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European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|November 16, 2013
Poor long-term stability of the Corvita abdominal stentgraftY Georg, N Settembre, C Marchand, et al.
The European Journal of Neuroscience|August 26, 2006
A deficiency in RFX3 causes hydrocephalus associated with abnormal differentiation of ependymal cellsD Baas, A Meiniel, C Benadiba, et al.
Blood Cells|January 1, 1994
Stem cell factor and the amplification of progenitor cells from CD34+ cord blood cellsA R Migliaccio, M Baiocchi, B Durand, et al.
Veterinary Parasitology|December 9, 2008
Animal Trichinella infection in Romania: geographical heterogeneity for the last 8 yearsR Blaga, B Durand, A Stoichici, et al.
The EMBO Journal|March 3, 1997
RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiencyB Durand, P Sperisen, P Emery, et al.
The Journal of Cardiovascular Surgery|March 22, 2012
Stent evolution for peripheral arterial diseaseA Lejay, F Thaveau, E Girsowicz, et al.
Stem Cells (Dayton, Ohio)|July 1, 1993
Aspects of the biology of the neonatal hematopoietic stem cellA R Migliaccio, M Baiocchi, B Durand, et al.
Clinical Kidney Journal|July 23, 2020
Acute peritoneal dialysis in the treatment of COVID-19-related acute kidney injuryDaniela Ponce, André L Balbi, Jonathan B Durand, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 27, 2016
Characterization of five associations of F8 missense mutations containing FVIII B domain mutationsY Jourdy, C Nougier, O Roualdes, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 25, 2015
Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiencyO Roualdes, C Nougier, M Fretigny, et al.
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