The directors of resident support program: a program evaluation of a resident well-being and support innovation von Ruzycki, Shannon M, des Ordons, Amanda Roze, Davis, Melinda, Steele, J MacGregor, Tutu, Kannin Osei, Welikovitch, Lisa

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P302: Decoding genetic orchestration: Understanding the cellular and molecular mechanisms of the hematopoietic failure in Fanconi anemia von Photi-A, Apichat, Benicio, Mariana, Li, Hongbing, Moshiri, Houtan, Armstrong, Richard, Sahinoglu, Efe, Breakey, Vickey, Abhish, Sharon, Villeneuve, Stephanie, Sinha, Roona, Corriveau-Bourque, Catharine, Steele, MacGregor, Dror, Yigal

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The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes von Cada, Michaela, Segbefia, Catherin I, Klaassen, Robert, Fernandez, Conrad V, Yanofsky, Rochelle A, Wu, John, Pastore, Yves, Silva, Mariana, Lipton, Jeffrey H, Brossard, Josee, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark, Breakey, Vicky, Jardine, Lawrence, Goodyear, Lisa, Sung, Lillian, Shago, Mary, Beyene, Joseph, Sharma, Preeti, Zlateska, Bozana, Dror, Yigal

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Magnetic resonance imaging in boys with severe hemophilia A: Serial and end‐of‐study findings from the Canadian Hemophilia Primary Prophylaxis Study von Stimec, Jennifer, Dover, Saunya, Pullenayegum, Eleanor, Blanchette, Victor S., Doria, Andrea S., Feldman, Brian M., Carcao, Manuel, Rivard, Georges E., Israels, Sara J., Chan, Anthony K., Steele, MacGregor, Cloutier, Stephanie, Klaassen, Robert J., Price, Victoria E., Sinha, Roona, Laferriere, Nicole, Paradis, Elizabeth, Wu, John K.M., Babyn, Paul

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Hemophilia prophylaxis adherence and bleeding using a tailored, frequency‐escalated approach: The Canadian Hemophilia Primary Prophylaxis Study von Dover, Saunya, Blanchette, Victor S., Wrathall, Darius, Pullenayegum, Eleanor, Kazandjian, Daniel, Song, Byron, Hawes, Sue Ann, Cloutier, Stéphanie, Rivard, Geroges E., Klaassen, Robert J., Paradis, Elizabeth, Laferriere, Nicole, Stain, Ann Marie, Chan, Anthony K., Israels, Sara J., Sinha, Roona, Steele, MacGregor, Wu, John K.M., Feldman, Brian M.

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Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels von Lauhasurayotin, Supanun, Cuvelier, Geoff D., Klaassen, Robert J., Fernandez, Conrad V., Pastore, Yves D., Abish, Sharon, Rayar, Meera, Steele, MacGregor, Jardine, Lawrence, Breakey, Vicky R., Brossard, Josee, Sinha, Roona, Silva, Mariana, Goodyear, Lisa, Lipton, Jeffrey H., Michon, Bruno, Corriveau-Bourque, Catherine, Sung, Lillian, Shabanova, Iren, Li, Hongbing, Zlateska, Bozana, Dhanraj, Santhosh, Cada, Michaela, Scherer, Stephen W., Dror, Yigal

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Childhood Autoimmune Hemolytic Anemia: A Scoping Review von Zhang, Caseng, Charland, Danielle, O'Hearn, Katie, Steele, MacGregor, Klaassen, Robert J., Speckert, Matthew

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Childhood autoimmune hemolytic anemia: A scoping review von Zhang, Caseng, Charland, Danielle, O'Hearn, Katie, Steele, MacGregor, Klaassen, Robert J., Speckert, Matthew

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The clinical impact of copy number variants in inherited bone marrow failure syndromes von Waespe, Nicolas, Dhanraj, Santhosh, Wahala, Manju, Tsangaris, Elena, Enbar, Tom, Zlateska, Bozana, Li, Hongbing, Klaassen, Robert J., Fernandez, Conrad V., Cuvelier, Geoff D. E., Wu, John K., Pastore, Yves D., Silva, Mariana, Lipton, Jeffrey H., Brossard, Joseé, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark J., Breakey, Vicky R., Jardine, Lawrence, Goodyear, Lisa, Kofler, Liat, Cada, Michaela, Sung, Lillian, Shago, Mary, Scherer, Stephen W., Dror, Yigal

