Search Results - Lemaire, Mathieu

Treatment for otitis media by Lemaire, Mathieu

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On the Importance of Considering Glycosylation When Evaluating Biologic Therapies by Lemaire, Mathieu

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A Perspective on Inherited Kidney Disease: Lessons for Practicing Nephrologists by Lemaire, Mathieu, Parekh, Rulan S.

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Rapid Tumor Cell Swelling and Bursting: Beware of Collateral Damage by Lemaire, Mathieu, Halperin, Mitchell L

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Reappraising suppression: subjective and physiological correlates of experiential suppression in healthy adults by Lemaire, Mathieu, El-Hage, Wissam, Frangou, Sophia

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Opportunities and Challenges for Genetic Studies of End-Stage Renal Disease in Canada by Kalatharan, Vinusha, Lemaire, Mathieu, Lanktree, Matthew B.

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Treatment of paediatric vancomycin intoxication: a case report and review of the literature by Lemaire, Mathieu, Connolly, Bairbre, Harvey, Elizabeth, Licht, Christoph

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A novel disease-causing mutation in AVPR2: Q96H by Lemaire, Mathieu, Chitayat, David, Geary, Denis F., Bichet, Daniel G., Licht, Christoph

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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

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Inherited Kidney Complement Diseases by Lemaire, Mathieu, Noone, Damien, Lapeyraque, Anne-Laure, Licht, Christoph, Frémeaux-Bacchi, Véronique

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Diacylglycerol Kinase-ε: Properties and Biological Roles by Epand, Richard M., So, Vincent, Jennings, William, Khadka, Bijendra, Gupta, Radhey S., Lemaire, Mathieu

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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

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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

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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

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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

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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

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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

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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

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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

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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.

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