檢索結果 - Lemaire, Mathieu

Treatment for otitis media 由 Lemaire, Mathieu

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

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

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

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

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

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

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A novel disease-causing mutation in AVPR2: Q96H 由 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. 由 Li, Qi, Gulati, Ashima, Lemaire, Mathieu, Nottoli, Timothy, Bale, Allen, Tufro, Alda

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

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Diacylglycerol Kinase-ε: Properties and Biological Roles 由 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 由 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 由 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 由 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... 由 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 由 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 由 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 由 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 由 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 由 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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