Functional Assessment of Fatigue and Other Patient-Reported Outcomes in Patients Enrolled in the Global aHUS Registry

Autor: Ioannis Tomazos, Vasileios Nikolaou, Christoph Licht, Spero R. Cataland, Benjamin Miller, Christian S. Haas, Janet Green, Rita D. Swinford, Elena Román-Ortiz, Imad Al-Dakkak, Larry A. Greenbaum, Hae Il Cheong, Lisa Sartz

Publikováno v: Kidney International Reports. 5:1161-1171

Introduction Atypical hemolytic uremic syndrome (aHUS) is a progressive and potentially life-threatening disease characterized by complement-mediated thrombotic microangiopathy. Patients with aHUS may experience fatigue, which can negatively impact t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2a1099d0550b12711d7b35c5c13e160a
https://doi.org/10.1016/j.ekir.2020.05.003

Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome

Autor: Chantal Loirat, Gema Ariceta, Gianluigi Ardissino, Galina Generolova, Anne-Laure Lapeyraque, Christoph Gasteyger, Donata Cresseri, Åsa Lommelé, Franz Schaefer, Johan Vande Walle, Marie Scully, Lisa Sartz, Leena Martola, Daniel Landau, Patricia Hirt-Minkowski, Natalya Lvovna Kozlovskaya, Nicholas J.A. Webb, Michal Malina, Nicole M. Isbel, Eric Rondeau, Andrew M. Siedlecki, Larry A. Greenbaum, Masayo Ogawa, Fadi Fakhouri, Varant Kupelian, Christoph Licht, Annick Massart, Véronique Frémeaux-Bacchi, M. Blasco, Sally Johnson, Christoph J. Mache

Publikováno v: Kidney International. 94:408-418

Atypical hemolytic uremic syndrome (aHUS) is a rare, genetic, life-threatening disease. The Global aHUS Registry collects real-world data on the natural history of the disease. Here we characterize end-stage renal disease (ESRD)-free survival, the ra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5e81c1e692298c824e8476c8d3c87ad
https://doi.org/10.1016/j.kint.2018.02.029

Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort

Autor: Federico Baronio, Claudio La Scola, Constantinos J. Stefanidis, Jerzy Moczko, Hae Il Cheong, Jung Won Lee, Maria Szczepańska, Iga Załuska-Leśniewska, Franca Zurrida, Patrizia Fonduli, Magdalena Roszak, Valerie Said-Conti, Se Jin Park, Franca Anglani, Przemysław Sikora, Dariusz Runowski, Arend Bökenkamp, Lisa Sartz, Angela La Manna, Aleksandra Krzemień, Zoran Gucev, Detlef Bockenhauer, Julia Bürger, Dusan Paripovic, Fabio Paglialonga, Martin Konrad, Yo Han Ahn, Anna Wasilewska, Michael Ludwig, Anna Niemirska, Jutta Gellermann, Woo Yeong Chung, Yong Hoon Park, Maria Addis, Marcin Zaniew, Marcin Kołbuc, Grzegorz Siteń, Anna Rogowska-Kalisz, Rina Rus, Velibor Tasic, Argyroula Zampetoglou, Monika Miklaszewska

Publikováno v: Nephrology Dialysis Transplantation, 33(1), 85-94. Oxford University Press
Zaniew, M, Bökenkamp, A, Kołbuc, M, la Scola, C, Baronio, F, Niemirska, A, Szczepańska, M, Bürger, J, la Manna, A, Miklaszewska, M, Rogowska-Kalisz, A, Gellermann, J, Zampetoglou, A, Wasilewska, A, Roszak, M, Moczko, J, Krzemień, A, Runowski, D, Siteń, G, Załuska-Leśniewska, I, Fonduli, P, Zurrida, F, Paglialonga, F, Gucev, Z, Paripovic, D, Rus, R, Said-Conti, V, Sartz, L, Chung, W Y, Park, S J, Lee, J W, Park, Y H, Ahn, Y H, Sikora, P, Stefanidis, C J, Tasic, V, Konrad, M, Anglani, F, Addis, M, Cheong, H I, Ludwig, M & Bockenhauer, D 2018, ' Long-term renal outcome in children with OCRL mutations: Retrospective analysis of a large international cohort ', Nephrology Dialysis Transplantation, vol. 33, no. 1, pp. 85-94 . https://doi.org/10.1093/ndt/gfw350

Background. Lowe syndrome (LS) and Dent-2 disease (DD2) are disorders associated with mutations in the OCRL gene and characterized by progressive chronic kidney disease (CKD). Here, we aimed to investigate the long-term renal outcome and identify pot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b6dd5b3368dcd73f6f20e6fdd2b945
https://pubmed.ncbi.nlm.nih.gov/27708066

Complement activation on platelet-leukocyte complexes and microparticles in enterohemorrhagic Escherichia coli–induced hemolytic uremic syndrome

Autor: Anne-lie Ståhl, Diana Karpman, Lisa Sartz

Publikováno v: Blood; 117, pp 5503-5513 (2011)

Hemolytic uremic syndrome (HUS) is commonly associated with Shiga toxin (Stx)–producing Escherichia coli O157:H7 infection. This study examined patient samples for complement activation on leukocyte-platelet complexes and microparticles, as well as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a63f5c1a3291dd924fce8accad63b458
https://doi.org/10.1182/blood-2010-09-309161

An outbreak ofEscherichia coliO157:H7 infection in southern Sweden associated with consumption of fermented sausage; aspects of sausage production that increase the risk of contamination

Autor: H-B Hansson, E. Eriksson, B Osterman, L Plym-Forshell, Anne-lie Ståhl, Diana Karpman, Lisa Sartz, M Hjertqvist, S Lofdahl, R Alsterlund, B. de Jong

Publikováno v: Epidemiology and Infection. 136:370-380

SUMMARYA large outbreak of enterohaemorrhagicEscherichia coli(EHEC) infections occurred in southern Sweden during autumn 2002. A matched case-control study was performed and indicated an association between consumption of fermented sausage and EHEC i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58074822bde3a731a6c496235a12bda6
https://doi.org/10.1017/s0950268807008473