Page results
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Skeletal uscle 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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The spasticity service at NHNN offers a comprehensive, responsive multidisciplinary service to adults with spasticity associated with any neurological condition.
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Autoimmune serology is provided for: Connective tissue diseases, Endocrine diseases, Liver diseases, Rheumatic diseases, Skin diseases, Thyroid diseases.
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The Pathogen Genomic Unit offers access to explore the clinical applications and interpretation of pathogen genomic data for patients with a variety of infections.
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Dr Valeria Iodice is consultant in neurology and autonomic medicine and associate professor in neurology at University College London.
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This page aims to explain why the Shingles vaccine is being offered to you, how you can access the vaccine and any side effects or problems you may have.
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The molecular genetics laboratory at UCLH is a national centre for the genetic diagnosis of haemoglobin disorders, including prenatal diagnosis.
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The Virtual Arthroplasty Clinic Service at University College Hospital (UCH) offers high quality, safe and effective follow up care to patients after hip and/or knee replacement surgery.
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Bowel cancer is the third most common cancer in the UK and the second most common cause of cancer death. Screening helps to detect bowel cancer, or early signs of it, at an early stage and can prevent unnecessary deaths.
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UCLH's Haemostasis and thrombosis hub signposts patients to a range of services for blood disorders.
File results
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FOI/2023/0072 - Contact centre
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FOI/2023/0073 - Telephony and UC/ collaboration, Microsoft 365 licence and on-premise or cloud storage
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FOI/2023/0078 - Total loss written off in 2021/22
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FOI/2023/0088 - Appointments changed from in person to telephone due to industrial action
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FOI/2021/0284 - Sleep respiratory service
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FOI/2023/0099 - Number of autoclaves used at Trust
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FOI/2023/0101 - Trauma protocols in pregnant patients
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FOI/2023/0103 - Genetic Haemochromatosis patients
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FOI/2023/0117 - EPRR Team contact information
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FOI/2023/0125 - Staffing rota/ planning to support working parents