Treatment for otitis media

by Lemaire, Mathieu
Published 2005

A Perspective on Inherited Kidney Disease: Lessons for Practicing Nephrologists

by Lemaire, Mathieu, Parekh, Rulan S.
Published in Clin J Am Soc Nephrol (2017)

Rapid Tumor Cell Swelling and Bursting: Beware of Collateral Damage

by Lemaire, Mathieu, Halperin, Mitchell L
Published 2009

Reappraising suppression: subjective and physiological correlates of experiential suppression in healthy adults

by Lemaire, Mathieu, El-Hage, Wissam, Frangou, Sophia
Published 2014

Opportunities and Challenges for Genetic Studies of End-Stage Renal Disease in Canada

by Kalatharan, Vinusha, Lemaire, Mathieu, Lanktree, Matthew B.
Published in Can J Kidney Health Dis (2018)

Treatment of paediatric vancomycin intoxication: a case report and review of the literature

by Lemaire, Mathieu, Connolly, Bairbre, Harvey, Elizabeth, Licht, Christoph
Published in NDT Plus (2010)

A novel disease-causing mutation in AVPR2: Q96H

by Lemaire, Mathieu, Chitayat, David, Geary, Denis F., Bichet, Daniel G., Licht, Christoph
Published in NDT Plus (2009)

Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis.

by Li, Qi, Gulati, Ashima, Lemaire, Mathieu, Nottoli, Timothy, Bale, Allen, Tufro, Alda
Published in Kidney Int (2021)

Inherited Kidney Complement Diseases

by Lemaire, Mathieu, Noone, Damien, Lapeyraque, Anne-Laure, Licht, Christoph, Frémeaux-Bacchi, Véronique
Published in Clin J Am Soc Nephrol (2021)

Diacylglycerol Kinase-ε: Properties and Biological Roles

by Epand, Richard M., So, Vincent, Jennings, William, Khadka, Bijendra, Gupta, Radhey S., Lemaire, Mathieu
Published in Front Cell Dev Biol (2016)

Driving Medical Innovation Through Interdisciplinarity: Unique Opportunities and Challenges

by Gohar, Faekah, Maschmeyer, Patrick, Mfarrej, Bechara, Lemaire, Mathieu, Wedderburn, Lucy R., Roncarolo, Maria Grazia, van Royen-Kerkhof, Annet
Published in Front Med (Lausanne) (2019)

Atypical Brain Mechanisms of Prediction According to Uncertainty in Autism

by Thillay, Alix, Lemaire, Mathieu, Roux, Sylvie, Houy-Durand, Emmanuelle, Barthélémy, Catherine, Knight, Robert T., Bidet-Caulet, Aurélie, Bonnet-Brilhault, Frédérique
Published in Front Neurosci (2016)

Management of Severe Hyponatremia With a Custom Continuous Renal Replacement Therapy in an Infant With Newly Diagnosed Chronic Kidney Disease

by Gaudreault-Tremblay, Marie-Michèle, Faqeehi, Hassan, Langlois, Valérie, Hébert, Diane, Parra, Dimitri A., Annich, Gail, Harvey, Elizabeth, Lemaire, Mathieu
Published in Kidney Int Rep (2017)

Management of Canadian Pediatric Patients With Glomerular Diseases During the COVID-19 Pandemic: Recommendations From the Canadian Association of Pediatric Nephrologists COVID-19 R...

by Robinson, Cal, Ruhl, Michelle, Kirpalani, Amrit, Alabbas, Abdullah, Noone, Damien, Teoh, Chia Wei, Langlois, Valerie, Phan, Veronique, Lemaire, Mathieu, Chanchlani, Rahul
Published in Can J Kidney Health Dis (2020)

The Phenotypic Spectrum of Tuberous Sclerosis Complex: A Canadian Cohort

by Alsowat, Daad, Whitney, Robyn, Hewson, Stacy, Jain, Puneet, Chan, Valerie, Kabir, Nadia, Amburgey, Kimberly, Noone, Damien, Lemaire, Mathieu, McCoy, Blathnaid, Zak, Maria
Published in Child Neurol Open (2021)

Canadian Association of Paediatric Nephrologists COVID-19 Rapid Response: Guidelines for Management of Acute Kidney Injury in Children

by Alabbas, Abdullah, Kirpalani, Amrit, Morgan, Catherine, Mammen, Cherry, Licht, Christoph, Phan, Veronique, Wade, Andrew, Harvey, Elizabeth, Zappitelli, Michael, Clark, Edward G., Hiremath, Swapnil, Soroka, Steven D., Wald, Ron, Weir, Matthew A., Chanchlani, Rahul, Lemaire, Mathieu
Published in Can J Kidney Health Dis (2021)

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome

by Mele, Caterina, Lemaire, Mathieu, Iatropoulos, Paraskevas, Piras, Rossella, Bresin, Elena, Bettoni, Serena, Bick, David, Helbling, Daniel, Veith, Regan, Valoti, Elisabetta, Donadelli, Roberta, Murer, Luisa, Neunhäuserer, Maria, Breno, Matteo, Frémeaux-Bacchi, Véronique, Lifton, Richard, Remuzzi, Giuseppe, Noris, Marina
Published in Clin J Am Soc Nephrol (2015)

The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε

by Azukaitis, Karolis, Simkova, Eva, Majid, Mohammad Abdul, Galiano, Matthias, Benz, Kerstin, Amann, Kerstin, Bockmeyer, Clemens, Gajjar, Radha, Meyers, Kevin E., Cheong, Hae Il, Lange-Sperandio, Bärbel, Jungraithmayr, Therese, Frémeaux-Bacchi, Véronique, Bergmann, Carsten, Bereczki, Csaba, Miklaszewska, Monika, Csuka, Dorottya, Prohászka, Zoltán, Gipson, Patrick, Sampson, Matthew G., Lemaire, Mathieu, Schaefer, Franz
Published in J Am Soc Nephrol (2017)

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

by Lemaire, Mathieu, Frémeaux-Bacchi, Véronique, Schaefer, Franz, Choi, Murim, Tang, Wai Ho, Le Quintrec, Moglie, Fakhouri, Fadi, Taque, Sophie, Nobili, François, Martinez, Frank, Ji, Weizhen, Overton, John D., Mane, Shrikant M., Nürnberg, Gudrun, Altmüller, Janine, Thiele, Holger, Morin, Denis, Deschenes, Georges, Baudouin, Véronique, Llanas, Brigitte, Collard, Laure, Majid, Mohammed A., Simkova, Eva, Nürnberg, Peter, Rioux-Leclerc, Nathalie, Moeckel, Gilbert W., Gubler, Marie Claire, Hwa, John, Loirat, Chantal, Lifton, Richard P.
Published 2013

SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes

by Kim, Jung-Hyun, Park, Eun Young, Chitayat, David, Stachura, David L., Schaper, Jörg, Lindstrom, Kristin, Jewett, Tamison, Wieczorek, Dagmar, Draaisma, Jos M., Sinnema, Margje, Hoeberigs, Christianne, Hempel, Maja, Bachman, Kristine K., Seeley, Andrea H., Stone, Joshua K., Kong, Hyun Kyung, Vukadin, Lana, Richard, Alexander, Shinde, Deepali N., McWalter, Kirsty, Si, Yue Cindy, Douglas, Ganka, Lim, Ssang-Taek Steve, Vissers, Lisenka E.L.M., Lemaire, Mathieu, Ahn, Eun-Young Erin
Published in Kidney Int (2019)