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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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 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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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.
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Find and Treat screen tens of thousands of the most vulnerable, homeless and high-risk people every year using mobile units deployed from UCLH.
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This patient information contains contraceptive advice for patients who have received Sugammadex.
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The molecular genetics laboratory at UCLH is a national centre for the genetic diagnosis of haemoglobin disorders, including prenatal diagnosis.
File results
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FOI/2024/0550 - Syntometrine vs Misoprostol/ treatment uses for post-partum haemorrhage
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FOI/2024/0559 - Surgical Robots purchase/ simulators/ procedures 2019-2024
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FOI/2024/0560 - Coroners' Prevention of Future Deaths Reports
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FOI/2024/0561 - Gender reassignment and/or transgender policies, mixed/same sex accommodation and Equality Impact Assessments (EIA)
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FOI/2024/0564 - Transperineal prostate biopsies undertaken in 2023
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FOI/2024/0568 - Local Anaesthetic Transperineal Prostate (LATP) biopsy service
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FOI/2024/0570 - Pathway for genetic/ genomic testing for MND
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FOI/2024/0573 - Treatment for haemophilia A and B/ von Willebrand patients
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FOI/2024/0575 - Replacement or purchase of patient trolleys in 2024/25
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FOI/2022/0780 - Hereditary Angioedema (HAE) service