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A post hoc analysis of PROTECT VIII kids assessing long-term efficacy and safety of damoctocog alfa pegol in adolescents with severe haemophilia A von Ahuja, Sanjay, Biss, Tina, Maas Enriquez, Monika, Mancuso, Maria Elisa, Steele, MacGregor, Kenet, Gili

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Mechanisms of defective erythropoiesis and anemia in pediatric acute lymphoblastic leukemia (ALL) von Steele, MacGregor, Narendran, Aru

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Long-Term Follow-up of Patients with Congenital Thrombotic Thrombocytopenia Purpura Receiving Plasma-Derived Factor VIII Containing (Koate®) von Chrisentery-Singleton, Tammuella, Boggio, Lisa N, Carcao, Manuel, Ibrahimi, Sami, Khan, Osman, Mahajerin, Arash, Rajasekhar, Anita, Sharma, Vivek, Steele, MacGregor, Torres, Marcela, Carpenter, Shannon L

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BAY 94-9027 Provides Safe and Effective Long-Term Prophylaxis in Pediatric Patients: Results from the PROTECT VIII Kids Extension Study von Ahuja, Sanjay, Fischer, Kathelijn, Biss, Tina, Maas Enriquez, Monika, Mancuso, Maria-Elisa, Steele, MacGregor, Wang, Maria, Kenet, Gili

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PROTECT VIII Kids: BAY 94-9027 (PEGylated Recombinant Factor VIII) safety and efficacy in previously treated children with severe haemophilia A von Santagostino, Elena, Kenet, Gili, Fischer, Kathelijn, Biss, Tina, Ahuja, Sanjay, Steele, MacGregor

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TINF2 Mutations Are Associated with Poor Outcome Post Hematopoietic Stem Cell Transplantation for Dyskeratosis Congenita von Lim, Yeon Jung, Arbiv, Omri Avraham, Kalbfleisch, Melanie Evelyn, Nuaimi, Mohammed, Steele, MacGregor, Cuvelier, Geoff D.E., Schechter-Finkelstein, Tal, Zlateska, Bozana, Cada, Michaela, Dror, Yigal

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Lack of an Alberta Newborn Screening Program Is Associated with Delayed Diagnosis of Sickle Cell Disease von Monagel, Dania, Leaker, Michael, Le, Doan, Wright, Nicola A., Ruzycki, Angela, Steele, MacGregor

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68 LRBA dysfunction: a new diagnostic entity caused by biallelic LRBA missense variants results in reduced CTLA-4 expression and autoimmunity von Chiang, Samuel, Murguia-Favela, Luis, Wright, Nicola, Steele, MacGregor, Seroogy, Christine, Blanchard-Rohner, Geraldine, Shrikhande, Anitha, Wilson, Jo, Yang, Li, Owsley, Erika, Hartog, Nicholas, Elizalde, Araceli, Bleesing, Jack, Dimitriades, Victoria, Gutierrez, Maria Jimena, Peng, Xiao, Derfalvi, Beata, Brager, Rae, Jordan, Michael, Marwaha, Ashish

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Vitamin B 12 Deficiency in Infancy: The Case for Screening von Singh, Gurpreet, Le, Doan, Schnabl, Kareena, Leaker, Michael T., Steele, MacGregor, Sparkes, Rebecca L.

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Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes von Ghemlas, Ibrahim, Li, Hongbing, Zlateska, Bozana, Klaassen, Robert, Fernandez, Conrad V, Yanofsky, Rochelle A, Wu, John, Pastore, Yves, Silva, Mariana, Lipton, Jeff H, Brossard, Josee, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark, Breakey, Vicky R, Jardine, Lawrence, Goodyear, Lisa, Sung, Lillian, Dhanraj, Santhosh, Reble, Emma, Wagner, Amanda, Beyene, Joseph, Ray, Peter, Meyn, Stephen, Cada, Michaela, Dror, Yigal

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Predictors of Disease Progression and Survival in Patients with Myelodysplastic Syndrome Secondary to Inherited Bone Marrow Failure Syndromes von Pabari, Reena, Cohen, Elisa, Cuvelier, Geoff D.E., Klaassen, Robert J., Villeneuve, Stephanie, Brossard, Josee, Abish, Sharon, Steele, MacGregor, Pastore, Yves D., Lipton, Jeffrey H., Rayar, Meera, Breakey, Vicky R., Wheaton, Laura, Jardine, Lawrence, Sinha, Roona, Goodyear, Lisa, Michon, Bruno, Corriveau-Bourque, Catherine, Sung, Lillian, Dror, Yigal, Cada, Michaela

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