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1.
Early Interv Psychiatry ; 16(12): 1345-1352, 2022 12.
Artículo en Inglés | MEDLINE | ID: mdl-35338593

RESUMEN

AIM: Clinical assessments are vital for gaining an understanding of a patients' presenting problem. A priority for Early Intervention in Psychosis Service staff is understanding and supporting their patients' experiences of hallucinations and/or delusions. We aimed to identify what cognitive-phenomenology dimensions of hallucinations and delusions EIPS staff were assessing with their patients. METHODS: We developed a brief checklist of cognitive-phenomenological dimensions of hallucinations and delusions called the Lived Experience Symptom Survey (LESS) based on relevant literature. As part of a Quality Improvement Project, we reviewed the health records of a sub-sample of EIPS patients using the LESS identifying whether each dimension was present or absent. RESULTS: We found that all patients had been asked about the content of their hallucinations and/or delusions, and the majority had been asked about the valence of this content. Despite patients having experienced psychosis for almost 2 years on average, less than half of patients were asked about the potential or actual harm associated with these symptoms. All other cognitive-phenomenological dimensions were assessed inconsistently. CONCLUSIONS: The assessment of hallucination and delusions in our EIPS was inconsistent and incomprehensive. These findings require replication in other EIPS' but may point to a need for guidelines and training around how to conduct a thorough assessment of hallucinations and delusions for current and future EIPS staff. Improved assessment of these symptoms will aid the development of risk assessments and treatment plans.


Asunto(s)
Deluciones , Trastornos Psicóticos , Humanos , Deluciones/diagnóstico , Deluciones/terapia , Mejoramiento de la Calidad , Trastornos Psicóticos/diagnóstico , Trastornos Psicóticos/complicaciones , Alucinaciones/diagnóstico , Alucinaciones/complicaciones , Cognición
2.
Dermatol Ther ; 22(6): 475-90, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19889133

RESUMEN

Filariasis is an infectious disease of the lymphatics and subcutaneous tissues caused by nematodes or filariae. Carried by mosquito vectors, this disease causes millions of people to suffer from lymphedema and elephantiasis, characteristics of filariasis infection. This disease can be diagnosed through the identification of microfilariae in blood or skin samples, antigen detection, radiographic imaging, or polymerase chain reaction. Mass drug administration by the World Health Organization has helped to diminish the incidence of filariasis. However, continued research on new drugs and vaccinations will be needed to control and reduce the microfilarial levels in the human population.


Asunto(s)
Antiparasitarios/uso terapéutico , Filariasis Linfática/diagnóstico , Filariasis Linfática/tratamiento farmacológico , Enfermedades Endémicas , Filariasis Linfática/epidemiología , Salud Global , Humanos , Incidencia
3.
Nat Commun ; 7: 10466, 2016 Jan 28.
Artículo en Inglés | MEDLINE | ID: mdl-26818444

RESUMEN

The Escherichia coli SMC complex, MukBEF, forms clusters of molecules that interact with the decatenase topisomerase IV and which are normally associated with the chromosome replication origin region (ori). Here we demonstrate an additional ATP-hydrolysis-dependent association of MukBEF with the replication termination region (ter). Consistent with this, MukBEF interacts with MatP, which binds matS sites in ter. MatP displaces wild-type MukBEF complexes from ter, thereby facilitating their association with ori, and limiting the availability of topoisomerase IV (TopoIV) at ter. Displacement of MukBEF is impaired when MukB ATP hydrolysis is compromised and when MatP is absent, leading to a stable association of ter and MukBEF. Impairing the TopoIV-MukBEF interaction delays sister ter segregation in cells lacking MatP. We propose that the interplay between MukBEF and MatP directs chromosome organization in relation to MukBEF clusters and associated topisomerase IV, thereby ensuring timely chromosome unlinking and segregation.


Asunto(s)
Proteínas Cromosómicas no Histona/metabolismo , Segregación Cromosómica , Topoisomerasa de ADN IV/metabolismo , Proteínas de Escherichia coli/metabolismo , Escherichia coli/genética , Proteínas Represoras/metabolismo , División Celular , Proteínas Cromosómicas no Histona/genética , Cromosomas Bacterianos/genética , Cromosomas Bacterianos/metabolismo , Topoisomerasa de ADN IV/genética , ADN Bacteriano/genética , Escherichia coli/metabolismo , Proteínas de Escherichia coli/genética , Origen de Réplica , Proteínas Represoras/genética
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