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The Journal of Clinical Investigation|January 21, 2025
Mycobacterium tuberculosis resisters despite HIV exhibit activated T cells and macrophages in their pulmonary alveoliMonica Dallmann-Sauer, Vinicius M Fava, Stephanus T Malherbe, et al.
BMJ Open|June 20, 2019
Multicentre, open-label, randomised, controlled clinical trial comparing 2% chlorhexidine-70% isopropanol and 5% povidone iodine-69% ethanol for skin antisepsis in reducing surgical-site infection after cardiac surgery: the CLEAN 2 study protocolMatthieu Boisson, Pierre Corbi, Thomas Kerforne, et al.
British Journal of Haematology|September 25, 2024
Impaired microvascular function in patients with sickle cell anemia and leg ulcers improved with healingJudith Catella, Etienne Turpin, Philippe Connes, et al.
Developmental Cell|May 8, 2012
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 moduleMatthew Koss, Alexandre Bolze, Andrea Brendolan, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 17, 2017
Reliability of tumor-infiltrating lymphocyte and tertiary lymphoid structure assessment in human breast cancerLaurence Buisseret, Christine Desmedt, Soizic Garaud, et al.
Bulletin Du Cancer|April 8, 2026
[Engaging professionals in quality: Understanding and adopting the FACT-JACIE accreditation process (SFGM-TC)]Gregory Elisabeth, Anne Sirvent, Agnes Perrin, et al.
Plos Genetics|November 14, 2014
A thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemiaAsmaa Mamoune, Michel Bahuau, Yamina Hamel, et al.
American Journal of Hematology|December 23, 2021
Increased blood viscosity and red blood cell aggregation in patients with COVID-19Elie Nader, Christophe Nougier, Camille Boisson, et al.
Oncoimmunology|February 16, 2017
Tumor-infiltrating lymphocyte composition, organization and PD-1/ PD-L1 expression are linked in breast cancerLaurence Buisseret, Soizic Garaud, Alexandre de Wind, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiencyCarolina Prando, Stéphanie Boisson-Dupuis, Audrey V Grant, et al.
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