Development of pharmacological strategies for mitochondrial disorders

per Kanabus, M, Heales, S J, Rahman, S
Publicat 2014

Persistent Mitochondrial Damage by Nitric Oxide and its Derivatives: Neuropathological Implications

per Bolaños, Juan P., Heales, Simon J. R.
Publicat 2010

Clinical Features and Pharmacotherapy of Childhood Monoamine Neurotransmitter Disorders

per Ng, J., Heales, S. J. R., Kurian, M. A.
Publicat 2014

Role of Intramuscular Levofolinate Administration in the Treatment of Hereditary Folate Malabsorption: Report of Three Cases

per Manea, Emanuela, Gissen, Paul, Pope, Simon, Heales, Simon J., Batzios, Spyros
Publicat a JIMD Rep (2017)

Tetrahydrobiopterin regulates cyclic GMP-dependent electrogenic Cl- secretion in mouse ileum in vitro.

per Rolfe, V E, Brand, M P, Heales, S J, Lindley, K J, Milla, P J
Publicat 1997

Investigation of changes in bone density and chemical composition associated with bone marrow oedema-type appearances in magnetic resonance images of the equine forelimb

per Heales, Christine J., Summers, Ian R., Fulford, Jonathan, Knapp, Karen M., Winlove, C. Peter
Publicat a BMC Musculoskelet Disord (2019)

Biochemical Diagnosis of Coenzyme Q(10) Deficiency

per Yubero, Delia, Montero, Raquel, Artuch, Rafael, Land, John M., Heales, Simon J.R., Hargreaves, Iain P.
Publicat 2014

Evidence for increased nitric oxide production in multiple sclerosis.

per Johnson, A W, Land, J M, Thompson, E J, Bolaños, J P, Clark, J B, Heales, S J
Publicat 1995

Incidence and characteristics of ventilator-associated pneumonia in a regional non-tertiary Australian intensive care unit: protocol for a retrospective clinical audit study

per Watson, Kirsty, Heales, Luke J, Fernando, Jeremy, Reoch, Josephine, Tan, Elise, Smith, Karen, Austin, David, Divanoglou, Anestis
Publicat a BMJ Open (2018)

Inhibition of Mitochondrial Complex I Impairs Release of α-Galactosidase by Jurkat Cells

per Lambert, Jonathan R. A., Howe, Steven J., Rahim, Ahad A., Burke, Derek G., Heales, Simon J. R.
Publicat a Int J Mol Sci (2019)

Can Sleep Be Used as an Indicator of Overreaching and Overtraining in Athletes?

per Lastella, Michele, Vincent, Grace E., Duffield, Rob, Roach, Gregory D., Halson, Shona L., Heales, Luke J., Sargent, Charli
Publicat a Front Physiol (2018)

Advances in methods to analyse cardiolipin and their clinical applications

per Bautista, Javier S., Falabella, Micol, Flannery, Padraig J., Hanna, Michael G., Heales, Simon J.R., Pope, Simon A.S., Pitceathly, Robert D.S.
Publicat a Trends Analyt Chem (2022)

Glucocerebrosidase Deficiency in Substantia Nigra of Parkinson Disease Brains

per Gegg, Matthew E, Burke, Derek, Heales, Simon J R, Cooper, J Mark, Hardy, John, Wood, Nicholas W, Schapira, Anthony H V
Publicat 2012

The pleiotropic effects of decanoic acid treatment on mitochondrial function in fibroblasts from patients with complex I deficient Leigh syndrome

per Kanabus, Marta, Fassone, Elisa, Hughes, Sean David, Bilooei, Sara Farahi, Rutherford, Tricia, Donnell, Maura O’, Heales, Simon J. R., Rahman, Shamima
Publicat a J Inherit Metab Dis (2016)

Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort

per Atkins, Janice L., Pilling, Luke C., Heales, Christine J., Savage, Sharon, Kuo, Chia-Ling, Kuchel, George A., Steffens, David C., Melzer, David
Publicat a J Alzheimers Dis (2021)

CoQ(10) Deficient Endothelial Cell Culture Model for the Investigation of CoQ(10) Blood–Brain Barrier Transport

per Wainwright, Luke, Hargreaves, Iain P., Georgian, Ana R., Turner, Charles, Dalton, R. Neil, Abbott, N. Joan, Heales, Simon J. R., Preston, Jane E.
Publicat a J Clin Med (2020)

Altered skeletal muscle insulin signaling and mitochondrial complex II-III linked activity in adult offspring of obese mice

per Shelley, Piran, Martin-Gronert, Malgorzata S., Rowlerson, Anthea, Poston, Lucilla, Heales, S. J. R., Hargreaves, Iain P., McConnell, Josie M., Ozanne, Susan E., Fernandez-Twinn, Denise S.
Publicat 2009

OP55 BIOCHEMICAL ANALYSIS COMBINED WITH 3D STRUCTURAL PROTEIN MODELLING IDENTIFIES THE ROLE OF SPECIFIC MITOCHONDRIAL MUTATIONS IN GBM

per Keatley, Kathleen, Polyzoidis, Stavros, Ashkan, Keyoumars, Heales, Simon J., Fillmore, Helen L., Hargreaves, Iain P., McGeehan, John E., Lloyd, Rhiannon E., Pilkington, Geoffrey J.
Publicat a Neuro Oncol (2015)

Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

per Bowron, Ann, Honeychurch, Julie, Williams, Maggie, Tsai-Goodman, Beverley, Clayton, Nicol, Jones, Lucy, Shortland, Graham J., Qureshi, Shakeel A., Heales, Simon J. R., Steward, Colin G.
Publicat a J Inherit Metab Dis (2014)

Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

per Bowron, Ann, Honeychurch, Julie, Williams, Maggie, Tsai-Goodman, Beverley, Clayton, Nicol, Jones, Lucy, Shortland, Graham J., Qureshi, Shakeel A., Heales, Simon J. R., Steward, Colin G.
Publicat a J Inherit Metab Dis (2015)