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Projects granted during 2016 that have a primary purpose of basic research, nervous system.
Projects granted during 2015 with a primary purpose of basic research: nervous system.
Projects granted during 2014 that have a primary purpose of basic research into the nervous system.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Explains how commissioners and health professionals can use data and analysis for decisions about neurology services and interventions.
Projects granted during 2016 that have a primary purpose of translational applied research - human nervous and mental disorders.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Projects granted during 2015 that have a primary purpose of translational and applied research: human nervous system and mental disorders.
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Information to assist with differentiating Lyme disease from other causes of rash, neurological or non-specific symptoms.
Information to assist with the laboratory diagnosis of Lyme disease and requirements for sample submission.
Guillain-Barré syndrome is a rare neurological condition which can occur following Zika virus infection.
UK Health Security Agency (UKHSA) culture collections offer a range of products and services for medical science and laboratory healthcare use.
Automation is the future for manufacturing stem cells, says the Head of the Medicines and Healthcare products Regulatory Agency’s UK Stem Cell Bank (UKSCB) on its 20th Anniversary.
Guidance for hospitals, tissue establishments and fertility clinics for ensuring the quality and safety of human organs, tissues and cells (including reproductive cells).
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Volume 34 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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