A comparison of current serum biomarkers as diagnostic indicators of mitochondrial diseases

por Davis, Ryan L., Liang, Christina, Sue, Carolyn M.
Publicado 2016

Outcome of patient with myasthenia gravis with the use of immunotherapy in metastatic Merkel cell carcinoma

por Williams, Sarah, Liang, Christina, Guminski, Alexander, Hruby, George, Chan, David
Publicado 2022

Applying landscape genomic tools to forest management and restoration of Hawaiian koa (Acacia koa) in a changing environment

por Gugger, Paul F., Liang, Christina T., Sork, Victoria L., Hodgskiss, Paul, Wright, Jessica W.
Publicado 2017

Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zone

por Bryen, Samantha J., Yuen, Michaela, Joshi, Himanshu, Dawes, Ruebena, Zhang, Katharine, Lu, Jessica K., Jones, Kristi J., Liang, Christina, Wong, Wui-Kwan, Peduto, Anthony J., Waddell, Leigh B., Evesson, Frances J., Cooper, Sandra T.
Publicado 2022

Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis

por Davis, Ryan L., Kumar, Kishore R., Puttick, Clare, Liang, Christina, Ahmad, Kate E., Edema-Hildebrand, Fabienne, Park, Jin-Sung, Minoche, Andre E., Gayevskiy, Velimir, Mallawaarachchi, Amali C., Christodoulou, John, Schofield, Deborah, Dinger, Marcel E., Cowley, Mark J., Sue, Carolyn M.
Publicado 2022

Rehabilitation for ataxia study: protocol for a randomised controlled trial of an outpatient and supported home-based physiotherapy programme for people with hereditary cerebellar...

por Milne, Sarah C, Corben, Louise A, Roberts, Melissa, Szmulewicz, David, Burns, J, Grobler, Anneke C, Williams, Shannon, Chua, Jillian, Liang, Christina, Lamont, Phillipa J, Grootendorst, Alison C, Massey, Libby, Sue, Carolyn, Dalziel, Kim, LaGrappe, Desiree, Willis, Liz, Freijah, Aleka, Gerken, Paul, Delatycki, Martin B
Publicado 2020

Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations

por Sue, Carolyn M., Balasubramaniam, Shanti, Bratkovic, Drago, Bonifant, Catherine, Christodoulou, John, Coman, David, Crawley, Karen, Edema‐Hildebrand, Fabienne, Ellaway, Carolyn, Ghaoui, Roula, Kava, Maina, Kearns, Lisa S., Lee, Joy, Liang, Christina, Mackey, David A., Murray, Sean, Needham, Merrilee, Rius, Rocio, Russell, Jacqui, Smith, Nicholas J.C., Thyagarajan, Dominic, Wools, Christine
Publicado 2021

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis

por Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M., Brady, Stefen, Holton, Janice L., Pittman, Alan M., Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David, Shieh, Perry B., Needham, Merrilee, Liang, Christina, Zanoteli, Edmar, de Camargo, Leonardo Valente, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J., Dimachkie, Mazen M., Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Singleton, Andrew B., Hanna, Michael G., Houlden, Henry
Publicado 2016