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Kees Brinkman

Researcher at Henry Ford Hospital

Publications -  134
Citations -  6945

Kees Brinkman is an academic researcher from Henry Ford Hospital. The author has contributed to research in topics: Lamivudine & Men who have sex with men. The author has an hindex of 40, co-authored 120 publications receiving 6289 citations.

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Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway.

TL;DR: Although the introduction of protease inhibitors has changed management of HIV infection drastically, this cerebro-protective property will assert the role of these nucleo-side RT inhibitors (NRTI) as a cornerstone ofantiretroviral therapy.
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Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophy

TL;DR: It is postulate that the mitochondrial toxicity of the nucleoside-analogue reverse-transcriptase inhibitors plays an essential part in the development of this lipodystrophy, similar to the role of mitochondrial defects in theDevelopment of multiple symmetrical lipomatosis.
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Future challenges for clinical care of an ageing population infected with HIV: a modelling study

TL;DR: The profile of patients in the Netherlands infected with HIV is changing, with increasing numbers of older patients with multiple morbidities, which means that, in the near future, HIV care will increasingly need to draw on a wide range of medical disciplines, in addition to evidence-based screening and monitoring protocols to ensure continued high-quality care.
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Life expectancy of recently diagnosed asymptomatic HIV-infected patients approaches that of uninfected individuals

TL;DR: The life expectancy of asymptomatic HIV-infected patients who are still treatment-naive and have not experienced a CDC-B or C event at 24 weeks after diagnosis approaches that of non- Infected individuals, however, follow-up time is short compared to the expected number of years lived.
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Mortality and progression to AIDS after starting highly active antiretroviral therapy.

TL;DR: Survival probabilities were high among HIV-infected patients initiating HAART at an early stage of infection, and the best therapy strategy is therefore to startHAART at this stage of infections, however, deferring HAART in patients with high CD4 cell counts may be clinically more appropriate given toxicity and adherence problems.