A clinical guide to inherited metabolic diseases, 2nd ed.

por Chan, Alicia K.J.
Publicado 2003

Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase Deficiency

por Ferreira, Patrick, Chan, Alicia, Wolf, Barry
Publicado en JIMD Rep (2017)

A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency

por Leung, Alexander A. C., Chan, Alicia K., Ezekowitz, Justin A., Leung, Alexander K. C.
Publicado 2009

Familial Recurrence of Cerebral Palsy with Multiple Risk Factors

por Richer, Lawrence P., Dower, Nancy A., Leonard, Norma, Chan, Alicia K. J., Robertson, Charlene M. T.
Publicado 2011

Mitochondriome and Cholangiocellular Carcinoma

por Bahitham, Wesam, Liao, Xiaoping, Peng, Fred, Bamforth, Fiona, Chan, Alicia, Mason, Andrew, Stone, Bradley, Stothard, Paul, Sergi, Consolato
Publicado 2014

Cognitive Impairment In Treatment-Naïve Bipolar II and Unipolar Depression

por Mak, Arthur D. P., Lau, Domily T. Y., Chan, Alicia K. W., So, Suzanne H. W., Leung, Owen, Wong, Sheila L. Y., Lam, Linda, Leung, C. M., Lee, Sing
Publicado en Sci Rep (2018)

Pre‐school neurocognitive and functional outcomes after liver transplant in children with early onset urea cycle disorders, maple syrup urine disease, and propionic acidemia: An in...

por Jain‐Ghai, Shailly, Joffe, Ari R., Bond, Gwen Y., Siriwardena, Komudi, Chan, Alicia, Yap, Jason Y. K., Hajihosseini, Morteza, Dinu, Irina A., Acton, Bryan V., Robertson, Charlene M. T.
Publicado en JIMD Rep (2020)

Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infants

por Jones, Simon A., Valayannopoulos, Vassili, Schneider, Eugene, Eckert, Stephen, Banikazemi, Maryam, Bialer, Martin, Cederbaum, Stephen, Chan, Alicia, Dhawan, Anil, Di Rocco, Maja, Domm, Jennifer, Enns, Gregory M., Finegold, David, Gargus, J. Jay, Guardamagna, Ornella, Hendriksz, Christian, Mahmoud, Iman G., Raiman, Julian, Selim, Laila A., Whitley, Chester B., Zaki, Osama, Quinn, Anthony G.
Publicado en Genet Med (2016)

Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada

por Lamoureux, Monica F., Tingley, Kylie, Kronick, Jonathan B., Potter, Beth K., Chan, Alicia K. J., Coyle, Doug, Dodds, Linda, Dyack, Sarah, Feigenbaum, Annette, Geraghty, Michael, Gillis, Jane, Rockman-Greenberg, Cheryl, Khan, Aneal, Little, Julian, MacKenzie, Jennifer, Maranda, Bruno, Mhanni, Aizeddin, Mitchell, John J., Mitchell, Grant, Laberge, Anne-Marie, Potter, Murray, Prasad, Chitra, Siriwardena, Komudi, Speechley, Kathy N., Stockler, Sylvia, Trakadis, Yannis, Turner, Lesley, Van Karnebeek, Clara, Wilson, Kumanan, Chakraborty, Pranesh
Publicado en JIMD Rep (2015)

Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Me...

por Tingley, Kylie, Lamoureux, Monica, Pugliese, Michael, Geraghty, Michael T., Kronick, Jonathan B., Potter, Beth K., Coyle, Doug, Wilson, Kumanan, Kowalski, Michael, Austin, Valerie, Brunel-Guitton, Catherine, Buhas, Daniela, Chan, Alicia K. J., Dyack, Sarah, Feigenbaum, Annette, Giezen, Alette, Goobie, Sharan, Greenberg, Cheryl R., Ghai, Shailly Jain, Inbar-Feigenberg, Michal, Karp, Natalya, Kozenko, Mariya, Langley, Erica, Lines, Matthew, Little, Julian, MacKenzie, Jennifer, Maranda, Bruno, Mercimek-Andrews, Saadet, Mohan, Connie, Mhanni, Aizeddin, Mitchell, Grant, Mitchell, John J., Nagy, Laura, Napier, Melanie, Pender, Amy, Potter, Murray, Prasad, Chitra, Ratko, Suzanne, Salvarinova, Ramona, Schulze, Andreas, Siriwardena, Komudi, Sondheimer, Neal, Sparkes, Rebecca, Stockler-Ipsiroglu, Sylvia, Trakadis, Yannis, Turner, Lesley, Van Karnebeek, Clara, Vallance, Hilary, Vandersteen, Anthony, Walia, Jagdeep, Wilson, Ashley, Wilson, Brenda J., Yu, Andrea C., Yuskiv, Nataliya, Chakraborty, Pranesh
Publicado en Orphanet J Rare Dis (2020)