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

по Chan, Alicia K.J.
Опубликовано 2003

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

по Ferreira, Patrick, Chan, Alicia, Wolf, Barry
Опубликовано в: JIMD Rep (2017)

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

по Leung, Alexander A. C., Chan, Alicia K., Ezekowitz, Justin A., Leung, Alexander K. C.
Опубликовано 2009

Familial Recurrence of Cerebral Palsy with Multiple Risk Factors

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

Mitochondriome and Cholangiocellular Carcinoma

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

Cognitive Impairment In Treatment-Naïve Bipolar II and Unipolar Depression

по 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
Опубликовано в: 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...

по 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.
Опубликовано в: JIMD Rep (2020)

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

по 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.
Опубликовано в: Genet Med (2016)

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

по 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
Опубликовано в: 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...

по 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
Опубликовано в: Orphanet J Rare Dis (2020)