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Annals of Surgery|February 18, 2010
Predicting high grade lesions of sinusoidal obstruction syndrome related to oxaliplatin-based chemotherapy for colorectal liver metastases: correlation with post-hepatectomy outcomeOlivier Soubrane, Antoine Brouquet, Stéphane Zalinski, et al.
Antimicrobial Agents and Chemotherapy|February 1, 1994
Penetration of vancomycin into mediastinal and cardiac tissues in humansC Martin, M Alaya, M N Mallet, et al.
The American Journal of Gastroenterology|November 12, 2009
Longitudinal profiles of 15 serum bile acids in patients with intrahepatic cholestasis of pregnancyRachel M Tribe, Anthony T Dann, Anna P Kenyon, et al.
Genomics|May 1, 1988
Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 lociF Xue, J R Kidd, A J Pakstis, et al.
European Journal of Gastroenterology & Hepatology|August 27, 2015
Hepatitis E infection in patients with severe alcoholic hepatitis: is there a place for systematic screening?Marika Rudler, Vincent Thibault, Sarah Mouri, et al.
Dalton Transactions (Cambridge, England : 2003)|July 2, 2016
Platinum-catalysed intermolecular addition of carbonyl compounds to 1,6-enynes: investigation of a new reaction pathwayKévin Fourmy, Mohamed El Louz, Sonia Mallet-Ladeira, et al.
Biologicals : Journal of the International Association of Biological Standardization|September 28, 2017
Validation of a PCR coupled to a microarray method for detection of mycoplasma in vaccinesEric Abachin, Marine Marius, Stéphanie Falque, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 11, 2007
[Skin to skin contact in neonatal care: knowledge and expectations of health professionals in 2 neonatal intensive care units]I Mallet, H Bomy, N Govaert, et al.
Human Molecular Genetics|October 15, 2014
Functional analysis of endoglin mutations from hereditary hemorrhagic telangiectasia type 1 patients reveals different mechanisms for endoglin loss of functionChristine Mallet, Khadija Lamribet, Sophie Giraud, et al.
Biochimica Et Biophysica Acta|December 17, 2008
Activating Fgfr3 Y367C mutation causes hearing loss and inner ear defect in a mouse model of chondrodysplasiaStéphanie Pannier, Vincent Couloigner, Nadia Messaddeq, et al.
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