Atypical hemolytic uremic syndrome: Unique clinical presentation linked to rare CFHR5 mutation-Reference-Cited by-同舟云学术

Atypical hemolytic uremic syndrome: Unique clinical presentation linked to rare CFHR5 mutation

Published:2021-09-14 Issue:4 Volume:2 Page:838-841
ISSN:2688-6146
Container-title:eJHaem
language:en
Short-container-title:eJHaem

Author:

Menotti Sofia¹,Donini Martino¹,Pessolano Giuseppina¹,Tiro Livia¹,Cantini Maurizio²,Croce Jacopo¹,Morandi Matteo¹,Mazzi Filippo¹,Donadello Katia³,Olivieri Oliviero¹,Dima Francesco⁴,De Marchi Sergio¹,Gambaro Giovanni¹,Polati Enrico³,De Franceschi Lucia¹^ORCID

Affiliation:

1. Department of Medicine University of Verona and AOUI Verona Verona Italy

2. Department of Transfusion Medicine University Hospital Verona Italy

3. Department of Neuroscience, Biomedicine and Movement, Section of Clinical Biochemistry University of Verona and AOUI Verona Italy

4. Department of Surgery, Dentistry, Paediatrics and Gynaecology University of Verona & AOUI Verona Italy

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jha2.288

Reference14 articles.

1. Thrombotic microangiopathy in aHUS and beyond: clinical clues from complement genetics

2. Profiles of Coagulation and Fibrinolysis Activation-Associated Molecular Markers of Atypical Hemolytic Uremic Syndrome in the Acute Phase

3. VWF excess and ADAMTS13 deficiency: a unifying pathomechanism linking inflammation to thrombosis in DIC, malaria, and TTP

4. Eculizumab discontinuation in children and adults with atypical hemolytic-uremic syndrome: a prospective multicenter study

5. Terminal Complement Inhibitor Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome: A Single-Arm, Open-Label Trial

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