Manifeste contre les attaques infligées aux droits des autochtones du Brésil

Mai 2017 Nous, professeurs, intellectuels et universitaires, manifestons avec véhémence notre refus de la politique anti-autochtone de l’État brésilien et notre préoccupation vis-à-vis d’une politique qui a déjà des conséquences génocidaires dans les États du Mato Grosso do Sul, de Bahia et du Maranhão. Ces cinq dernières années, les attaques contre les droits autochtones se sont aggravées et ont permis leur révision en autorisant la contestation légale des droits acquis. Les droits constitut..

Magnetically Guided Laser Surgery for the Treatment of Twin-to-Twin Transfusion Syndrome

Twin-to-twin transfusion syndrome (TTTS) is a severe disorder that often leads to the death of monochorionic twin fetuses, if left untreated. Current prenatal interventions to treat the condition involve the use of rigid fetoscopes for targeted laser coagulation of the vascular anastomoses. These tools are limited in their area of operation, making treatment challenging, especially in cases with anterior placentation. Herein, a robotic platform to perform this task using remote magnetic navigation is proposed. In contrast to rigid tools, the presented custom magnetic fetoscope is highly flexible, dexterous, and has considerable advantages, including safety and precision. A visual servoing algorithm that allows the surgeon to navigate in the uterus with submillimeter precision is introduced. The system has been validated on ex vivo human placentas in a setting that mimics the real intraoperative conditions

SND@LHC: The Scattering and Neutrino Detector at the LHC

SND@LHC is a compact and stand-alone experiment designed to perform measurements with neutrinos produced at the LHC in the pseudo-rapidity region of ${7.2 < \eta < 8.4}$. The experiment is located 480 m downstream of the ATLAS interaction point, in the TI18 tunnel. The detector is composed of a hybrid system based on an 830 kg target made of tungsten plates, interleaved with emulsion and electronic trackers, also acting as an electromagnetic calorimeter, and followed by a hadronic calorimeter and a muon identification system. The detector is able to distinguish interactions of all three neutrino flavours, which allows probing the physics of heavy flavour production at the LHC in the very forward region. This region is of particular interest for future circular colliders and for very high energy astrophysical neutrino experiments. The detector is also able to search for the scattering of Feebly Interacting Particles. In its first phase, the detector will operate throughout LHC Run 3 and collect a total of 250 $\text{fb}^{-1}$

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

The known breast cancer (BC) susceptibility polymorphisms in FGFR2, TNRC9/TOX3, MAP3K1,LSP1 and 2q35 confer increased risks of BC for BRCA1 or BRCA2 mutation carriers. We evaluated the associations of three additional SNPs, rs4973768 in SLC4A7/NEK10, rs6504950 in STXBP4/COX11 and rs10941679 at 5p12 and reanalyzed the previous associations using additional carriers in a sample of 12,525 BRCA1 and 7,409 BRCA2 carriers. Additionally, we investigated potential interactions between SNPs and assessed the implications for risk prediction. The minor alleles of rs4973768 and rs10941679 were associated with increased BC risk for BRCA2 carriers (per-allele Hazard Ratio (HR)=1.10, 95%CI:1.03-1.18, p=0.006 and HR=1.09, 95%CI:1.01-1.19, p=0.03, respectively). Neither SNP was associated with BC risk for BRCA1 carriers and rs6504950 was not associated with BC for either BRCA1 or BRCA2 carriers. Of the nine polymorphisms investigated, seven were associated with BC for BRCA2 carriers (FGFR2, TOX3, MAP3K1, LSP1, 2q35, SLC4A7, 5p12, p-values:7×10−11-0.03), but only TOX3 and 2q35 were associated with the risk for BRCA1 carriers (p=0.0049, 0.03 respectively). All risk associated polymorphisms appear to interact multiplicatively on BC risk for mutation carriers. Based on the joint genotype distribution of the seven risk associated SNPs in BRCA2 mutation carriers, the 5% of BRCA2 carriers at highest risk (i.e. between 95th and 100th percentiles) were predicted to have a probability between 80% and 96% of developing BC by age 80, compared with 42-50% for the 5% of carriers at lowest risk. Our findings indicated that these risk differences may be sufficient to influence the clinical management of mutation carriers

Jurisprudence du Tribunal Administratif de l'Organisation Internationale du Travail

Dreyfus Simone. Jurisprudence du Tribunal Administratif de l'Organisation Internationale du Travail. In: Annuaire français de droit international, volume 4, 1958. pp. 332-340

H. Clastres, La Terre sans Mal. Le prophétisme tupi-guarani

Dreyfus Simone. H. Clastres, La Terre sans Mal. Le prophétisme tupi-guarani. In: L'Homme, 1976, tome 16 n°2-3. pp. 167-169

David Maybury-Lewis, The Savage and the innocent

Dreyfus Simone. David Maybury-Lewis, The Savage and the innocent. In: L'Homme, 1966, tome 6 n°4. pp. 108-109

R. Cardoso de Oliveira, O Processo de Assimilação dos Terêna

Dreyfus Simone. R. Cardoso de Oliveira, O Processo de Assimilação dos Terêna. In: L'Homme, 1961, tome 1 n°3. pp. 126-129

1.2. Les Sateré-Mawé et les Mundurucu : l'affaire Elf-Aquitaine

Dreyfus-Gamelon Simone. 1.2. Les Sateré-Mawé et les Mundurucu : l'affaire Elf-Aquitaine . In: Journal de la Société des Américanistes. Tome 70, 1984. pp. 181-185