Publications by authors named "A A Sidorina"

Methylmalonic acidemia (MMA), propionic acidemia (PA), and cobalamin C deficiency (cblC) share a defect in propionic acid metabolism. In addition, cblC is also involved in the process of homocysteine remethylation. These three diseases produce various phenotypes and complex downstream metabolic effects.

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Article Synopsis
  • Liver and kidney transplantation in patients with methylmalonic aciduria shows potential for improving neurological outcomes, as assessed through clinical evaluations and biomarker measurements before and after the procedure.
  • Significant improvements were noted in primary and secondary biomarkers in plasma, while mitochondrial dysfunction markers decreased in cerebrospinal fluid (CSF), suggesting a positive shift in metabolic status post-transplant.
  • Neurocognitive assessments indicated improved developmental scores and brain health post-transplant, although some patients experienced reversible neurological issues that required differentiation to determine their cause; early transplantation is recommended due to the risks associated with long-term complications.
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Objective: Normal circadian rhythms are essential to the repair mechanisms of oxidative stress implicated in skin aging. Given reports that hyaluronic acid (HA) homeostasis exhibits a different profile in chronological skin aging, as compared to environmental or extrinsic aging, an improved understanding of the way HA interacts with its surroundings, and the impact of HA injectables in replacing lost HA and encouraging rejuvenation, is of key benefit to skin aging treatments. The objectives of these current studies were twofold.

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Introduction: Skin aging is a natural process that cannot be stopped. However, there are many ways to help attenuate premature aging of the skin and reduce the signs that have already appeared. One of them is the subcutaneous administration of preparations containing a combination of hyaluronic acid, active amino acids, and peptides providing an anti-aging clinical effect.

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Background: Ethylmalonic encephalopathy (EE) is a severe intoxication-type metabolic disorder with multisystem clinical features and leading to early death. In 2014, based on the promising results obtained by liver-targeted gene therapy in Ethe1 mouse model, we successfully attempted liver transplantation in a 9-month-old EE girl. Here we report her long-term follow-up, lasting over 6 years, with a comprehensive evaluation of clinical, instrumental and biochemical assessments.

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