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Authors
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Year

Regulation of complement activation of surfaces ::towards better understanding of atypical hemolytic uremic syndrome

Hyvärinen, Satu
[S. Hyvärinen]2016

Better late than never:Diagnosis of recurrent atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.5414/CN111047
Aaltonen, Sari; Räisänen-Sokolowski, Anne; Kaartinen, Kati
Clinical nephrology2023

Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in children: incidence, risk factors, and clinical outcome

Peer-reviewed
Open access
DOI
10.1007/s00467-020-04560-0
Ylinen, Elisa; Salmenlinna, Saara; Halkilahti, Jani; Jahnukainen, Timo; Korhonen, Linda; Virkkala, T...
Pediatric nephrology2020

Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1016/j.molimm.2015.12.005
Nozal, Pilar; Bernabeu-Herrero, Maria E.; Uzonyi, Barbara; Szilagyi, Agnes; Hyvarinen, Satu; Prohasz...
Molecular immunology2016

Comparative Genomics of Shiga Toxin-Producing Escherichia coli Strains Isolated from Pediatric Patients with and without Hemolytic Uremic Syndrome from 2000 to 2016 in Finland

Peer-reviewed
Open access
DOI
10.1128/spectrum.00660-22
Bai, Xiangning; Ylinen, Elisa; Zhang, Ji; Salmenlinna, Saara; Halkilahti, Jani; Saxen, Harri; Naraya...
Microbiology spectrum2022

Analysis of Linear Antibody Epitopes on Factor H and CFHR1 Using Sera of Patients with Autoimmune Atypical Hemolytic Uremic Syndrome

Peer-reviewed
Open access
DOI
10.3389/fimmu.2017.00302
Trojnar, Eszter; Jozsi, Mihaly; Uray, Katalin; Csuka, Dorottya; Szilagyi, Agnes; Milosevic, Danko; S...
Frontiers in immunology2017

Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1182/blood-2014-10-609073
Schramm, Elizabeth C.; Roumenina, Lubka T.; Rybkine, Tania; Chauvet, Sophie; Vieira-Martins, Paula; ...
Blood2015

Complement Activation During Liver Transplantation-Special Emphasis on Patients With Atypical Hemolytic Uremic Syndrome

Peer-reviewed
DOI
10.1111/j.1600-6143.2011.03612.x
Koskinen, A. R.; Tukiainen, Erkki Juhani; Arola, J.; Nordin, Arno; Höckerstedt, Krister; Nilsson, B....
American journal of transplantation2011

Disturbed sialic acid recognition on endothelial cells and platelets in complement attack causes atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1182/blood-2015-11680009
Hyvarinen, Satu; Meri, Seppo; Jokiranta, T. Sakari
Blood2016

Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum

Peer-reviewed
Open access
DOI
10.1016/j.kint.2024.09.012
Kavanagh, David; Ardissino, Gianluigi; Brocklebank, Vicky; Bouwmeester, Romy N.; Bagga, Arvind; ter ...
Kidney international2024

Regulation of complement activation of surfaces ::towards better understanding of atypical hemolytic uremic syndrome

2016

Better late than never:Diagnosis of recurrent atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.5414/CN111047
2023

Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in children: incidence, risk factors, and clinical outcome

Peer-reviewed
Open access
DOI
10.1007/s00467-020-04560-0
2020

Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1016/j.molimm.2015.12.005
2016

Comparative Genomics of Shiga Toxin-Producing Escherichia coli Strains Isolated from Pediatric Patients with and without Hemolytic Uremic Syndrome from 2000 to 2016 in Finland

Peer-reviewed
Open access
DOI
10.1128/spectrum.00660-22
2022

Analysis of Linear Antibody Epitopes on Factor H and CFHR1 Using Sera of Patients with Autoimmune Atypical Hemolytic Uremic Syndrome

Peer-reviewed
Open access
DOI
10.3389/fimmu.2017.00302
2017

Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1182/blood-2014-10-609073
2015

Complement Activation During Liver Transplantation-Special Emphasis on Patients With Atypical Hemolytic Uremic Syndrome

Peer-reviewed
DOI
10.1111/j.1600-6143.2011.03612.x
2011

Disturbed sialic acid recognition on endothelial cells and platelets in complement attack causes atypical hemolytic uremic syndrome

Peer-reviewed
DOI
10.1182/blood-2015-11680009
2016

Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International Forum

Peer-reviewed
Open access
DOI
10.1016/j.kint.2024.09.012
2024