Development of pharmacological strategies for mitochondrial disorders

por Kanabus, M, Heales, S J, Rahman, S
Publicado em 2014

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

por Bolaños, Juan P., Heales, Simon J. R.
Publicado em 2010

Clinical Features and Pharmacotherapy of Childhood Monoamine Neurotransmitter Disorders

por Ng, J., Heales, S. J. R., Kurian, M. A.
Publicado em 2014

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

por Manea, Emanuela, Gissen, Paul, Pope, Simon, Heales, Simon J., Batzios, Spyros
Publicado no JIMD Rep (2017)

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

por Rolfe, V E, Brand, M P, Heales, S J, Lindley, K J, Milla, P J
Publicado em 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

por Heales, Christine J., Summers, Ian R., Fulford, Jonathan, Knapp, Karen M., Winlove, C. Peter
Publicado no BMC Musculoskelet Disord (2019)

Biochemical Diagnosis of Coenzyme Q(10) Deficiency

por Yubero, Delia, Montero, Raquel, Artuch, Rafael, Land, John M., Heales, Simon J.R., Hargreaves, Iain P.
Publicado em 2014

Evidence for increased nitric oxide production in multiple sclerosis.

por Johnson, A W, Land, J M, Thompson, E J, Bolaños, J P, Clark, J B, Heales, S J
Publicado em 1995

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

por Watson, Kirsty, Heales, Luke J, Fernando, Jeremy, Reoch, Josephine, Tan, Elise, Smith, Karen, Austin, David, Divanoglou, Anestis
Publicado no BMJ Open (2018)

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

por Lambert, Jonathan R. A., Howe, Steven J., Rahim, Ahad A., Burke, Derek G., Heales, Simon J. R.
Publicado no Int J Mol Sci (2019)

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

por Lastella, Michele, Vincent, Grace E., Duffield, Rob, Roach, Gregory D., Halson, Shona L., Heales, Luke J., Sargent, Charli
Publicado no Front Physiol (2018)

Advances in methods to analyse cardiolipin and their clinical applications

por Bautista, Javier S., Falabella, Micol, Flannery, Padraig J., Hanna, Michael G., Heales, Simon J.R., Pope, Simon A.S., Pitceathly, Robert D.S.
Publicado no Trends Analyt Chem (2022)

Glucocerebrosidase Deficiency in Substantia Nigra of Parkinson Disease Brains

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

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

por Kanabus, Marta, Fassone, Elisa, Hughes, Sean David, Bilooei, Sara Farahi, Rutherford, Tricia, Donnell, Maura O’, Heales, Simon J. R., Rahman, Shamima
Publicado no J Inherit Metab Dis (2016)

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

por Atkins, Janice L., Pilling, Luke C., Heales, Christine J., Savage, Sharon, Kuo, Chia-Ling, Kuchel, George A., Steffens, David C., Melzer, David
Publicado no J Alzheimers Dis (2021)

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

por Wainwright, Luke, Hargreaves, Iain P., Georgian, Ana R., Turner, Charles, Dalton, R. Neil, Abbott, N. Joan, Heales, Simon J. R., Preston, Jane E.
Publicado no J Clin Med (2020)

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

por 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.
Publicado em 2009

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

por Keatley, Kathleen, Polyzoidis, Stavros, Ashkan, Keyoumars, Heales, Simon J., Fillmore, Helen L., Hargreaves, Iain P., McGeehan, John E., Lloyd, Rhiannon E., Pilkington, Geoffrey J.
Publicado no Neuro Oncol (2015)

Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

por 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.
Publicado no J Inherit Metab Dis (2014)

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

por 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.
Publicado no J Inherit Metab Dis (2015)