Page results
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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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A high quality diagnostic service for surgical neuropathology, neuromuscular diagnostics, epilepsy, molecular neuropathology of brain tumours, and neurodegenerative diseases.
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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 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 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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The department undertakes specialist dental treatment for those under 16 years of age ( 15 years and 11 months), and deals with the aetiology, prevention, diagnosis and treatment of oral disorders; mouth conditions and teeth of children.
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This page provides information for patients visiting the Inflammatory Bowel Disease clinic.
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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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This information outlines the things that you need to take home after your robotic prostatectomy.
File results
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FOI/2023/0025 - Surgical operating tables used in Trust
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FOI/2023/0037 - Assault attendances to Emergency Department
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FOI/2023/0038 - Cases where breast milk of a new mother was given to a child who is not her own
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FOI/2023/0041 - International recruitment
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FOI/2023/0054 - Local formulary used at the Trust
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FOI/2023/0058 - Skin cancer pathway management
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FOI/2023/0063 - Women who have given birth at the Trust aged 50 or above
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FOI/2023/0260 - Treatment for rare diseases: Fabry, Gaucher and Pompe disease and Hunter Syndrome
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FOI/2023/0249 - Treatments for clotting disorders - Haemophilia B, Von Willebrand Disease
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FOI/2023/0242 - Treatment of Haemophilia A