Patrick R. Walsh
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Properdin deficiency or anti-properdin treatment ameliorates disease in the C3 gain-of-function mouse model of atypical haemolytic uraemic syndrome.
Journal: Frontiers in immunology
Published: March 11, 2026
Biallelic pathogenic variants in EXOSC3 mediate renal thrombotic microangiopathy of the kidney.
Journal: Kidney international
Published: February 10, 2026
Atypical hemolytic uremic syndrome.
Journal: The Journal of allergy and clinical immunology
Published: January 31, 2025
The role of complement factor I rare genetic variants in age related macular degeneration in Finland.
Journal: Human molecular genetics
Published: May 09, 2024
Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing.
Journal: The Journal of molecular diagnostics : JMD
Published: November 16, 2021
Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
Journal: Frontiers in immunology
Published: September 02, 2020
New insights into risk factors for transplant-associated thrombotic microangiopathy in pediatric HSCT.
Journal: Blood advances
Published: December 06, 2019
Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy.
Journal: Kidney international
Published: November 14, 2019
Complement receptor CD46 co-stimulates optimal human CD8+ T cell effector function via fatty acid metabolism.
Journal: Nature communications
Published: January 25, 2018
Last Updated: 09/26/2026