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The American Journal of Pathology|August 30, 2005
Overexpression of insulin receptor substrate-2 in human and murine hepatocellular carcinomaMathieu Boissan, Eléonore Beurel, Dominique Wendum, et al.
AJR. American Journal of Roentgenology|April 18, 2002
Feasibility and effectiveness of using coronary stents in the treatment of hepatic artery stenoses after orthotopic liver transplantation: preliminary reportAlban L Denys, Salah D Qanadli, François Durand, et al.
Canadian Medical Association Journal|November 1, 1983
Acute graft-versus-host disease after allogeneic bone marrow transplantationC Perreault, M Gyger, J Boileau, et al.
HIV Medicine|September 30, 2025
Impact on weight of a Doravirine switch in people living with HIVNina Garofoli, Philippe Flandre, Jean-Paul Vincensini, et al.
Orphanet Journal of Rare Diseases|November 13, 2025
Pain assessment and treatment in patients with mucopolysaccharidoses: a French multicentric pediatric studyMélanie Blin, Marine Tardieu, Didier Lacombe, et al.
Journal of Bioscience and Bioengineering|August 14, 2017
Optimized transitory ectopic expression of promastigote surface antigen protein in Nicotiana benthamiana, a potential anti-leishmaniasis vaccine candidateSéverine Lacombe, Martine Bangratz, Jean-Paul Brizard, et al.
Journal of the Neurological Sciences|November 8, 2017
Orthostatic hypotension associated with executive dysfunction in mild cognitive impairmentChristian Bocti, François Pépin, Maxime Tétreault, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|September 5, 2017
Development of anti-hepatitis B surface (HBs) antibodies after HBs antigen loss in HIV-hepatitis B virus co-infected patientsAnders Boyd, Laetitia Canini, Joël Gozlan, et al.
Elife|December 7, 2020
The half-life of the bone-derived hormone osteocalcin is regulated through <i>O</i>-glycosylation in mice, but not in humansOmar Al Rifai, Catherine Julien, Julie Lacombe, et al.
Clinical Genetics|November 22, 2022
Aminoacylation-defective bi-allelic mutations in human EPRS1 associated with psychomotor developmental delay, epilepsy, and deafnessDanni Jin, Sheree A Wek, Ricardo A Cordova, et al.
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