Page results
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The Ataxia Centre brings together a team of specialists, with expertise in the diagnosis, management and research of all forms of ataxia.
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We offer comprehensive assessment, diagnostic services and investigation for all forms of the disease including neuropsychology, neurophysiology, imaging, genetic testing, and tissue diagnosis.
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You can make a secure payment using our online portal. It is a convenient way to make a payment for a range of services and is available 24/7. When making a payment you will be directed a secure website hosted by The Access Group, a leading provider of business software. Payments can be made against an invoice raised by the Trust or for a range of other services which are set out when you access the portal.
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The department specialises in the assessment and management of Complex Neuropsychiatric conditions occurring in the context of neurological disease.
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Skeletal muscle channelopathies are rare neuromuscular diseases that cause symptoms of episodic muscle weakness/paralysis or cause difficulty in relaxing muscles (the muscle can feel stuck or cramped) once they are contracted.
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This page is for patients who are about to start a course of radiotherapy to the prostate/prostate bed.
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This booklet is designed for teenagers and young people. It explains what you can expect when you finish your treatment for Hodgkin lymphoma.
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Information and advice for patients, relatives and carers about thoracic surgery.
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The maternity team at UCLH will listen to your hopes and concerns and can suggest helpful and practical ideas to help you.
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The service offers psychotherapeutic intervention for women receiving ante-natal and post-natal care at UCLH, their partners, and their children in the event of perinatal loss.
File results
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FOI/2023/0237 - Software solution to manage patient e-consent for school vaccinations/ immunisations and waitlist validation
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FOI/2023/0244 - IT systems for digital dictation, speech recognition, outsourced transcription, video consultation and health information systems
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FOI/2023/0247 - Treatment guidelines for Idiopathic Pulmonary Fibrosis
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FOI/2023/0242 - Treatment of Haemophilia A
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FOI/2023/0249 - Treatments for clotting disorders - Haemophilia B, Von Willebrand Disease
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FOI/2023/0260 - Treatment for rare diseases: Fabry, Gaucher and Pompe disease and Hunter Syndrome
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FOI/2023/0332 - Eating disorder services and Advance Decisions/ Directives to refuse medical treatment (ADRTs)
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FOI/2023/0262 - Clinical trial participation
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FOI/2023/0275 - Trust statistics on spiking
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FOI/2023/0360 - Minutes of Board of Director meetings and Declarations of Interests (DoI) statements 2008-2023