Publications by authors named "R Motyka"

: The risk of depression during pregnancy and postpartum is high and has intensified during the COVID-19 pandemic. The aim of this study was to estimate the risk of depressive disorders and self-harm thoughts in the third trimester of pregnancy and the first week postpartum in the pandemic period. : This study involved a total of 317 pregnant and postpartum women.

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Background: We aimed to develop a tool for predicting HNF1B mutations in children with congenital abnormalities of the kidneys and urinary tract (CAKUT).

Methods: The clinical and laboratory data from 234 children and young adults with known HNF1B mutation status were collected and analyzed retrospectively. All subjects were randomly divided into a training (70%) and a validation set (30%).

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Fullerenes have been long investigated for application as singlet oxygen sources. Even though they possess high photosensitizing efficiency, their practical use is still limited, mostly because of insufficient absorption of visible and/or near-infrared light. This limitation can be overcome by introducing organic chromophores that absorb longer-wavelength light, either by covalent attachment to C or by its encapsulation in a polymeric matrix.

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Within the presented work, we propose a complex photoemission-based approach for the investigation of the CThSe dyad (CThSe)/indium-tin oxide (ITO) interface formation. For surface topography and basic morphology determination, atomic force microscopy was utilized, and the results showed that CThSe agglomerated into close-to-spherical crystallites and the island-like growth was the dominant type for fullerene growth on the ITO substrate. Further, detailed X-ray and UV-photoelectron spectroscopies (XPS, UPS) were used for thorough characterization of the chemical and electronic properties of the investigated structures.

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Article Synopsis
  • - The study explores the relationship between hyperuricemia and nephropathy in children, specifically looking at those with and without mutations in the hepatocyte nuclear factor-1B gene.
  • - 108 pediatric patients were analyzed, revealing higher instances of hyperuricemia in those with the mutation, but no significant differences in other clinical characteristics between the two groups.
  • - While hyperuricemia is common in nephropathy, it is not a reliable predictor of genetic mutations due to its strong association with renal function, making it less useful as a diagnostic marker.
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