Page results
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Advice on managing flare-ups and relapses for young people living with fatigue conditions.
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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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The molecular genetics laboratory at UCLH is a national centre for the genetic diagnosis of haemoglobin disorders, including prenatal diagnosis.
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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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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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The department specialises in the assessment and management of Complex Neuropsychiatric conditions occurring in the context of neurological disease.
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Information about the Integrated Cancer Care Service at UCLH
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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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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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This page explains what to do and what to avoid when your child has had extractions or minor oral surgery.
File results
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FOI/2022/0217 - Medications for dermatological conditions
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FOI/2022/0221 - Asthma medications
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FOI/2022/0223 - Policies/ procedures for management of patients with chest pain
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FOI/2022/0224 - Procurement for physiotherapy, occupational therapy, pharmacy, radiography, speech and language therapy and sterile services
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FOI/2022/0226 - Treatments for Haemophilia A
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FOI/2022/0227 - Number of cancer trackers and cancer MDT co-ordinators at Trust
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FOI/2022/0230 - Fabry, Gaucher and Pompe diseases drug treatments
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FOI/2022/0232 - Number of patients who have died while waiting for elective care
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FOI/2022/0233 - Diagnosis/ treatment of epilepsy, dravet syndrome, lennox gastaut syndrome and tuberous sclerosis complex
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FOI/2022/0236 - Video communication software licences