854 research outputs found

    Alumni-onderzoek 2011

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    Puls, J (2011), Van den Munckhof, R (2011). Alumni-onderzoek 2011, The Netherlands: Instellingsbreed Platform Onderwijs (IPO).In dit rapport wordt een onderzoek gedaan onder Allumi. Bij deze groep is het interessant om na te gaan wat zij van onze opleidingen vinden, wat het effect is van hun studie op hun verdere leven en loopbaan. In hoeverre kunnen wij als de Open universiteit gebruik maken van hun ervaring, kennis en kunde? interessante vragen met even zo vele interessante antwoorden.

    The role of the homeobox transcription factor Pitx3 in the mesencephalic dopaminergic system

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    Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal

    Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains

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    Intestinal carriage of extended-spectrum beta-lactamase (ESBL) -producing bacteria in food-producing animals and contamination of retail meat may contribute to increased incidences of infections with ESBL-producing bacteria in humans. Therefore, distribution of ESBL genes, plasmids and strain genotypes in Escherichia coli obtained from poultry and retail chicken meat in the Netherlands was determined and defined as ‘poultry-associated’ (PA). Subsequently, the proportion of E. coli isolates with PA ESBL genes, plasmids and strains was quantified in a representative sample of clinical isolates. The E. coli were derived from 98 retail chicken meat samples, a prevalence survey among poultry, and 516 human clinical samples from 31 laboratories collected during a 3-month period in 2009. Isolates were analysed using an ESBL-specific microarray, sequencing of ESBL genes, PCR-based replicon typing of plasmids, plasmid multi-locus sequence typing (pMLST) and strain genotyping (MLST). Six ESBL genes were defined as PA (blaCTX-M-1, blaCTX-M-2, blaSHV-2, blaSHV-12, blaTEM-20, blaTEM-52): 35% of the human isolates contained PA ESBL genes and 19% contained PA ESBL genes located on IncI1 plasmids that were genetically indistinguishable from those obtained from poultry (meat). Of these ESBL genes, 86% were blaCTX-M-1 and blaTEM-52 genes, which were also the predominant genes in poultry (78%) and retail chicken meat (75%). Of the retail meat samples, 94% contained ESBL-producing isolates of which 39% belonged to E. coli genotypes also present in human samples. These findings are suggestive for transmission of ESBL genes, plasmids and E. coli isolates from poultry to humans, most likely through the food chain

    DSM-5-TR prolonged grief disorder and DSM-5 posttraumatic stress disorder are related, yet distinct:confirmatory factor analyses in traumatically bereaved people

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    Background: Prolonged grief disorder (PGD) is newly included in the text revision of the DSM-5 (DSM-5-TR). So far, it is unknown if DSM-5-TR PGD is distinguishable from bereavement-related posttraumatic stress disorder (PTSD). Prior research examining the distinctiveness of PTSD and pathological grief focused on non-traumatic loss samples, used outdated conceptualizations of grief disorders, and has provided mixed results. Objective: In a large sample of traumatically bereaved people, we first evaluated the factor structure of PTSD and PGD separately and then evaluated the factor structure when combining PTSD and PGD symptoms to examine the distinctiveness between the two syndromes. Methods: Self-reported data were used from 468 people bereaved due to the MH17 plane disaster (N = 200) or a traffic accident (N = 268). The 10 DSM-5-TR PGD symptoms were assessed with the Traumatic Grief Inventory-Self Report Plus (TGI-SR+). The 20-item Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) was used to tap PTSD symptoms. Confirmatory factor analyses were conducted. Results: For PTSD, a seven factor, so-called ‘Hybrid’ model yielded the best fit. For PGD, a univariate factor model fits the data well. A combined model with PGD items loading on one factor and PTSD items on seven factors (associations between PGD and PTSD subscales r ≥ .50 and ≤.71), plus a higher-order factor (i.e. PTSD factors on a higher-order PTSD factor) (association between higher-order PTSD factor and PGD factor r = .82) exhibited a better fit than a model with all PGD and PTSD symptom loading on a single factor or two factors (i.e. one for PGD and one for PTSD). Conclusions: This is the first study examining the factor structure of DSM-5-TR PGD and DSM-5 PTSD in people confronted with a traumatic loss. The findings provide support that PGD constitutes a syndrome distinguishable from, yet related with, PTSD

    Studentinzicht 11

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    Het laatste kwartaal van 2012 heeft opnieuw een peiling plaatsgevonden van Studentinzicht. De elfde alweer. In deze peiling zijn weer alle groepen meegenomen, dat wil zeggen: belangstellenden, recente inschrijvers, ervaren studenten en de groep uitstromers. Naast de bekende thema’s als informatievoorziening, begeleiding, binding e.d. zijn ditmaal ook vragen opgenomen met betrekking tot OUX. Wat vinden belangstellenden en studenten van een meer gestructureerd traject als OUX, welke voor- en nadelen zien zij? Daarnaast is aan de respondenten gevraagd een rapportcijfer te geven voor de Open Universiteit. We krijgen als instelling van alle groepen een ruime voldoende (7+), waarbij opleidingsstudenten hogere cijfers geven, vergeleken met de groep cursisten. Anders dan in voorgaande rapporten zijn de conclusies en aanbevelingen ditmaal niet in het rapport zelf opgenomen, maar bijgevoegd in een begeleidend schrijven. Deze aanbevelingen cq actiepunten zullen o.a. besproken worden binnen de CDHD (College van decanen en hoogleraar-directeuren)

    Deep brain stimulation of the central thalamus restores arousal and motivation in a zolpidem-responsive patient with akinetic mutism after severe brain injury

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    After severe brain injury, zolpidem is known to cause spectacular, often short-lived, restorations of brain functions in a small subgroup of patients. Previously, we showed that these zolpidem-induced neurological recoveries can be paralleled by significant changes in functional connectivity throughout the brain. Deep brain stimulation (DBS) is a neurosurgical intervention known to modulate functional connectivity in a wide variety of neurological disorders. In this study, we used DBS to restore arousal and motivation in a zolpidem-responsive patient with severe brain injury and a concomitant disorder of diminished motivation, more than 10 years after surviving hypoxic ischemia. We found that DBS of the central thalamus, targeted at the centromedian-parafascicular complex, immediately restored arousal and was able to transition the patient from a state of deep sleep to full wakefulness. Moreover, DBS was associated with temporary restoration of communication and ability to walk and eat in an otherwise wheelchair-bound and mute patient. With the use of magnetoencephalography (MEG), we revealed that DBS was generally associated with a marked decrease in aberrantly high levels of functional connectivity throughout the brain, mimicking the effects of zolpidem. These results imply that 'pathological hyperconnectivity' after severe brain injury can be associated with reduced arousal and behavioral performance and that DBS is able to modulate connectivity towards a 'healthier baseline' with lower synchronization, and, can restore functional brain networks long after severe brain injury. The presence of hyperconnectivity after brain injury may be a possible future marker for a patient's responsiveness for restorative interventions, such as DBS, and suggests that lower degrees of overall brain synchronization may be conducive to cognition and behavioral responsiveness
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