The University of Queensland

Diet, disease severity, and energy expenditure in amyotrophic lateral sclerosis (ALS)

Castles, Zoe, Buckett, Lauren, Jiang, Leanne, Steyn, Frederik J. and Ngo, Shyuan T. (2023). Diet, disease severity, and energy expenditure in amyotrophic lateral sclerosis (ALS). Diet and nutrition in neurological disorders. (pp. 123-140) edited by Colin R. Martin, Vinood B. Patel and Victor R. Preedy. Amsterdam, Netherlands: Elsevier. doi: 10.1016/b978-0-323-89834-8.00007-6

Generation of human induced pluripotent stem cell lines from sporadic, sporadic frontotemporal dementia, familial SOD1, and familial C9orf72 amyotrophic lateral sclerosis (ALS) patients

Jiang, Leanne, Tracey, Timothy J., Gill, Melinder K., Howe, Stephanie L., Power, Dominique T., Bharti, Vanda, McCombe, Pamela A., Henderson, Robert D., Steyn, Frederik J. and Ngo, Shyuan T. (2024). Generation of human induced pluripotent stem cell lines from sporadic, sporadic frontotemporal dementia, familial SOD1, and familial C9orf72 amyotrophic lateral sclerosis (ALS) patients. Stem Cell Research, 78 103447, 103447. doi: 10.1016/j.scr.2024.103447

Generation of a human induced pluripotent stem cell line (UQi001-A-1) edited with the CRISPR-Cas9 system to carry the heterozygous TARDBP c.1144G>A (p.A382T) missense mutation

Tracey, Timothy J., Jiang, Leanne, Gill, Melinder K., Ranie, Samara N., Ovchinnikov, Dmitry A., Wolvetang, Ernst J. and Ngo, Shyuan T. (2023). Generation of a human induced pluripotent stem cell line (UQi001-A-1) edited with the CRISPR-Cas9 system to carry the heterozygous TARDBP c.1144G>A (p.A382T) missense mutation. Stem Cell Research, 70 103137, 1-6. doi: 10.1016/j.scr.2023.103137

ALSUntangled #65: glucocorticoid corticosteroids

Goslinga, Jill Ann, Terrelonge, Mark, Bedlack, Richard, Barkhaus, Paul, Barnes, Benjamin, Bertorini, Tulio, Bromberg, Mark, Carter, Gregory, Chen, Amy, Crayle, Jesse, Dimachkie, Mazen, Jiang, Leanne, Levitsky, Gleb, Lund, Isaac, Martin, Sarah, Mcdermott, Christopher, Pattee, Gary, Pierce, Kaitlyn, Ratner, Dylan, Slachtova, Lenka, Sun, Yuyao and Wicks, Paul (2022). ALSUntangled #65: glucocorticoid corticosteroids. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 24 (3-4), 1-7. doi: 10.1080/21678421.2022.2099746

Altered TDP-43 structure and function: key insights into aberrant RNA, mitochondrial, and cellular and systemic metabolism in amyotrophic lateral sclerosis

Jiang, Leanne and Ngo, Shyuan T. (2022). Altered TDP-43 structure and function: key insights into aberrant RNA, mitochondrial, and cellular and systemic metabolism in amyotrophic lateral sclerosis. Metabolites, 12 (8) 709, 1-29. doi: 10.3390/metabo12080709

Evaluation of an Australian neurological nurse-led model of postdischarge care

Pugh, Judith Dianne, McCoy, Kathleen, Needham, Merrilee, Jiang, Leanne, Giles, Margaret, McKinnon, Elizabeth and Heine, Kym (2022). Evaluation of an Australian neurological nurse-led model of postdischarge care. Health and Social Care in the Community, 30 (4), E962-E973. doi: 10.1111/hsc.13498

Winners and losers in palliative care service delivery: Time for a public health approach to palliative and end of life care

Aoun, Samar M., Richmond, Robyn, Jiang, Leanne and Rumbold, Bruce (2021). Winners and losers in palliative care service delivery: Time for a public health approach to palliative and end of life care. Healthcare, 9 (12), 1615. doi: 10.3390/healthcare9121615

Why and how the work of Motor Neurone Disease Associations matters before and during bereavement: a consumer perspective

Aoun, Samar M., Cafarella, Paul A., Hogden, Anne, Thomas, Geoff, Jiang, Leanne and Edis, Robert (2021). Why and how the work of Motor Neurone Disease Associations matters before and during bereavement: a consumer perspective. Palliative Care and Social Practice, 15 ARTN 26323524211009537, 263235242110095. doi: 10.1177/26323524211009537

Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease

Aoun, Samar M., Cafarella, Paul A., Rumbold, Bruce, Thomas, Geoff, Hogden, Anne, Jiang, Leanne, Gregory, Sonia and Kissane, David W. (2021). Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22 (1-2), 12-22. doi: 10.1080/21678421.2020.1813780

ALSUntangled 58: Azathioprine

Bedlack, Richard, Armon, Carmel, Barkhaus, Paul, Bertorini, Tulio, Bowser, Robert, Carter, Greg, Crayle, Jesse, Jiang, Leanne, Levitsky, Gleb, McDermott, Christopher, Paganoni, Sabrina, Pattee, Gary, Salmon, Kristiana, Stephens, James and Wicks, Paul (2020). ALSUntangled 58: Azathioprine. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22 (7-8), 592-594. doi: 10.1080/21678421.2020.1809821

Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study

Aoun, Samar M., Kissane, David W., Cafarella, Paul A., Rumbold, Bruce, Hogden, Anne, Jiang, Leanne and Bear, Natasha (2020). Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 21 (7-8), 593-605. doi: 10.1080/21678421.2020.1790610

Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis

Pytte, Julia, Anderton, Ryan S., Flynn, Loren, Theunissen, Frances, Jiang, Leanne, Pitout, Ianthe, James, Ian, Mastaglia, Frank L., Saunders, Ann M., Bedlack, Richard, Siddique, Teepu, Siddique, Nailah and Akkari, P. Anthony (2020). Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis. Neurology: Genetics, 6 (2), e406. doi: 10.1212/nxg.0000000000000406

Structural variants may be a source of missing heritability in sALS

Theunissen, Frances, Flynn, Loren L., Anderton, Ryan S., Mastaglia, Frank, Pytte, Julia, Jiang, Leanne, Hodgetts, Stuart, Burns, Daniel K., Saunders, Ann, Fletcher, Sue, Wilton, Steve D. and Akkari, Patrick Anthony (2020). Structural variants may be a source of missing heritability in sALS. Frontiers in Neuroscience, 14. doi: 10.3389/fnins.2020.00047