Page results
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The National Paediatric Diabetes Audit (NPDA) is asking all children and young people (8-19 years) and parents/carers (of children under 8 years old) who have received diabetes care in the past 6 months, to fill in the survey.
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The Clinical and Research Informatics Unit at UCLH consists of a team of clinicians, researchers, software developers, business intelligence analysts and data scientists working together to develop a robust environment for the analysis of clinical data.
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A front page story and patient case study highlight SUMMIT Study early diagnosis outcomes.
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Information for service users about the RESPOND service for refugees and asylum seekers.
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This page has been written for parents and carers whose child is having radiotherapy treatment to the whole brain and spine. This treatment may also be referred to as whole central nervous system (CNS) or cranio-spinal radiotherapy.
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This page has been written for parents and carers whose child is having total body irradiation (TBI) for leukaemia, lymphoma, or some other rare blood disorder.
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UCLH NHS Foundation Trust has once again formed a partnership with the Business Design Centre in Islington to reopen a large-scale COVID-19 vaccination centre on site from Saturday 18 December.
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This page is for patients with obesity who are waiting for scheduled surgery.
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University College London Hospitals (UCLH) is now administering new COVID-19 treatments for patients at highest risk in the community.
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Having proton beam therapy: information for children aged 5- 8 patient information leaflet
File results
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FOI201769 A&E attendances by patients with mental health related issues
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Charity Matters magazine - Winter 2020
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FOI201771 Cataract and glaucoma operations
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FOI201774 Maternity services
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FOI201776 Serious incidents and deaths of patients with a learning disability
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FOI/2023/0275 - Trust statistics on spiking
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FOI/2023/0262 - Clinical trial participation
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FOI/2023/0332 - Eating disorder services and Advance Decisions/ Directives to refuse medical treatment (ADRTs)
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FOI/2023/0260 - Treatment for rare diseases: Fabry, Gaucher and Pompe disease and Hunter Syndrome
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FOI/2023/0226 - Treatment with Nivolumab