Transplant Outcomes in Patients with Idiopathic Membranous Nephropathy

Por Kennedy, Claire, Traynor, Carol, O'Kelly, Patrick, Dorman, Anthony, Conlon, Peter J.
Publicado em 2013

Kidney transplant outcomes in familial C3 glomerulopathy

Por Wong, Limy, Moran, Sarah, Lavin, Peter J., Dorman, Anthony M., Conlon, Peter J.
Publicado no Clin Kidney J (2016)

Recurrence of Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis in Appropriately Immunosuppressed Renal Transplant Patients: A Discussion of Two Cases

Por O'Brien, Frank J., Abdalla, Ahad, Wong, Limy, Traynor, Carol A., Cheriyan, Paul, Kok, Hong Kwan, Casserly, Liam, Dorman, Anthony, Conlon, Peter J.
Publicado em 2013

Comprehensive Investigation of the Caveolin 2 Gene: Resequencing and Association for Kidney Transplant Outcomes

Por McCaughan, Jennifer A., Duffy, Seamus, O'Hagan, Thomas, Courtney, Aisling E., Borrows, Richard, Conlon, Peter J., Maxwell, Alexander P., McKnight, Amy Jayne
Publicado em 2013

Re-infection following sustained virological response with a different hepatitis C virus genotype: implications for infection control policy

Por O'Shaughnessy, Michelle M., O'Regan, John A., Murray, Frank E., Connell, Jeff A., Duffy, Margaret P., Francis, Veronica M., Dwyer, Sharon, Thornton, Lelia M., Conlon, Peter J.
Publicado no Clin Kidney J (2012)

Arterio-venous fistula buttonhole cannulation technique: a retrospective analysis of infectious complications

Por O'Brien, Frank J., Kok, Hong Kuan T., O'Kane, Claire, McWilliams, Johanna, O'Kelly, Patrick, Collins, Paula, Walshe, Joseph, Magee, Colm C., Denton, Mark D., Conlon, Peter J.
Publicado no Clin Kidney J (2012)

A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy

Por Malik, Talat H., Lavin, Peter J., Goicoechea de Jorge, Elena, Vernon, Katherine A., Rose, Kirsten L., Patel, Mitali P., de Leeuw, Marcel, Neary, John J., Conlon, Peter J., Winn, Michelle P., Pickering, Matthew C.
Publicado em 2012

C3 Glomerulopathy: Clinicopathologic Features and Predictors of Outcome

Por Medjeral-Thomas, Nicholas R., O’Shaughnessy, Michelle M., O’Regan, John A., Traynor, Carol, Flanagan, Michael, Wong, Limy, Teoh, Chia Wei, Awan, Atif, Waldron, Mary, Cairns, Tom, O’Kelly, Patrick, Dorman, Anthony M., Pickering, Matthew C., Conlon, Peter J., Cook, H. Terence
Publicado em 2014

A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

Por Hall, Gentzon, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Liu, Yangfan, Oh, Edwin C., Wang, Liming, Spurney, Robert F., Eckel, Jason, Lindsey, Thomas, Homstad, Alison, Malone, Andrew F., Phelan, Paul J., Shaw, Andrey, Howell, David N., Conlon, Peter J., Katsanis, Nicholas, Winn, Michelle P.
Publicado no J Am Soc Nephrol (2015)

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

Por Malone, Andrew F, Phelan, Paul J, Hall, Gentzon, Cetincelik, Umran, Homstad, Alison, Alonso, Andrea, Jiang, Ruiji, Lindsey, Thomas, Wu, Guanghong, Sparks, Matthew A, Smith, Stephen R, Webb, Nicholas J A, Kalra, Philip, Adeyemo, Adebowale, Shaw, Andrey S, Conlon, Peter J, Jennette, J Charles, Howell, David N, Winn, Michelle P, Gbadegesin, Rasheed A
Publicado no Kidney Int (2014)