Increased renal allograft thrombosis in CAPD patients von MURPHY, B. G, HILL, C. M, MIDDLETON, D, DOHERTY, C. C, BROWN, J. H, NELSON, W. E, KERNOHAN, R. M, KEANE, P. K, DOUGLAS, J. F, MCNAMEE, P. T

Volltext

Migration of Filshie clips--report of two cases and review of the literature von Connolly, D, McGookin, R R, Wali, J, Kernohan, R M

Volltext

A controlled trial of bipolar electrocoagulation in patients with upper gastrointestinal bleeding von Kernohan, R. M., Anderson, J. R., McKelvey, S. T. D., Kennedy, T. L.

Volltext

Squamous cell carcinoma of the bladder and prostatic urethra in a post renal transplant patient von Nambirajan, T, Woolsey, S, Mahendra, V, O'Rourke, D, Walsh, I K, Kernohan, R M

Volltext

Closed abdominal trauma in a child causing avulsion of the common bile duct and gastric stasis von Kernohan, R.M., Humphreys, W.G.

Volltext

Does cholecystectomy predispose to colorectal cancer? A case control study von Moorehead, R J, Kernohan, R M, Patterson, C C, McKelvey, S T, Parks, T G

Volltext

The artificial urinary sphincter. A new solution for incontinent patients von Keane, P F, Walsh, I K, Kernohan, R M

Volltext

Laser lithotripsy for ureteric calculi: results in 250 patients von Kelly, J D, Keane, P F, Johnston, S R, Kernohan, R M

Volltext

Increased renal allograft thrombosis in CAPD patients von Murphy, B. G., Hill, C. M., Middleton, D., Doherty, C. C., Brown, J. H., Nelson, W. E., Kernohan, R. M., Keane, P. K., Douglas, J. F., McNamee, P. T.

Volltext

Does cholecystectomy predispose to colorectal cancer? von MOOREHEAD, R. J, KERNOHAN, R. M, PATTERSON, C. C, MCKELVEY, S. T. D, PARKS, T. G

Volltext

New Diagnostic Approaches for Undiagnosed Rare Genetic Diseases von Hartley, Taila, Lemire, Gabrielle, Kernohan, Kristin D, Howley, Heather E, Adams, David R, Boycott, Kym M

Volltext

Phenformin as prophylaxis and therapy in breast cancer xenografts von Appleyard, M V C L, Murray, K E, Coates, P J, Wullschleger, S, Bray, S E, Kernohan, N M, Fleming, S, Alessi, D R, Thompson, A M

Volltext

Compound heterozygous variants in SHQ1 are associated with a spectrum of neurological features, including early-onset dystonia von Sleiman, Sophie, Marshall, Aren E, Dong, Xiaomin, Mhanni, Aziz, Alidou-D’Anjou, Ismaël, Frosk, Patrick, Marin, Samantha E, Stark, Zornitza, Del Bigio, Marc R, McBride, Arran, Sadedin, Simon, Gallacher, Lyndon, Christodoulou, John, Boycott, Kym M, Dragon, François, Kernohan, Kristin D

Volltext

Toric intraocular lens versus limbal relaxing incisions for corneal astigmatism after phacoemulsification von Lake, Jonathan C, Victor, Gustavo, Clare, Gerry, Porfírio, Gustavo JM, Kernohan, Ashleigh, Evans, Jennifer R, Lake, Jonathan C

Volltext

Long‐read genome sequencing reveals a novel intronic retroelement insertion in NR5A1 associated with 46,XY differences of sexual development von Del Gobbo, Giulia F., Wang, Xueqi, Couse, Madeline, Mackay, Layla, Goldsmith, Claire, Marshall, Aren E., Liang, Yijing, Lambert, Christine, Zhang, Siyuan, Dhillon, Harsharan, Fanslow, Cairbre, Rowell, William J., Marshall, Christian R., Kernohan, Kristin D., Boycott, Kym M.

Volltext

Genomics4RD: An integrated platform to share Canadian deep‐phenotype and multiomic data for international rare disease gene discovery von Driver, Hannah G., Hartley, Taila, Price, E. Magda, Turinsky, Andrei L., Buske, Orion J., Osmond, Matthew, Ramani, Arun K., Kirby, Emily, Kernohan, Kristin D., Couse, Madeline, Elrick, Hillary, Lu, Kevin, Mashouri, Pouria, Mohan, Aarthi, So, Delvin, Klamann, Conor, Le, Hannah G. B. H., Herscovich, Andrea, Marshall, Christian R., Statia, Andrew, Canada Consortium, Care4Rare, Knoppers, Bartha M., Brudno, Michael, Boycott, Kym M.

Volltext

Phenotypic heterogeneity associated with KIF21A: Two new cases and review of the literature von Bhola, Priya T., Mishra, Radha, Posey, Jennifer E., Hamilton, Leslie E., Graham, Gail E., Punetha, Jaya, Lupski, James R., Boycott, Kym M., D'Amours, Damien, Kernohan, Kristin D.

Volltext

Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxia von Zambonin, Jessica L, Bellomo, Allison, Ben-Pazi, Hilla, Everman, David B, Frazer, Lee M, Geraghty, Michael T, Harper, Amy D, Jones, Julie R, Kamien, Benjamin, Kernohan, Kristin, Koenig, Mary Kay, Lines, Matthew, Palmer, Elizabeth Emma, Richardson, Randal, Segel, Reeval, Tarnopolsky, Mark, Vanstone, Jason R, Gibbons, Melissa, Collins, Abigail, Fogel, Brent L, Dudding-Byth, Tracy, Boycott, Kym M

Volltext

An unusual extranodal T-cell non-Hodgkin lymphoma von Coats, Josh T, MRCP, Mackie, Alasdair D R, MD, Kernohan, Neil M, PhD, Ramkumar, Prasad Guntur, FRCR, McMahon, Lesley M, PhD, Goodlad, John R, MD, Tauro, Sudhir, Dr

Volltext

Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy von McMillan, Hugh J., Marshall, Aren E., Venkateswaran, Sunita, Hartley, Taila, Warman‐Chardon, Jodi, Ramani, Arun K., Marshall, Christian R., Michaud, Jean, Boycott, Kym M., Dyment, David A., Kernohan, Kristin D.

Volltext