Case 2: A pale infant – not a typical case of iron deficiency

par Wong, Michelle P, Wadsworth, Louis, Wu, John K, Dix, David
Publié 2008

Prevalence of Vitamin D Deficiency Varies Widely by Season in Canadian Children and Adolescents with Sickle Cell Disease

par Samson, Kaitlyn L. I., McCartney, Heather, Vercauteren, Suzanne M., Wu, John K., Karakochuk, Crystal D.
Publié dans J Clin Med (2018)

Utility of Anti-Xa Monitoring in Children Receiving Enoxaparin for Therapeutic Anticoagulation

par Leung, Marianna, Ho, Sharon H., Hamilton, Donald P., Wu, John K., Dix, David B., Wadsworth, Louis D., Ensom, Mary H. H.
Publié 2005

Folic acid supplementation in children with sickle cell disease: study protocol for a double-blind randomized cross-over trial

par Williams, Brock A., McCartney, Heather, Adams, Erin, Devlin, Angela M., Singer, Joel, Vercauteren, Suzanne, Wu, John K., Karakochuk, Crystal D.
Publié dans Trials (2020)

Detectable Unmetabolized Folic Acid and Elevated Folate Concentrations in Folic Acid-Supplemented Canadian Children With Sickle Cell Disease

par Williams, Brock A., Mayer, Cara, McCartney, Heather, Devlin, Angela M., Lamers, Yvonne, Vercauteren, Suzanne M., Wu, John K., Karakochuk, Crystal D.
Publié dans Front Nutr (2021)

Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy

par Lee, Jessica J. Y., van Karnebeek, Clara D. M., Drögemoller, Britt, Shyr, Casper, Tarailo-Graovac, Maja, Eydoux, Patrice, Ross, Colin J., Wasserman, Wyeth W., Björnson, Bruce, Wu, John K.
Publié dans Child Neurol Open (2016)

Hemophilia prophylaxis adherence and bleeding using a tailored, frequency‐escalated approach: The Canadian Hemophilia Primary Prophylaxis Study

par 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.
Publié dans Res Pract Thromb Haemost (2020)

The clinical impact of copy number variants in inherited bone marrow failure syndromes

par 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
Publié dans NPJ Genom Med (2017)

Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

par Sims, Matthew C., Mayer, Louisa, Collins, Janine H., Bariana, Tadbir K., Megy, Karyn, Lavenu-Bombled, Cecile, Seyres, Denis, Kollipara, Laxmikanth, Burden, Frances S., Greene, Daniel, Lee, Dave, Rodriguez-Romera, Antonio, Alessi, Marie-Christine, Astle, William J., Bahou, Wadie F., Bury, Loredana, Chalmers, Elizabeth, Da Silva, Rachael, De Candia, Erica, Deevi, Sri V. V., Farrow, Samantha, Gomez, Keith, Grassi, Luigi, Greinacher, Andreas, Gresele, Paolo, Hart, Dan, Hurtaud, Marie-Françoise, Kelly, Anne M., Kerr, Ron, Le Quellec, Sandra, Leblanc, Thierry, Leinøe, Eva B., Mapeta, Rutendo, McKinney, Harriet, Michelson, Alan D., Morais, Sara, Nugent, Diane, Papadia, Sofia, Park, Soo J., Pasi, John, Podda, Gian Marco, Poon, Man-Chiu, Reed, Rachel, Sekhar, Mallika, Shalev, Hanna, Sivapalaratnam, Suthesh, Steinberg-Shemer, Orna, Stephens, Jonathan C., Tait, Robert C., Turro, Ernest, Wu, John K. M., Zieger, Barbara, Kuijpers, Taco W., Whetton, Anthony D., Sickmann, Albert, Freson, Kathleen, Downes, Kate, Erber, Wendy N., Frontini, Mattia, Nurden, Paquita, Ouwehand, Willem H., Favier, Remi, Guerrero, Jose A.
Publié dans Blood (2020)