Terminal Complement Inhibitor Eculizumab in Atypical Hemolytic–Uremic Syndrome
Legendre, C.M, Licht, C, Muus, P, Greenbaum, L.A, Babu, S, Bedrosian, C, Bingham, C, Cohen, D.J, Delmas, Y, Douglas, K, Eitner, F, Feldkamp, T, Fouque, D, Furman, R.R, Gaber, O, Herthelius, M, Hourmant, M, Karpman, D, Lebranchu, Y, Mariat, C, Menne, J, Moulin, B, Nürnberger, J, Ogawa, M, Remuzzi, G, Richard, T, Sberro-Soussan, R, Severino, B, Sheerin, N.S, Trivelli, A, Zimmerhackl, L.B, Goodship, T, Loirat, C
Published in The New England journal of medicine (06.06.2013)
Published in The New England journal of medicine (06.06.2013)
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Complement Genes Strongly Predict Recurrence and Graft Outcome in Adult Renal Transplant Recipients with Atypical Hemolytic and Uremic Syndrome
Le Quintrec, M., Zuber, J., Moulin, B., Kamar, N., Jablonski, M., Lionet, A., Chatelet, V., Mousson, C., Mourad, G., Bridoux, F., Cassuto, E., Loirat, C., Rondeau, E., Delahousse, M., Frémeaux‐Bacchi, V.
Published in American journal of transplantation (01.03.2013)
Published in American journal of transplantation (01.03.2013)
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Journal Article
Eculizumab for Atypical Hemolytic Uremic Syndrome Recurrence in Renal Transplantation
Zuber, J., Le Quintrec, M., Krid, S., Bertoye, C., Gueutin, V., Lahoche, A., Heyne, N., Ardissino, G., Chatelet, V., Noël, L.‐H., Hourmant, M., Niaudet, P., Frémeaux‐Bacchi, V., Rondeau, E., Legendre, C., Loirat, C.
Published in American journal of transplantation (01.12.2012)
Published in American journal of transplantation (01.12.2012)
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Population pharmacokinetics and pharmacogenetics of tacrolimus in de novo pediatric kidney transplant recipients
Zhao, W, Elie, V, Roussey, G, Brochard, K, Niaudet, P, Leroy, V, Loirat, C, Cochat, P, Cloarec, S, André, J L, Garaix, F, Bensman, A, Fakhoury, M, Jacqz-Aigrain, E
Published in Clinical pharmacology and therapeutics (01.12.2009)
Published in Clinical pharmacology and therapeutics (01.12.2009)
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A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
Besbas, N., Karpman, D., Landau, D., Loirat, C., Proesmans, W., Remuzzi, G., Rizzoni, G., Taylor, C.M., Van de Kar, N., Zimmerhackl, L.B.
Published in Kidney international (01.08.2006)
Published in Kidney international (01.08.2006)
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A Randomized Trial to Assess the Impact of Early Steroid Withdrawal on Growth in Pediatric Renal Transplantation: The TWIST Study
Grenda, R., Watson, A., Trompeter, R., Tönshoff, B., Jaray, J., Fitzpatrick, M., Murer, L., Vondrak, K., Maxwell, H., Van Damme‐Lombaerts, R., Loirat, C., Mor, E., Cochat, P., Milford, D. V., Brown, M., Webb, N. J. A.
