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Salvatore Pepe

Researcher at Royal Children's Hospital

Publications -  131
Citations -  10554

Salvatore Pepe is an academic researcher from Royal Children's Hospital. The author has contributed to research in topics: Mitochondrion & Oxidative stress. The author has an hindex of 39, co-authored 128 publications receiving 9804 citations. Previous affiliations of Salvatore Pepe include University of Adelaide & Alfred Hospital.

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The Clinical Application of Metabolic Therapy for Cardiovascular Disease

TL;DR: Metabolic therapy involves the administration of a substance normally found in the body to enhance a metabolic reaction within the cell as mentioned in this paper, which may be achieved in two ways: first, for some systems a substance can be given to achieve greater than normal levels in the human body so as to drive an enzymic reaction in a preferred direction.
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Mitochondrial dysfunction in CD4 + lymphocytes from stavudine-treated HIV patients

TL;DR: Therapy with stavudine results in impaired mitochondrial function in CD4+PBLs that does not appear to be due to reduced mitochondrial volume or DNA content and cannot be attributed to infection with HIV.
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p38 Mitogen-Activated Protein Kinase Inhibition Reduces Inflammatory Cytokines in a Brain-Dead Transplant Donor Animal Model

TL;DR: In this paper, a small molecule inhibitor of p38 mitogen-activated protein kinase (p38 MAPK) was used in rat heart and lungs after experimentally induced brain death.
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Protective role of coenzyme Q10 in two models of rat lung injury.

TL;DR: The impact of Coenzyme Q10 pretreatment in a model of mild and severe lung injury is studied to study the protective effect in the lung of this potent antioxidant and cellular energizer.
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Skeletal myopathy associated with nucleoside reverse transcriptase inhibitor therapy: potential benefit of coenzyme Q10 therapy:

TL;DR: A 52-year-old man, who in 1985 developed ragged-red fibre myopathy 14 years after diagnosis of HIV infection while on effective ZDV-based combination antiretroviral therapy (ART), was treated with the mitochondrial anti-oxidant coenzyme Q10 and made an excellent recovery, potentially allowing continuation of antiviral treatments including ZdV.