Page results
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Information about the integrated occupational therapy service at the Royal London Hospital for Integrated Medicine
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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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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 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 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 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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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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RESPOND is a new rapid access, community-based screening and care planning system for all asylum-seeking families registered with a GP in North Central London.
File results
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FOI/2023/0817 - Bed sores, pressure sores and pressure ulcers statistics
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FOI/2023/0822 - Bank staff pay rates
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FOI/2023/0827 - Consultation on future of EDS services
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FOI/2023/0829 - Immunoglobulin treatments
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FOI/2023/0831 - Treatments for acute myeloid leukaemia/ chronic lymphocytic leukaemia
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FOI/2023/0832 - Hospital admissions for vaping related disorders
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FOI/2023/0833 - Evaluation of outpatient referrals to neurosurgical department
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FOI/2023/0836 - Translation services and technologies
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FOI/2023/0837 - Treatment for Myelofibrosis
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FOI/2023/0840 - Deaths in accident and emergency 2018-2023