The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

ανά Fremeaux-Bacchi, V, Kemp, E, Goodship, J, Dragon-Durey, M, Strain, L, Loirat, C, Deng, H, Goodship, T
Έκδοση 2005

Restricted genetic defects underlie human complement C6 deficiency

ανά DRAGON-DUREY, M A, FREMEAUX-BACCHI, V, BLOUIN, J, BARRAUD, D, FRIDMAN, W H, KAZATCHKINE, M D
Έκδοση 2003

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

ανά Fremeaux-Bacchi, V, Dragon-Durey, M, Blouin, J, Vigneau, C, Kuypers, D, Boudailliez, B, Loirat, C, Rondeau, E, Fridman, W
Έκδοση 2004

Cobalamin c deficiency associated with antifactor h antibody-associated hemolytic uremic syndrome in a young adult

ανά Philipponnet, C., Desenclos, J., Brailova, M., Aniort, J., Kemeny, J. L., Deville, C., Fremeaux-Bacchi, V., Souweine, B., Heng, A. E.
Τόπος έκδοσης BMC Nephrol (2020)

Infections Revealing Complement Deficiency in Adults: A French Nationwide Study Enrolling 41 Patients

ανά Audemard-Verger, A., Descloux, E., Ponard, D., Deroux, A., Fantin, B., Fieschi, C., John, M., Bouldouyre, A., Karkowsi, L., Moulis, G., Auvinet, H., Valla, F., Lechiche, C., Davido, B., Martinot, M., Biron, C., Lucht, F., Asseray, N., Froissart, A., Buzelé, R., Perlat, A., Boutboul, D., Fremeaux-Bacchi, V., Isnard, S., Bienvenu, B.
Τόπος έκδοσης Medicine (Baltimore) (2016)