described recently and typically presents as multiple, large cribriform ulcers. Peri-nuclear antineutrophil cytoplasmic antibody is the most common serological finding.

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Cerebro-oculo-facio-skeletal syndrome (COFS) is a rare autosomal recessive neurodegenerative disease belonging to the family of DNA repair disorders, characterized by microcephaly, congenital cataracts, facial dysmorphism and arthrogryposis. Here, we describe the detailed morphological and microscopic phenotype of three fetuses from two families harboring ERCC5/XPG likely pathogenic variants, and review the five previously reported fetal cases. In addition to the classical features of COFS, the fetuses display thymus hyperplasia, splenomegaly and increased hematopoiesis.

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Purpose: The physical examination and pelvic imaging with MRI are often used in the pre-operative evaluation of pelvic organ prolapse. The objective of this study was to compare grading of prolapse on defecography phase of dynamic magnetic resonance imaging (dMRI) with physical examination (PE) grading using both the Pelvic Organ Prolapse Quantification (POP-Q) staging and Baden-Walker (BW) grading systems in the evaluation of pelvic organ prolapse (POP).

Methods: We retrospectively reviewed the charts of 170 patients who underwent dMRI at our institution.

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Recognizing and tracking the direction of moving stimuli is crucial to the control of much animal behaviour. In this study, we examine whether a bio-inspired model of synaptic plasticity implemented in a robotic agent may allow the discrimination of motion direction of real-world stimuli. Starting with a well-established model of short-term synaptic plasticity (STP), we develop a microcircuit motif of spiking neurons capable of exhibiting preferential and nonpreferential responses to changes in the direction of an orientation stimulus in motion.

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Visual motion detection is essential for the survival of many species. The phenomenon includes several spatial properties, not fully understood at the level of a neural circuit. This paper proposes a computational model of a visual motion detector that integrates direction and orientation selectivity features.

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Misfolded α-synuclein accumulates in histological inclusions constituting "Lewy pathology" found in idiopathic Parkinson disease, Parkinson disease dementia and dementia with Lewy body. The mechanism inducing α-synuclein misfolding is still unknown. The misfolded molecules form oligomers that organize into fibrils.

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Although bone is continually being remodeled and ultimately declines with aging, little is known whether similar changes occur in the sensory and sympathetic nerve fibers that innervate bone. Here, immunohistochemistry and confocal microscopy were used to examine changes in the sensory and sympathetic nerve fibers that innervate the young (10 days post-partum), adult (3 months) and aging (24 months) C57Bl/6 mouse femur. In all three ages examined, the periosteum was the most densely innervated bone compartment.

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Article Synopsis
  • The RTTN gene helps make a protein that works in tiny structures in our cells called centrosomes, and mutations in this gene are linked to brain problems in some families.
  • In one family, scientists found new mutations in the RTTN gene that were likely causing serious brain issues in their unborn babies, leading to three pregnancies being stopped.
  • The study shows that problems with the RTTN gene can cause a type of brain condition called microcephaly and also points out specific brain structure abnormalities found during research.
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