P. Walsh

发表

Treatment and management of children with haemolytic uraemic syndrome

S. Johnson, P. Walsh, Sally Johnson, 2017, Archives of Disease in Childhood.

Clinical and diagnostic features of Bartter and Gitelman syndromes

R. Kleta, D. Bockenhauer, L. Jenkins, 2017, Clinical kidney journal.

Glucose-6-Phosphate Dehydrogenase Deficiency Mimicking Atypical Hemolytic Uremic Syndrome.

D. Kavanagh, S. Johnson, P. Walsh, 2017, American journal of kidney diseases : the official journal of the National Kidney Foundation.

New insights into risk factors for transplant-associated thrombotic microangiopathy in pediatric HSCT.

G. Lucchini, A. Gennery, S. Annavarapu, 2020, Blood advances.

Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome

N. Sheerin, D. Kavanagh, S. Johnson, 2022, Transplantation.

Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland

R. Gilbert, N. Sheerin, A. Salama, 2017, Kidney international.

Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing

B. McNicholas, C. Becker, P. Nürnberg, 2022 .

Complement receptor CD46 co-stimulates optimal human CD8+ T cell effector function via fatty acid metabolism

M. Pirooznia, I. Tunc, D. Kavanagh, 2018, Nature Communications.

Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy

D. Milford, D. Gale, N. Sheerin, 2020, Kidney international.

The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes

Colin A. Johnson, M. Hubank, E. Stupka, 2015, Journal of Medical Genetics.

Erratum: The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes

Colin A. Johnson, M. Hubank, E. Stupka, 2016, Journal of Medical Genetics.

None fits all: Unraveling structural rearrangements of the CFH gene cluster in aHUS patients using molecular combing and long fragment targeted sequencing.

B. McNicholas, C. Becker, P. Nürnberg, 2022, The Journal of molecular diagnostics : JMD.

Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD

P. Barlow, D. Kavanagh, C. Harris, 2021, Frontiers in Immunology.

Clinical and molecular aspects of distal renal tubular acidosis in children

R. Kleta, D. Bockenhauer, L. Jenkins, 2017, Pediatric Nephrology.

Eculizumab in the treatment of Shiga toxin haemolytic uraemic syndrome

S. Johnson, P. Walsh, Sally Johnson, 2018, Pediatric Nephrology.

Complement receptor CD46 co-stimulates optimal human CD8+ T cell effector function via fatty acid metabolism

M. Pirooznia, I. Tunc, D. Kavanagh, 2018, Nature Communications.