Published in American journal of transplantation (01.04.2010)
Published in American journal of transplantation (01.04.2010)
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The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
Dragon-Durey, M-A, Blanc, C, Marliot, F, Loirat, C, Blouin, J, Sautes-Fridman, C, Fridman, W H, Frémeaux-Bacchi, V
Published in Journal of medical genetics (01.07.2009)
Published in Journal of medical genetics (01.07.2009)
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Journal Article
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome
Fremeaux-Bacchi, V, Dragon-Durey, M-A, Blouin, J, Vigneau, C, Kuypers, D, Boudailliez, B, Loirat, C, Rondeau, E, Fridman, W H
Published in Journal of medical genetics (01.06.2004)
Published in Journal of medical genetics (01.06.2004)
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Initial presentation of childhood-onset systemic lupus erythematosus: A French multicenter study
Bader-Meunier, B., Armengaud, J.B., Haddad, E., Salomon, R., Deschênes, G., Koné-Paut, I., Leblanc, T., Loirat, C., Niaudet, P., Piette, J.C., Prieur, A.M., Quartier, P., Bouissou, F., Foulard, M., Leverger, G., Lemelle, I., Pilet, P., Rodière, M., Sirvent, N., Cochat, P., the French pediatric-onset SLE study group
Published in The Journal of pediatrics (01.05.2005)
Published in The Journal of pediatrics (01.05.2005)
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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
Gbadegesin, Rasheed, Hinkes, Bernward G., Hoskins, Bethan E., Vlangos, Christopher N., Heeringa, Saskia F., Liu, Jinhong, Loirat, Chantal, Ozaltin, Fatih, Hashmi, Seema, Ulmer, Francis, Cleper, Roxanna, Ettenger, Robert, Antignac, Corinne, Wiggins, Roger C., Zenker, Martin, Hildebrandt, Friedhelm
Published in Nephrology, dialysis, transplantation (01.04.2008)
Published in Nephrology, dialysis, transplantation (01.04.2008)
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Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome
Boyer, Olivia, Benoit, Geneviève, Gribouval, Olivier, Nevo, Fabien, Pawtowski, Audrey, Bilge, Ilmay, Bircan, Zelal, Deschênes, Georges, Guay-Woodford, Lisa M, Hall, Michelle, Macher, Marie-Alice, Soulami, Kenza, Stefanidis, Constantinos J, Weiss, Robert, Loirat, Chantal, Gubler, Marie-Claire, Antignac, Corinne
Published in Journal of medical genetics (01.07.2010)
Published in Journal of medical genetics (01.07.2010)
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Rituximab therapy for childhood-onset systemic lupus erythematosus
Willems, M., Haddad, E., Niaudet, P., Koné-Paut, I., Bensman, A., Cochat, P., Deschênes, G., Fakhouri, F., Leblanc, T., Llanas, B., Loirat, C., Pillet, P., Ranchin, B., Salomon, R., Ulinski, T., Bader-Meunier, Brigitte
Published in The Journal of pediatrics (01.05.2006)
Published in The Journal of pediatrics (01.05.2006)
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The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts
Fremeaux-Bacchi, V, Kemp, E J, Goodship, J A, Dragon-Durey, M-A, Strain, L, Loirat, C, Deng, H-W, Goodship, T H J
Published in Journal of medical genetics (01.11.2005)
Published in Journal of medical genetics (01.11.2005)
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Abdominal manifestations in childhood-onset systemic lupus erythematosus
Richer, O, Ulinski, T, Lemelle, I, Ranchin, B, Loirat, C, Piette, J C, Pillet, P, Quartier, P, Salomon, R, Bader-Meunier, B
Published in Annals of the rheumatic diseases (01.02.2007)
Published in Annals of the rheumatic diseases (01.02.2007)
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Hemolytic and uremic syndrome and related thrombotic microangiopathies: Treatment and prognosis
Rafat, C, Coppo, P, Fakhouri, F, Frémeaux-Bacchi, V, Loirat, C, Zuber, J, Rondeau, E
Published in La revue de medecine interne (01.12.2017)
Published in La revue de medecine interne (01.12.2017)
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Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)
Veyradier, A., Lavergne, J‐M., Ribba, A‐S., Obert, B., Loirat, C., Meyer, D., Girma, J‐P.
Published in Journal of thrombosis and haemostasis (01.03.2004)
Published in Journal of thrombosis and haemostasis (01.03.2004)
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Hemolytic uremic syndrome due to Shiga toxin-producing Escherichia coli infection
Bruyand, M., Mariani-Kurkdjian, P., Gouali, M., de Valk, H., King, L.A., Le Hello, S., Bonacorsi, S., Loirat, C.
Published in Médecine et maladies infectieuses (01.05.2018)
Published in Médecine et maladies infectieuses (01.05.2018)
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Population pharmacokinetics of mycophenolic acid in kidney transplant pediatric and adolescent patients
Payen, S, Zhang, D, Maisin, A, Popon, M, Bensman, A, Bouissou, F, Loirat, C, Gomeni, R, Bressolle, F, Jacqz-Aigrain, E
Published in Therapeutic drug monitoring (01.06.2005)
Published in Therapeutic drug monitoring (01.06.2005)
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