Publications by authors named "Julia Braga"

Background: Intracranial teratomas represent a rare subset of neoplasms characterized by tissues derived from multiple germ layers within the cranial cavity. These tumors, originating from primordial germ cells, exhibit diverse clinical presentations and histopathological features. While predominantly located along the midline axis, including the suprasellar cistern and pineal region, they can also manifest in less common areas such as ventricles and hypothalamic regions.

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Article Synopsis
  • - The study aimed to investigate endoscopic and histopathological changes in the esophagus, stomach, and duodenum of Crohn's disease patients through esophagogastroduodenoscopies and biopsies, assessing bacterial presence with Giemsa staining.
  • - Out of 58 patients, significant findings included erosive esophagitis in 43.1%, gastritis in 55.2%, and erosive duodenitis in 13.8%, with varying inflammatory activity noted in patients with and without bacterial infection.
  • - The findings revealed a prevalence of nonspecific changes linked to Crohn's disease, with rare instances of focally enhanced gastritis, while factors like time since diagnosis, age, and ongoing treatments
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Aim: To assess the influence of co-culture with mineral trioxide aggregate (MTA) and MTA Fillapex (FLPX) on the viability, adherence, and phagocytosis activity of peritoneal macrophages from two mouse strains.

Methodology: Cellular viability, adherence, and phagocytosis of Saccharomyces boulardii were assayed in the presence of capillaries containing MTA and MTA Fillapex. The data were analyzed using parametric (Student's t) and non-parametric (Mann-Whitney) tests.

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The aim of this article is to describe the care of a patient with fibrodysplasia ossificans progressiva (FOP) and to provide dentists with a guide for how to safely care for patients with FOP. Treatment improved the patient's limited mouth opening. FOP is a rare autosomal dominant disorder characterized by congenital malformation of the fingers and toes by heterotopic ossification progressiva of the connective tissue.

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In Alzheimer's disease increasing evidence attributes synaptic and cognitive deficits to soluble oligomers of amyloid beta protein (Abeta), even prior to the accumulation of amyloid plaques, neurofibrillary tangles, and neuronal cell death. Here we show that within 1-2 h picomolar concentrations of cell-derived, soluble Abeta induce specific alterations in pre- and postsynaptic morphology and connectivity in cultured hippocampal neurons. Clusters of presynaptic vesicle markers decreased in size and number at glutamatergic but not GABAergic terminals.

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