Publications by authors named "E Odell"

Article Synopsis
  • Preterm white matter injury (PWMI) is a primary cause of brain injury in premature infants, and clemastine has shown promise in promoting myelination in affected mouse models at a dose of 10 mg/kg/day.* -
  • This study aimed to determine the minimum effective dose (MED) of clemastine in neonatal mice, hypothesizing it to be lower than 10 mg/kg/day; they found the MED to be 7.5 mg/kg/day for rescuing hypoxia-induced hypomyelination.* -
  • The results highlight the potential for clemastine as a treatment for PWMI, providing essential data on dosing and pharmacokinetics that will aid future clinical trials in neonates
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Adenoid ameloblastoma (AA) was recently recognised as a separate tumour type in the most recent World Health Organisation (WHO) classification of head and neck tumours. This decision has been considered controversial by several groups, who have described AA as a subtype of ameloblastoma, a hybrid odontogenic tumour or to fall within the spectrum of other recognised odontogenic tumours, including dentinogenic ghost cell tumour and adenomatoid odontogenic tumour. Here we review the reasons for the WHO decision to classify AA as a separate tumour type.

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Background: Preterm white matter injury (PWMI) is the most common cause of brain injury in premature neonates. PWMI involves a differentiation arrest of oligodendrocytes, the myelinating cells of the central nervous system. Clemastine was previously shown to induce oligodendrocyte differentiation and myelination in mouse models of PWMI at a dose of 10 mg/kg/day.

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Objectives: The incidence of head and neck squamous cell carcinoma (HNSCC) continues to increase and although advances have been made in treatment, it still has a poor overall survival with local relapse being common. Conventional imaging methods are not efficient at detecting recurrence at an early stage when still potentially curable. The aim of this study was to test the feasibility of using saliva to detect the presence of oral squamous cell carcinoma (OSCC) and to provide additional evidence for the potential of this approach.

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