hemolytic uremic syndrome

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How I Treat Complement-Mediated TMA
C. John Sperati

CJASN March 2022, 17 (3) 452-454; DOI: https://doi.org/10.2215/CJN.13581021

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Infection in Patients with Suspected Thrombotic Microangiopathy Based on Clinical Presentation
Benjamin Thoreau, Florent von Tokarski, Adeline Bauvois, Guillaume Bayer, Christelle Barbet, Sylvie Cloarec, Elodie Mérieau, Sébastien Lachot, Denis Garot, Louis Bernard, Emmanuel Gyan, Franck Perrotin, Claire Pouplard, François Maillot, Philippe Gatault, Bénédicte Sautenet, Emmanuel Rusch, Véronique Frémeaux-Bacchi, Cécile Vigneau, Fadi Fakhouri and Jean-Michel Halimi

CJASN September 2021, 16 (9) 1355-1364; DOI: https://doi.org/10.2215/CJN.17511120

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Inherited Kidney Complement Diseases
Mathieu Lemaire, Damien Noone, Anne-Laure Lapeyraque, Christoph Licht and Véronique Frémeaux-Bacchi

CJASN June 2021, 16 (6) 942-956; DOI: https://doi.org/10.2215/CJN.11830720

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Monitoring Complement Activation
Fadi Fakhouri and Véronique Frémeaux-Bacchi

CJASN December 2019, 14 (12) 1682-1683; DOI: https://doi.org/10.2215/CJN.12111019

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Complement Gene Variants and Shiga Toxin–Producing Escherichia coli–Associated Hemolytic Uremic Syndrome
Véronique Frémeaux-Bacchi, Anne-Laure Sellier-Leclerc, Paula Vieira-Martins, Sophie Limou, Theresa Kwon, Annie Lahoche, Robert Novo, Brigitte Llanas, François Nobili, Gwenaëlle Roussey, Mathilde Cailliez, Tim Ulinski, Georges Deschênes, Corinne Alberti, François-Xavier Weill, Patricia Mariani and Chantal Loirat

CJASN March 2019, 14 (3) 364-377; DOI: https://doi.org/10.2215/CJN.05830518

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A Patient with Hemolytic Uremic Syndrome and Kidney Failure
Joshua M. Thurman

CJASN June 2018, 13 (6) 933-936; DOI: https://doi.org/10.2215/CJN.13191117

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Hemolytic Uremic Syndrome in Pregnancy and Postpartum
Alexandra Bruel, David Kavanagh, Marina Noris, Yahsou Delmas, Edwin K.S. Wong, Elena Bresin, François Provôt, Vicky Brocklebank, Caterina Mele, Giuseppe Remuzzi, Chantal Loirat, Véronique Frémeaux-Bacchi and Fadi Fakhouri

CJASN August 2017, 12 (8) 1237-1247; DOI: https://doi.org/10.2215/CJN.00280117

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Pathogenic Variants in Complement Genes and Risk of Atypical Hemolytic Uremic Syndrome Relapse after Eculizumab Discontinuation
Fadi Fakhouri, Marc Fila, François Provôt, Yahsou Delmas, Christelle Barbet, Valérie Châtelet, Cédric Rafat, Mathilde Cailliez, Julien Hogan, Aude Servais, Alexandre Karras, Raifah Makdassi, Feriell Louillet, Jean-Philippe Coindre, Eric Rondeau, Chantal Loirat and Véronique Frémeaux-Bacchi

CJASN January 2017, 12 (1) 50-59; DOI: https://doi.org/10.2215/CJN.06440616

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Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome
Caterina Mele, Mathieu Lemaire, Paraskevas Iatropoulos, Rossella Piras, Elena Bresin, Serena Bettoni, David Bick, Daniel Helbling, Regan Veith, Elisabetta Valoti, Roberta Donadelli, Luisa Murer, Maria Neunhäuserer, Matteo Breno, Véronique Frémeaux-Bacchi, Richard Lifton, Giuseppe Remuzzi and Marina Noris

CJASN June 2015, 10 (6) 1011-1019; DOI: https://doi.org/10.2215/CJN.08520814

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Factors Influencing Treatment of Atypical Hemolytic Uremic Syndrome
Carla M. Nester and Richard J.H. Smith

CJASN September 2014, 9 (9) 1516-1518; DOI: https://doi.org/10.2215/CJN.07540714

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