Page results
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The National Hospital for Neurology and Neurosurgery (NHNN) has one of the largest, most comprehensive programmes in Europe for the evaluation and medical and surgical treatment of epilepsy.
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The Headache Service provides advice and treatment to patients referred for the management of all headache disorders.
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Ms Nicola Lack has been a consultant obstetrician at UCLH since 2012 and has been the labour ward lead since 2019. She has a background in maternal medicine and works within the diabetes team.
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Our team deliver care to people with MS and aim to provide specialist services, share information on how to manage symptoms, offer education sessions, medication options and rehabilitation services.
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The Neurometabolic unit provides a unique range of investigations and clinical laboratory advice encompassing mitochondrial, neurotransmitter, pterin and amino acid disorders.
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The clinical management of neuromuscular muscle wasting diseases such as motor neuron disease, myasthenia gravis, muscular dystrophy and peripheral neuropathy.
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Typically, patient care is multidisciplinary led by consultant neuro-ophthalmologists and neurologists.
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The department is responsible for a wide range of neurophysiological procedures, principally electromyography (EMG) and nerve conduction studies, EMG-guided botulinum toxin (BoTox) injections, electroencephalography (EEG), evoked potentials (EPs) and intra-operative monitoring (IOM)
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Dr Tyagi is a consultant neuropsychiatrist with a special interest in Tourette's syndrome and obesessive compulsive disorders (OCD)
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The plasma exchange service at the National Hospital treats patients with neuroimmunological diseases such as Guillain-Barré syndrome and myasthenia gravis.
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