The telling of the unattainable attempt to avoid the casus irreducibilis for cubic equations: Cardano's De Regula Aliza. With a compared transcription of 1570 and 1663 editions and
Joëlle Mesnil | Mon chemin vers Marc Richir 857 MoncheminversMarcRichir
L' "italianissimo", vu par Dando Dandi
Norman McLaren, artiste d’État ou les vertus créatrices de l’ascèse
« DES OREILLES IL A, TOUTEFOIS, IL N'ÉCOUTE » – ENJEUX ACOUSTIQUES DE DEUX OEUVRES CHRÉTIENNES : LES JUIFVES DE GARNIER ET LES TRAGIQUES D'AGRIPPA D'AUBIGNÉ
The Phospholipid Scramblases 1 and 4 Are Cellular Receptors for the Secretory Leukocyte Protease Inhibitor and Interact with CD4 at the Plasma Membrane
The glomerular response to IgA deposition in IgA nephropathy
Engagement of Transferrin Receptor by Polymeric IgA1: Evidence for a Positive Feedback Loop Involving Increased Receptor Expression and Mesangial Cell Proliferation in IgA Nephropathy
Association between systemic hemodynamics and septic acute kidney injury in critically ill patients: a retrospective observational study
Prognostic markers of acute decompensated heart failure: The emerging roles of cardiac biomarkers and prognostic scores
Hybrid III-V semiconductor/silicon nanolaser
Towards a monolithically integrated III–V laser on silicon: optimization of multi-quantum well growth on InP on Si
Continuous-wave operation of photonic band-edge laser at 1.55 mum on silicon wafer
Incident lacunes preferentially localize to the edge of white matter hyperintensities: insights into the pathophysiology of cerebral small vessel disease
MICA-129 genotype, soluble MICA, and anti-MICA antibodies as biomarkers of chronic graft-versus-host disease
Nomenclature for factors of the HLA system, 1995
Molecular evidence for antigen-driven immune responses in cardiac lesions of rheumatic heart disease patients
Bcl-2 protein expression is the strongest independent prognostic factor of survival in primary cutaneous large B-cell lymphomas
Demonstration of the Recurrence of Marfan-like Skeletal and Cardiovascular Manifestations Due to Germline Mosaicism for an FBN1 Mutation
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability
